Figures
Abstract
Using a screening protocol we have identified 68 genes that are required for female development in the filamentous fungus Neurospora crassa. We find that we can divide these genes into five general groups: 1) Genes encoding components of the PACC signal transduction pathway, 2) Other signal transduction pathway genes, including genes from the three N. crassa MAP kinase pathways, 3) Transcriptional factor genes, 4) Autophagy genes, and 5) Other miscellaneous genes. Complementation and RIP studies verified that these genes are needed for the formation of the female mating structure, the protoperithecium, and for the maturation of a fertilized protoperithecium into a perithecium. Perithecia grafting experiments demonstrate that the autophagy genes and the cell-to-cell fusion genes (the MAK-1 and MAK-2 pathway genes) are needed for the mobilization and movement of nutrients from an established vegetative hyphal network into the developing protoperithecium. Deletion mutants for the PACC pathway genes palA, palB, palC, palF, palH, and pacC were found to be defective in two aspects of female development. First, they were unable to initiate female development on synthetic crossing medium. However, they could form protoperithecia when grown on cellophane, on corn meal agar, or in response to the presence of nearby perithecia. Second, fertilized perithecia from PACC pathway mutants were unable to produce asci and complete female development. Protein localization experiments with a GFP-tagged PALA construct showed that PALA was localized in a peripheral punctate pattern, consistent with a signaling center associated with the ESCRT complex. The N. crassa PACC signal transduction pathway appears to be similar to the PacC/Rim101 pathway previously characterized in Aspergillus nidulans and Saccharomyces cerevisiae. In N. crassa the pathway plays a key role in regulating female development.
Citation: Chinnici JL, Fu C, Caccamise LM, Arnold JW, Free SJ (2014) Neurospora crassa Female Development Requires the PACC and Other Signal Transduction Pathways, Transcription Factors, Chromatin Remodeling, Cell-To-Cell Fusion, and Autophagy. PLoS ONE 9(10): e110603. https://doi.org/10.1371/journal.pone.0110603
Editor: Stefanie Pöggeler, Georg-August-University of Göttingen Institute of Microbiology & Genetics, Germany
Received: June 2, 2014; Accepted: September 16, 2014; Published: October 21, 2014
Copyright: © 2014 Chinnici et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: The authors confirm that all data underlying the findings are fully available without restriction. All of the data is available in the paper, in the supplemental materials, or on a website that is referenced within the paper.
Funding: Funding for this study was provided by National Institutes of Health Grant R01 GM078589 and by the University at Buffalo Foundation. The authors acknowledge the Neurospora Genome Project for the creation of the deletion mutants and the Fungal Genetics Stock Center for providing the mutants for their research efforts. Funding for the Neurospora Genome Project was provided by Grant #P01 GM068087 from the National Institutes of Health. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
From the viewpoint of a developmental biologist, the study of perithecial development in Neurospora crassa, and in the related ascomycetes Sordaria macrospora, Podospora anserina, and Gibberella zeae (anamorph Fusarium graminearum) has several advantages [1]. The morphological stages of perithecial development have been carefully cataloged by Lord and Read [2]. The perithecia is a reasonably simple structure with a limited number of different cell types [3]. Large numbers of perithecia can be generated and studied as they go through six days of development in a somewhat synchronous manner [4], [5]. The genomes of these ascomycetes have been sequenced [6], [7]. The expression pattern of the entire N. crassa genome has been examined by RNAseq during perithecia maturation [4]. Similarly, genome-wide expression patterns have been extensively analyzed during the development of S. macrospora and Gibberella zeae [5], [8], [9]. The organisms are haploid except during mating when a dikaryotic ascogenous tissue is generated and a diploid cell, which immediately undergoes meiosis, is formed. The haploid nature of the organisms facilitates the isolation and characterization of mutants affected in female development [1], [10]–[12]. Most importantly, the creation of the N. crassa single gene deletion library provides a unique opportunity to carry out a comprehensive genetic analysis of female development in a filamentous fungus [6], [13], [14].
The morphological events that occur during female development have been well documented in N. crassa, S. macrospora, P. anserina, and G. zeae [1], [2], [11], [15]–[21]. Female development can be initiated in N. crassa by nitrogen deprivation [22]. At the onset of female development a specialized coiled hyphal structure, called an ascogonium, is generated from a vegetative hypha. The ascogonium grows into a tightly woven spherically-shaped structure called a protoperithecium. The protoperithecium contains two types of cells, the ascogenous hyphae in the middle of the structure, and an outer layer of protective hyphae called the peridium. The ascogenous hyphae are generated from the ascogonium, but some of the hyphal elements of the peridium are thought to be generated by hyphae from the vegetative tissue that join with the ascogonium hyphae to create the protective outer layer. A long hypha, termed a trichogyne, is generated from the ascogenous hyphae and grows out of the protoperithecium. The trichogyne is attracted to a pheromone released by conidia and hyphae of the opposite mating type, and is able to undergo a cell fusion event with a cell of the opposite mating type to generate a dikaryon (a cell with two different types of nuclei) [23]. The pheromones and pheromone receptors that function in the chemotrophic growth of the trichogyne to a cell of the opposite mating type have been identified and characterized [24]–[27]. The movement of the male nucleus from the trichogyne into the ascogenous tissue, and the nuclear events within the ascogenous hyphae have been carefully characterized in N. crassa by Raju [23]. The male nucleus travels down the trichogyne into the ascogenous hyphae, where it undergoes several rounds of nuclear division. Hyphae having the shape of a “shepherd’s crook” (an upside down J) called crosiers, are generated within the ascogenous tissue. A single ascus cell containing a female and a male nucleus is generated at the top of the “crook” within each of these crosiers. Nuclear fusion occurs in the ascus cell, followed immediately by a meiotic division and a single mitotic division to generate a linear array of four pairs of nuclei. These then mature into eight ascospores. While the male nuclei are being replicated and ascospore formation occurs, the other cell types in the perithecium undergo development. The fertilized perithecium dramatically increases in size and becomes flask shaped. The outer layers of the peridium become highly melanized [10]. Specialized cells called paraphyses, which are thought to help support the development of the ascospores, are generated from the inner layer of the peridium and grow between the developing asci [2]. As perithecium development nears completion, an ostiolar pore (opening) is generated at the top of the flask-shaped perithecium. At the end of female development the mature ascospores are ejected through the ostiolar pore.
During the 1970 s, studies demonstrated that N. crassa female development was amenable to genetic analysis. Johnson [10] isolated a large number of mutants affected in female development and ordered these mutants based on the size of the developing protoperithecia. Vigfusson and Weiljer [28], Tan and Ho [29], and Mylyk and Thelkeld [30] also isolated female sterile mutants. Some of the mutations were mapped onto the N. crassa genetic map, while others were unmapped. Although these female developmental mutants were deposited in the Fungal Genetics Stock Center, only recently have any of the genes defined by these mutants been identified. Four of these “classical” female developmental genes, ff-1 (female fertile-1), fs-n (female sterile-n), ty-1/ste-50 (tyrosinaseless-1 or sterile-50), and per-1 (perithecial-1) were recently identified by whole genome sequencing of the mutant strains [31]. The ff-1 gene (NCU01543) encodes a LIM domain-containing protein with homology to Pat1p, a topoisomerase II-associated protein. The mutation in the fs-n strain was shown to be in the so/ham-1 gene (NCU02794), a WW domain-containing protein that has been shown to be needed for cell-to-cell fusion as well as for female development [32]. The per-1 mutation affects the melanization of the perithecia, and the mutant was initially identified by the presence of an unmelanized perithecia [33]. The per-1 gene (NCU03584) encodes a polyketide synthase, and probably functions in a melanin biosynthetic pathway. The ty-1/ste-50 mutant has a complex phenotype. It produces short aerial hyphae (flat conidiation), is female infertile, and is “tyrosinaseless” [34]. The ty-1/ste-50 gene (NCU00455) encodes a homolog of the S. cerevisiae Ste50 protein, a scaffold protein for the MAP kinase pathways.
In addition to a large number of N. crassa genes that have been identified as being needed for female development, many additional female development genes have been identified and characterized in S. macrospora, P. anserina, Magnaporthe grisea, and Aspergillus nidulans (see review by Pöggeler et al. [1]). These additional genes include transcription factors, signal transduction pathway proteins, and autophagy proteins, and provide a wealth of information on female development in filamentous fungi.
In this report, a morphological screening of the N. crassa single gene deletion library was used to identify the genes that are needed for the development of protoperithecia and their subsequent maturation into perithecia. In characterizing the mutants identified in this screening, we identified 68 genes that are needed for female development. One of the more interesting findings from the screening experiments was that the PACC signal transduction pathway is required for female development in N. crassa.
Results and Discussion
Isolation of protoperithecia-defective mutants and co-segregation experiments
To identify genes that are required for female development in N. crassa, a large-scale mutant screening experiment was carried out. As described in Materials and Methods, each of the 10,000 isolates in plates 1 to 119 of the N. crassa single gene deletion library was tested for the ability to produce protoperithecia and perithecia on a 3 ml slant of synthetic crossing medium (Figure 1). This screening was done in addition to our previous screening of the library to identify cell-to-cell fusion mutants, which were shown to be defective in protoperithecium development [35]. The purpose of the screening experiments described in this report was to identify other types of genes that are needed for female development. In these screening experiments we identified 649 mutants (representing 508 genes) that were either protoperithecia-defective or perithecia-defective. Co-segregation experiments were done for 443 of these genes. Co-segregation experiments were not done for most of the genes that encoded a known function not directly related to female development (genes important for mitochondrial ATP synthesis, ribosome functions, vesicular trafficking, etc.; see Table S1) and genes where the library contained two deletion isolates and only one of the isolates displayed the mutant phenotype. These co-segregation experiments showed that for 123 of the genes, the mutant phenotype co-segregated with the gene deletion, suggesting that the deletion might be responsible for the female-defective phenotype. Included in these genes were 31 genes that had been previously identified as being required for N. crassa female development (see Tables 1–3). This demonstrates that the screening and co-segregation experiments effectively identified genes that function in the process of female development. For 320 of the genes identified in the screening experiments, the co-segregation experiments showed that the female developmental defect did not co-segregate with the gene deletion, indicating that these mutants had additional mutations that were responsible for the mutant phenotype. Excel files showing the results of our screening, co-segregation, complementation, and RIP experiments can be accessed at our website (http://www.biology.buffalo.edu/Faculty/Free/KO_list_2014/KO_List.html).
Wild type, a ΔpalF isolate, and a ΔpalF isolate that has been transformed with a wild type copy of the palF gene were grown on 3 ml slants of SCM agar medium for 10 days to allow them to form protoperithecia. The three panels show images of the hyphae and protoperithecia on the test tube glass adjacent to the agar slant. An abundance of protoperithecia are produced by the wild type isolate on the glass at the edge of the agar (first panel/A) while the ΔpalF mutant is unable to produce protoperithecia (second panel/B). Transformation of the ΔpalF mutant with a wild type copy of the palF gene restores the ability to generate protoperithecia (third panel/C). Arrows point to examples of protoperithecia.
Among the mutants we identified in the screening experiment were several mutants that grew very poorly and had mutations in mitochondrial proteins, in general transcription proteins, in protein translation functions, in vesicular trafficking, and other “general cellular health” functions. Co-segregation experiments on a few of these mutants showed that the “general health” mutation did co-segregate with the female-defective phenotype. A list of these genes is found in Table S1, and, for the most part, these genes were not further characterized in our study. These mutants demonstrate that the hyphae must be “healthy” in order to participate in female development. We also noted that our experiments identified 18 genes that function in chromatin assembly and remodeling. The co-segregation experiments, along with some complementation experiments, clearly demonstrated that chromatin assembly and remodeling are required for female development. Others have previously shown chromatin assembly and remodeling mutants are defective in female development [36]–[39]. We have listed these chromatin organization genes in Table S2. Although a study of how chromatin remodeling is involved in directing female development is a very interesting topic, we did not focus on these mutants in our current study.
Complementation and RIP experiments
Complementation or RIP experiments were carried out on a majority of the putative female developmental genes defined by the co-segregation experiments. However, for some of the genes, pre-existing definitive information showing that the gene was required for N. crassa female development had been previously published, and complementation experiments were not carried out on these mutants. In these situations, the publication citation showing that the gene was needed for the protoperithecium development or maturation is provided in Tables 2 through 5. As described in Materials and Methods, the complementation experiments used wild type copies of the putative female developmental genes to transform the deletion mutants. The ability of the wild type gene to restore a wild type phenotype to a deletion mutant was taken as definite proof that the gene was needed for female development.
In cases where the complementation experiment was difficult because the mutant did not produce conidia, the cell type used in the transformation experiments, RIP experiments were used to generate additional mutated copies of the gene. In these cases, one or more of the RIP alleles were PCR amplified and sequenced to verify that the mutant allele(s) had multiple RIP mutations. As a result of our co-segregation, complementation, and RIP experiments, we identified 68 genes that are needed for female development. While many of these genes had been previously reported as being needed for female development, our studies identified 32 genes that had not been previously identified as being required for female development in N. crassa (denoted as being defined by this report in Tables 1 through 5). The results of our screening, cosegregation, and complementation experiments demonstrate the value of a careful screening of the N. crassa single gene deletion library in characterizing the biology of the model filamentous fungus. Our research also highlights the importance of using co-segregation and complementation experiments in verifying that the deletions identified in screening the deletion library give rise to the observed mutant phenotypes. As demonstrated by our study, the presence of secondary mutations in some isolates in the library does not detract from the value and importance of the single gene deletion library in analyzing N. crassa gene functions.
Cell-to-cell fusion assays
To further characterize our mutants, the ability of the mutants to participate in cell-to-cell fusion was assessed with the CAT fusion assay [40]. We and others have previously shown that cell-to-cell fusion is needed for female development [32], [35], [41], [42]. The genes required for cell-to-cell fusion are designated with an asterisk in Table 2. Interestingly, we found that all of the cell-to-cell fusion genes that we identified encode proteins that are either confirmed or likely participants in one of three closely related signaling pathways: 1) the STRIPAK signaling complex, which is required for the movement of MAK-1 into the nucleus in a MAK-2-dependent manner; 2) the MAK-1 cell wall integrity signal transduction pathway; and 3) the MAK-2 hyphal growth signal transduction pathway used to direct the growth of fusion hyphae towards each other [35], [43], [44].
Ascogonia formation
Female development begins with the formation of the ascogonium, a specialized coiled hyphae structure. To determine whether the mutants were affected in ascogonia formation, mutant conidia were used to inoculate either synthetic crossing medium with sucrose or cellophane filters placed on synthetic crossing medium (without an additional added carbon/energy source), and the formation of ascogonia was assessed under a compound microscope. The PACC pathway mutants (palA, palB, palC, palF, palH, and pacC) had a rather interesting ascogonia formation phenotype. We found that they were unable to produce ascogonia on the synthetic crossing medium with sucrose but were able to form ascogonia on cellophane.
In the ascogonia formation on cellophane experiments, we found that 17 of the mutants were affected in the formation of ascogonia. These included the mutants for the OS MAP kinase pathway gene os-2, os-4, and os-5 genes, which have been previously shown to be defective in ascogonia formation by Lichius et al. [45]. We also found that deletion mutants for the transcription factor rco-1 (NCU06205) and 3 calcium signaling genes, cnb-1 (NCU03833), camk-1 (NCU09123), and ham-10 (NCU02833) were affected in ascogonia formation. This suggests that Ca++ signaling may be required for the initiation of female development in N. crassa. Previous work on each of these genes has shown that they are needed for female development [46]–[48]. The other 10 genes affecting ascogonia formation were rac-1 (NCU02160), div-4 (NCU04426), stk-16 (NCU00914), stk-22 (NCU03523), stk-47 (NCU006685), fem-1 (NCU03589), fem-4 (NCU06243), fem-5 (NCU02073), fem-6 (NCU09052), and fem-7 (NCU03985). Most of these mutants produced an abundance of conidia instead of making ascogonia on the cellophane filter. These mutants also shared a second phenotypic characteristic, a hyper-production of conidia when grown on slants containing synthetic crossing medium with sucrose. We hypothesize that these genes may function in allowing the fungus to choose between two alternative developmental pathways, a sexual pathway leading to female development and the asexual pathway leading to conidiation. These genes may well define a signal transduction pathway needed for initiating female development.
Perithecium grafting experiments
Female development on synthetic crossing medium occurs in response to nitrogen limitation, a condition in which the fungus may be restricted in the synthesis of new amino acids, and need to rely on pre-existing amino acids for the synthesis of new proteins. We developed a perithecia grafting assay (see Materials and Methods) that allowed us to ask whether the vegetative hyphae from the mutants we identified in our screening experiments were able to support the development of newly fertilized wild type perithecia (Figure 2). The results of the perithecia grafting experiments were quite instructive. We found that deletion mutants for virtually all of the genes known to be needed for autophagy and deletion mutants for all of the genes known to be components of the MAK-1 and MAK-2 signal transduction pathways needed for cell-to-cell fusion were defective in supporting the development of wild type perithecia in these grafting experiments (Figure 2). This demonstrates that both autophagy and cell-to-cell fusion are needed within the vegetative hyphal network. We conclude that the release of amino acids, and perhaps other nutrients, from the vegetative hyphal network and the transferring of these nutrients into the developing perithecium are needed to support female development.
Small pieces of cellophane containing “graft” fertilized wild type protoperithecia were placed on mutant “host” vegetative hyphal networks grown on synthetic crossing medium. The “host” shown are: 1) Δfmf-1 (left panel/A) which shows a host supporting the development of the graft perithecia. 2) Δada-1 (middle panel/B) which shows a host not supporting the development of the graft perithecia. 3) ΔpalA (right panel/C) which shows the graft inducing protoperithecia in the ΔpalA host. Arrows point to examples of perithecia on the cellophane (left panel/A) and protoperithecia induced in the host vegetative hyphal network (right panel/C).
In doing the perithecia grafting experiments, we found that the mating types of the graft and host vegetative network had to be the same in order for the host to be able to support graft development, suggesting that the vegetative incompatibility system is operating between the host and graft tissues. In addition to providing an assessment of whether a mutant “host” supported a wild type “graft”, we noted a second unexpected phenomenon in the grafting experiments. When testing the PACC pathway mutants (palA, palB, palC, palF, palH, and pacC) as hosts, we found that the presence of wild type perithecia grafts of either mating type were able to induce protoperithecia formation in the host hyphal network surrounding the graft (Figure 2). We conclude that the PACC pathway operates to allow the fungus to choose the female developmental pathway in response to environmental/nitrogen limitation cues present in synthetic crossing medium. However, the fungus apparently has other pathways for inducing female development, and one of these pathways is responsive to the presence of nearby perithecia.
Functional grouping of the genes required for female development
An examination of the genes defined by the deletion mutants showed that we could assign the genes into five different categories. These were: 1) Genes encoding proteins which have been found to function in the PACC signal transduction pathway; 2) Genes encoding proteins that are likely to function in other signal transduction pathways, including the three N. crassa MAP kinase pathways, the STRIPAK pathway, the pheromone-responsive pathway, the NOX pathway, the heterotrimeric G protein signaling pathway, the septation initiation network (SIN), a Ca++ signaling pathway, and perhaps other signaling pathways; 3) Genes encoding probable transcription factors; 4) Genes that are required for autophagy; and 5) a few miscellaneous genes that don’t fit into the other categories. These genes are listed in Tables 1 through 5 respectively, along with details about the mutant phenotypes. To provide a somewhat comprehensive gene list, we have included a number of additional genes that have been shown by others to be involved in female development. In most of these cases, the deletion mutants for these genes weren’t identified in our screening experiments because they were not available in the library or they were found as heterokaryons in the library. These “added” genes include mfa-1(NCU06992), pre-1 (NCU00138), ccg-4 (NCU02500), pre-2 (NCU05758), asm-1 (NCU01414), fmf-1 (NCU09387), pp-1 (NCU00340), rho-1 (NCU01484), nor-1 (NCU07850), gna-1 (NCU06493), gng-1 (NCU00041), cnb-1 (NCU03833), cpc-2 (NCU05810), mcm-1 (NCU07430), per-1 (NCU03584), rgf-1 (NCU00668), rrg-1 (NCU01895), rcm-1 (NCU06842) and tyrosinase (NCU00776). Citations for the publications that demonstrated that these genes play roles in female development are included in Tables 2, 3, and 5. We will examine each category of mutants one at a time and describe their phenotypes and how they might function in supporting or directing female development.
Category #1: The PACC signal transduction pathway
The PacC/rim101 signal transduction pathway has been well characterized in A. nidulans and S. cerevisiae, where the pathway is regulated by the pH of the medium [49]–[53]. A representation of the pathway with the components we have identified in N. crassa is shown in Figure 3. In S. cerevisiae and A. nidulans, the pathway is activated at neutral-to-alkaline pHs, and the PACC protein functions as a transcription factor to activate expression of a number of genes needed for growth under neutral-to-alkaline pH conditions. The PALH protein, a seven transmembrane protein found in the plasma membrane, functions as the receptor or pH sensor for the pathway. PALH is found in a complex with the PALF protein, which has homology to arrestins. Under activating pH conditions, the PALF protein is phosphorylated and ubiquitinated. These modifications to PALF lead to the endocytosis of PALH protein, which joins with the PALA, PALB, PALC, and PACC proteins to create a multimeric signaling center within the ESCRT (endosomal sorting complexes required for transport) complex. Within the signaling center, PALB functions as a processing protease and cleaves an inhibitory C terminal domain from the PACC transcription factor. The activated PACC is released from the ESCRT complex and enters the nucleus. Since the PACC pathway has been characterized as a pH-dependent pathway, finding that it was required for female development in N. crassa, which occurs during nitrogen deprivation, was unexpected.
The PACC signal transduction pathway elements found in N. crassa, and the model for how the pathway might function are depicted. The PALH and PALF proteins are thought to be found at the plasma membrane. PALH is a seven transmembrane receptor which is sensitive to environmental cues. PALF is an arrestin type protein that associates with PALH. PALF is phosphorylated and ubiquitinated in response to the environmental cues. These events lead to the endocytosis of the PALH/PALF complex. Following endocytosis, the PALH is directed into an ESCRT compartment, where it enters into a signaling complex containing PALA, PALB, PALC, and PACC. Within the signaling complex, PALB functions as a protease which cleaves PACC. This cleavage event removes a C-terminal inhibitory domain from the PACC transcription factor, and the processed PACC is released from the signaling complex. The activated PACC then enters the nucleus and directs transcriptional activity leading to the formation of the protoperithecium.
We found that the ΔpalA, ΔpalB, ΔpalC, ΔpalF, ΔpalH, and ΔpacC mutants are all defective in protoperithecium development. We were unable to identify any ascogonia, the initial stage of protoperithecial development, when examining mutant hyphae growing on synthetic crossing medium, while ascogonia and protoperithecia were observed in wild type hyphae. Complementation analysis for these PACC pathway mutants verified that each of the genes was needed for protoperithecium formation (Figure 1, Table 1). The PacC pathway has been well-defined in A. nidulans, S. cerevisiae, and C. albicans as being required to regulate genes involved in growth in neutral-to-alkaline media [49]–[52], [54]–[60]. To the best of our knowledge, this is the first report demonstrating that the pathway is required for protoperithecial development. However, the PacC mutant of Sclerotinia sclerotium has been found to be defective in the formation of sclerotia, melanized structures that can remain dormant for many years and give rise to apothecia, the female structure for this species [61].
As noted in the ascogonia formation and perithecia graft experiments, the PacC pathway deletion mutants were unable to generate ascogonia and protoperithecia on synthetic crossing medium, but could produce protoperithecia in response to a signal from nearby fertilized perithecia from either mating type (Figure 2) or when grown of cellophane. We also tested for protoperithecia production on corn meal agar, a medium containing complex carbohydrates which can be used for N. crassa matings, and found that the PACC mutants produced protoperithecia on this medium. Our data shows that the PACC pathway is needed for the induction of female development (ascogonial development) only when female development is induced by growth on synthetic crossing medium, a medium that is generally ascribed as inducing female development in response to nitrogen deprivation, but that other environmental cues can induce female development in PACC pathway mutants. It is interesting to note that the environmental conditions inducing female development differ for different fungal species [1], which may reflect differences in their life cycles. We hypothesize that PACC induction of ascogonia production may be restricted to those fungi that induce female development in response to nitrogen limitation.
To determine whether the protoperithecia produced by PacC pathway deletion mutants were fully functional, we fertilized protoperithecia that had been induced by the presence of nearby perithecia or growth on corn meal agar. Upon fertilization, the mutant perithecia increased in size and began to melanize. However, the perithecia did not complete development and eject ascospores. Several of these mutant perithecia were examined, and we found that the perithecia did not grow as large as wild type perithecia. They also did not become as melanized as wild type perithecia. Microscopic examination of squashed mutant perithecia shows that they do not generate asci (Figure 4). Thus, we find that the PACC pathway is used at two different stages of female development, first during the initial induction of protoperithecial development in response to environmental cues, and then later in the maturing perithecia during the development of asci from the ascogenous tissue.
Fertilized perithecia from wild type (left panel/A) and ΔpalA (right panel/B) were allowed to develop for 7 days. The perithecia were squashed between a glass slide and a glass coverslip and examined with a transmitted light microscope. The wild type perithecia has generated ascospores (arrow) while the ΔpalA peirthecia is defective in ascospore formation. The arrow in the left panel points to an ascospore.
To determine whether the removal of the C terminal inhibitory domain of PACC was sufficient to direct N. crassa cells into the female developmental pathway, we prepared a version of pacC in which a stop codon was inserted into the gene at amino acid 492. The truncated protein made from this construct would lack the predicted inhibitory C terminus domain, and would be predicted to give rise to a constitutively active form of PACC. Transformation of wild type isolates with the plasmid encoding this constitutively active PACC resulted in the abundant formation of protoperithecia, even in the Vogel’s medium where female development is normally repressed. Transformants of the ΔpalA, ΔpalB, ΔpalC, ΔpalF, and ΔpalH with plasmid encoding the constitutive active form of PACC, also produced an abundance of protoperithecia (Figure 5). This demonstrates that PALA, PALB, PALC, PALF, and PALH are all upstream of PACC within the signaling pathway. We conclude that the activation of PACC is a major event in triggering female development in N. crassa, and that activation of PACC is sufficient to direct cells to undergo female development, even in the absence of the normal nitrogen limitation cue.
Cells were inoculated onto agar slants and allowed to grow for 10 days at room temperature. The left panel (A) shows a ΔpalC isolate on Vogel’s sucrose medium. The middle panel (B) shows a ΔpalC isolate that has been transformed with the constitutively activated PACC construct growing on synthetic crossing medium. The right panel (C) shows a ΔpalC isolate that has been transformed with the constitutively activated PACC construct growing on Vogel’s sucrose medium, a medium that represses female development. Note that the constitutively activated PACC caused protoperithecia production in the absence of PALC on both media. The arrows in the middle and right panels point to protoperithecia.
To examine whether the PACC pathway has the same characteristics in N. crassa that have been previously identified in the A. nidulans and S. cerevisiae systems, we decided to examine the intracellular location of PACC pathway components in wild type and mutant isolates. Endogenous promoter-driven GFP-tagged versions of PALA, PALC, and PALH were prepared using the pMF272 vector [62]. The GFP-tagged versions of PALC and PALH did not complement the deletion mutants and we were unable to detect a GFP signal, suggesting that the GFP-tagged proteins were rapidly degraded. However, the GFP-tagged PALA fully complemented the deletion mutation and gave a faint, but detectable intracellular signal in conidia and germlings. The faint signal was localized in a punctate pattern near the periphery of the conidia and germlings. We were unable to detect a signal from the GFP-tagged PALA within early developing protoperithecia (ascogenous coils), suggesting that the signal was weak. We also prepared a ccg-1 promoter-driven GFP-tagged PALA vector as described in Materials and Methods. Transformation with the ccg-1 promoter-driven GFP-tagged palA provided for a stronger signal in wild type and ΔpalA isolates (Figure 6). Examination of the GFP-tagged PALA in germinating conidia showed that the protein was localized in a punctate pattern near the cell surface. The data suggests that the N. crassa PACC pathway is localized to the ESCRT complex, just as was previously shown to occur for the A. nidulans and S. cerevisiae pathways [51], [52]. Our findings are consistent with the N. crassa PACC pathway functioning like the canonical PACC pathway defined in A. nidulans and S. cerevisiae. In S. cerevesiae, the PACC homlog, Rim101p, has been shown to be required for meiosis [55], [57], and the inability of the PACC pathway mutants to produce asci would suggest that the N. crassa PACC pathway may function in an analogous manner during the later stages of female development.
GFP-tagged PALA was expressed under the regulation of the ccg-1 promoter in a ΔpalA isolate. The GFP fluorescent image of a germling is shown in the panel on the left (A). The DIC image of the same germling is shown in the right panel (B). The bar in the DIC image is 10 µm in length.
Category #2: Genes encoding other signal transduction pathway elements
Table 2 lists 53 genes that are likely components of signal transduction pathways. An extensive analysis of the serine-threonine kinases encoded in the N. crassa genome was recently published, and many of the kinases we identify in Table 2 were also found to be defective in female development in that study [48]. Fourteen of these signal transduction pathway genes were previously defined as being required for cell-to-cell fusion in our previous study [35]. All three of the MAP kinase pathways encoded in N. crassa genome have been previously shown to be needed for female development [45]. Table 2 contains 25 genes required for the production of CATs (conidial anastomosis tubes), the cell type needed for cell-to-cell fusion. Most of these genes are known to be components of either the MIK-1/MEK-1/MAK-1 cell wall integrity pathway, the NRC-1/MEK-2/MAK-2 hyphal growth pathway, or the NOX pathway. These pathways have been identified as being needed for cell-to-cell fusion [32], [35], [45], [63], [64]. Table 2 contains three newly identified genes, pp-2A activator (NCU03269), whi-2 (NCU10518) and prs-1 (NCU08380), which are required for the CAT formation and are therefore likely components or regulators of the MAK-1 or MAK-2 pathways. The PP-2A activator (NCU03269) is likely associated with PP-2A (NCU06563), which has been shown to be a member of the STRIPAK complex that regulates the movement of MAK-1 into the nucleus [43]. WHI-2 is a homolog of a yeast general stress regulator [65]–[68]. Recent work in our laboratory has shown that MAK-1 and MAK-2 pathways are affected in the N. crassa whi-2 mutant [47]. PRS-1 is a putative membrane-associated protein phosphatase and forms a complex with WHI-2 [65]. In yeast, Whi2p and Psr1p have roles in autophagy and in responding to mitochondrial dysfunction [68]. Given the probable association between the PP2A activator and the STRIPAK complex and between PRS-1 and WHI-2, it seems likely that PP2A activator and PRS-1 are also involved in regulating the MAK-1 and MAK-2 pathways in N. crassa. Those signal transduction pathway components found in Table 2 that do not affect CAT formation are unlikely to be part of the MAK-1 and MAK-2 pathways, and are more likely to be functioning in some other pathway.
We noted that our list of signal transduction genes included the nox-1 (NCU02110) and nor-1 (NCU07850) genes, which function in superoxide production and signaling [69]–[71]. These genes have been previously identified by others as being needed for protoperithecia formation, and may play a key role in cell-to-cell signaling during female development [69], [72], [73].
The mfa-1 (NCU016992) and ccg-4 (NCU02500) pheromone genes and the genes encoding their receptors, pre-1 (NCU000138) and pre-2 (NCU005758), have been previously identified as playing vital functions during mating and perithecium maturation in N. crassa and S. macrospora [24], [27], [74]. The PRE-1 and PRE-2 receptors have been previously shown to function in directing growth of the trichogyne toward conidia of the opposite mating type to facilitate the fertilization event [27]. The signal transduction pathway(s) through which the PRE-1 and PRE-2 receptors function has not been characterized. Further analysis will be needed to characterize how this pathway functions.
Mutants that are affected in the process of septation formation have been previously shown to be unable to generate protoperithecia in S. macrospora and N. crassa [41], [75]–[77]. Our screening experiments corroborate the need for septation during female development. We identified cdc-7 (NCU01335), sid-1 (NCU04096), and dbf-2 (NCU09071) as being needed for protoperithecia formation (Table 2). Several other genes encoding components of the N. crassa sepatation initiation network (SIN) have been shown to needed for female development [76]–[80], but the deletion mutants were either absent from the single gene deletion library or found as heterokaryons, and these genes are not listed in Table 2.
Table 2 lists three genes involved in calcium signaling that were identified in our experiments. These are the gene for the calcineurin subunit b, cnb-1 (NCU03833), the calcium/calmodulin-dependent protein kinase camk-1 (NCU09123), and ham-10 (NCU02833), which encodes a C2 domain-containing protein. C2 domains are thought to function as calcium-dependent lipid-binding domains involved in vesicular trafficking. All three of these genes have been previously identified as affecting female development [46]–[48].
In addition to the components of the three MAP kinase pathways, the PACC pathway, the NOX-1 pathway, the septation initiation network, the pheromone pathway, and the calcium signaling pathway, Table 2 also contains five additional kinases. These kinases are fi (NCU04990), div-4 (NCU04426), stk-16 (NCU00914), stk-22 (NCU03523), and stk-47 (NCU06685). Four of these kinases, div-4, stk-16, stk-22 and stk-47 are needed for ascogonia formation, and may be part of a signaling pathway regulating entry into female development. However, further work is needed to characterize how these kinases function during protoperithecia formation and maturation.
Category #3: Transcription factors
Table 3 lists the 10 transcription factor genes that we have identified as being needed for female development. Although not listed in Table 3, the genes at the two mating alleles encode transcription factors that have been well characterized and are known to play critical roles in regulating transcriptional activity during female development [81]. In P. anserina, a group of ten HMG-box proteins, including the mating type proteins, have been shown to function in directing perithecial development [82], [83]. Except for pacC, all of the transcription factors in Table 3 have been previously identified as being involved in female development by others [84]. The asm-1 (NCU01414) transcription factor was previously identified by Aramayo et al. [85] as being needed for protoperithecium development. The rco-1 (NCU06205), rcm-1 (NCU06842) and adv-1 (NCU07392) genes had been previously identified as encoding transcription factors needed for cell-to-cell fusion [35]. The rco-1 (NCU06205) and rcm-1 (NCU06842) genes are homologs of the S. cerevisiae SSN6 and TUP1genes, which encode the subunits of a general dimeric transcription factor. RCO-1 and RCM-1 have been previously identified as being needed for female development [86]. ADV-1 is a homolog of the S. macrospora PRO-1 protein, which has been shown to be needed for female development [87], [88]. The ada-1 (NCU00499) and adv-1 (NCU07392) genes were identified as transcription factors needed for both asexual and sexual development [84], and we verified their importance for female development by complementation experiments. The fmf-1 (NCU09387) gene was previously characterized by Iyer et al. [89] as a homolog of the S. pombe Ste11p, a transcription factor involved in the expression of genes involved in pheromone signaling. Hutchinson and Glass [90] previously reported that the fsd-1 (NCU09915) gene was needed for the transition from protoperithecium to a mature perithecium. The pp-1 (NCU00340) and pacC (NCU00090) genes encode transcription factors that are known to function in the MAK-2 and PACC signal transcription pathways [51], [52], [91], [92]. In addition to these transcription factors that had been previously identified and characterized in N. crassa, one additional transcription factor for female development, MCM-1 (NCU07430) is listed in Table 3. The deletion mutant for mcm-1 is not found in the first 119 plates of the library, but a mcm-1 mutant has been characterized in the closely related S. macrospora and shown to be unable to produce perithecia [93], [94]. The S. macrospora MCM-1 has been shown to associate with a protein encoded by the mating type locus gene, and to regulate gene expression during perithecium development [93].
Category #4: Autophagy genes
The identification of 10 genes in our screening and co-segregation experiments that are required for autophagy (Table 4), clearly demonstrates that autophagy is a required activity during female development. Previous work from the Pöggeler laboratory has demonstrated the importance of autophagy during S. macrospora female development [95]–[98]. The atg-4, atg-7, atg-8, vps-34 and vps15 genes have each been shown to be required for perithecial development in S. macrospora. Autophagy has been studied in Magnaporthe oryzae, where it has been shown to be important for asexual development, perithecial development, and appressorium formation [99], [100]. In Aspergillus oryzae, the deletion of autophagy genes was shown to affect the conidiation process [101]. Complementation experiments with 2 of our autophagy genes, atg-3 and atg-8, verified that autophagy was required for the development of N. crassa protoperithecia. Some of our autophagy mutants were initially identified as being protoperithecia-defective while others were identified as being perithecia-defective. However, careful examination of the autophagy mutants shows that these mutants can initiate female development (produce ascogonia) and make a few small protoperithecia. Thus, the autophagy mutants might be best described as being able to initiate protoperithecium development, but unable to fully support subsequent female development. The protoperithecia grafting experiments demonstrate that autophagy is required within the vegetative hyphal network. We found that fertilized autophagy mutant perithecia were able to complete female development and produced ascospores when grafted onto a wild type host. We conclude that the autophagy mutants are affected in female development because the vegetative hyphal network is unable to provide an adequate supply of nutrients to the developing female.
Category #5: Miscellaneous genes
There were 10 genes that are required for female development which didn’t fall into one of the 4 categories discussed above (Table 5). Among the miscellaneous genes we identified as being needed for female development were 3 genes that were annotated as encoding enzymes that are likely to function in melanin biosynthesis. Tyrosinase, which is encoded by the T gene (NCU00776), catalyzes the formation of melanin from dihydroxyphenylalanine (DOPA), and has been previously shown to be needed for protoperithecia formation [102]. In addition to tyrosinase, the per-1 gene (NCU03584), which encodes a polyketide synthase that is probably needed for the production of melanin from dihydroxynapthalene (DHN), is needed for perithecium melanization. The Δper-1 mutant has an unmelanized perithecia phenotype [31]. We also found that an aldo-keto reductase gene (NCU01703) was needed for female development. The aldo-keto reductase may function in the pathway with the polyketide synthase for the production of DHN melanin. A polyketide synthase gene cluster has also been shown to be important for S. macrospora perithecial development [103], [104].
Table 5 lists 7 genes that were annotated as encoding “hypothetical proteins” or “conserved hypothetical proteins” in the N. crassa genome site at the Broad Institute website. These genes have been verified by complementation as being needed for female development (Table 5). We have named these genes as fem genes to designate that they are required for female development. Some of the encoded hypothetical proteins are highly conserved in the genomes of the filamentous fungi, suggesting that the genes play important roles in the life cycles of the filamentous fungi. As mentioned in the ascogonia formation section, fem-1, fem-4, fem-5, fem-6, and fem-7 may function with the div-4, stk-16, stk-22 and stk-47 kinases in a signal transduction pathway regulating the choice between asexual and sexual developmental programs. As the annotation of the N. crassa genome improves and further research is done, we hope that we will be able to identify functions for many of these conserved hypothetical proteins.
Conclusions
Our research demonstrates that a rather large number of signal transduction pathways and transcription factors are required to regulate female development (Tables 1, 2 and 3). Our analysis, in conjunction with other previously published studies, points to the involvement of at least nine different signal transduction pathways regulating female development. These are: 1) the MIK-1/MEK-1/MAK-1 cell wall integrity MAP kinase pathway; 2) the HAM-2/HAM-3/HAM-4/MOB-3 striatin pathway involved in making a complex on the nuclear envelope and in directing the movement of MAK-1 into the nucleus in a MAK-2 dependent manner; 3) the NRC-1/MEK-2/MAK-2 hyphal growth MAP kinase pathway; 4) the OS-2/OS-4/OS-5 osmotic stress MAP kinase pathway; 5) the NOX-1/NOR-1 superoxide pathway; 6) the PRE-1/PRE-2 pheromone signal transduction pathway; 7) the septation initation network (SIN), 8) a calcium signaling pathway, and 9) the PACC signal transduction pathway, which functions during the induction of protoperithecium development and during the maturation of the perithecium. Our experiments suggest that there is a signaling pathway that regulates the choice between sexual development and asexual development, and points to several genes that are likely to function in the pathway. We also found that chromatin remodeling was needed for female developments. Our experiments highlighted the role of autophagy and cell-to-cell fusion in the neighboring vegetative hyphae, which functions to provide nutrients to the developing female. What is clear from the analysis is that female development requires the coordinated activities of a number of signaling pathways.
Materials and Methods
Strains and growth conditions
Strains were routinely grown on Vogel’s minimal medium with 2% sucrose or on synthetic crossing medium with 0.5% sucrose [22]. The single gene deletion library was obtained from the Fungal Genetics Stock Center (Kansas City, MO). The ΔpacC mutant was a kind gift from Dr. Maria Bertolini (Sao Paulo, Brazil) [92]. To provide the strains needed for the complementation experiments with the pBM60/pBM61 vector system, deletion mutants were mated with a his-3 mutant of the opposite mating type (his-3, mat-A FGSC#6103 or a his-3, mat-a isolate obtained by mating FGSC#6103 with wild-type mat-a) and his-3 isolates containing the deletion mutation were isolated from among the progeny. These mating experiments were carried out as described in Davis and DeSerres [22].
To determine whether mutant isolates could form ascogonia, cellophane filters overlaid on synthetic crossing medium (without carbon/energy supplementation) were inoculated with conidia. Two to three days post-inoculum, pieces of cellophane were cut from the filters and the presence of ascogonia was assessed by observation under a compound microscope at 200 X magnification. Ascogonia formation was also assessed by inoculating synthetic crossing medium containing 0.1% sucrose with conidia and allows the cells to grow for one to three days. Agar samples were then removed from the culture and examined for ascogonia under the compound microscope.
Screening the library
A screening procedure was used to identify mutants in the Neurospora deletion library that were defective in the formation of protoperithecia or for their subsequent development into mature perithecia. Plates 1 through 119 of the library contain approximately 10,000 haploid deletion mutants. Each of these mutants was individually inoculated into a glass test tube (16 × 100 mm) containing a 3 ml synthetic crossing medium agar slant. The isolates were allowed to grow for 10 days at room temperature, and examined for the presence of protoperithecia under the dissecting microscope. Protoperithecia were readily observed on the glass test tube near the edge of the synthetic crossing medium (Figure 1). After screening for protoperithecia formation, we added approximately 500 µl of water containing conidia of both mat-A and mat-a mating types to each of the slants to fertilize the protoperithecia and induce perithecium development. The slants were visually screened for the development of melanized perithecia three to four days after adding the conidial suspension. The haploid mutants isolated by the screening procedure would be considered as maternal or female developmental mutants. Most of the deletion mutants were tested for complementation in heterokaryons, and the deletion mutations found to be recessive.
Co-segregation analysis
Many of the isolates in the N. crassa single gene deletion library have mutations in addition to the targeted deletion [35]. To help determine if the deletion mutations were responsible for the protoperithecium-defective and perithecium-defective phenotypes observed in the screening procedure, the mutants were subjected to a co-segregation analysis. The mutants were mated with a wild type isolate of the opposite mating type and ascospore progeny from these matings were collected [22]. Because all of the mutants were defective in female development, the mutant isolates were used as the conidial (male) partners in these matings. Ascospores from each of the matings were activated and 24 single ascospore progeny were isolated using standard procedures [22]. Each of the progeny were tested for hygromycin resistance and for the ability to form protoperithecia or perithecia with the same procedure used in the initial screening. The deletion mutations are marked by the insertion of the hygromycin resistance cassette in replacement of the deleted gene [84]. The co-segregation of hygromycin resistance with the mutant phenotype was taken as preliminary evidence that the deletion mutation was responsible for the mutant phenotype. The mutant phenotype was ascribed to a mutation other than the deletion in those cases where the mutant phenotype did not co-segregate with hygromycin resistance.
Many of the deletion mutations are represented by two isolates in the single gene deletion library, one of each mating type. In screening the library for protoperithecia-defective and perithecia-defective mutants, we found several cases where only one of the two deletion isolates in the library was defective in female development. Prior experience doing co-segregation analysis with the library showed that in such cases, the mutant phenotype invariably does not co-segregate with the deletion mutation [35]. Thus, the phenotype was assumed to be due to a mutation other than the deletion in those cases where the library contained two isolates and only one of the isolates had a mutant phenotype.
Cell-to-cell fusion assays
A number of the previously characterized cell-to-cell fusion (anastomosis) mutants have been previously shown to be affected in female development [32], [35], [42], [45], [105]. To identify cell-to-cell fusion mutants among the mutants affected in female development, the mutants were individually tested for the ability to participate in cell-to-cell fusion with the conidial anastomosis tube fusion (CAT fusion) assay as previously described by Fu et al. [35]. The CAT fusion assay was originally described and developed by Roca et al. [40].
Perithicia grafting experiments
The primary purpose of the protoperithecia grafting experiments was to determine whether a mutant vegetative hyphal network could support the development of transplanted wild type perithecia. A P. anserina perithecia grafting technique, which consists of transferring perithecia directly onto a host hyphal network has been previously described [106], [107]. In using this technique with N. crassa, we found that complementation between a wild type graft and a mutant host resulted in the production of multiple perithecia at the graft site. It was very difficult to differentiate between the grafted perithecia and perithecia produced by complementation within the mutant host hyphae. We therefore used a modification of the Podospora grafting techniques to evaluate N. crassa female development. To perform the grafting experiments, mutant isolates were grown on an agar plates containing SCM with 0.5% sucrose for ten days to provide “hosts” for the grafted perithecia. Wild type isolates were grown for 10 days at room temperature on a cellophane filters that had been overlaid on Petri dishes containing SCM with 0.5% sucrose agar medium. An abundance of wild type protoperithecia developed on the cellophane. A conidial suspension of the opposite mating type was then used to fertilize these wild type protoperithecia. Twenty four hours after fertilization, small pieces of cellophane (approximately 0.5 cm squares) with fertilized “graft” perithecia were cut from the filter with a sterilized new razor blade and transferred onto the Petri dishes containing mutant “host” vegetative hyphae. Three or four small pieces of cellophane containing fertilized wild type perithecia were transferred to each “host” Petri dish (Figure 2). The ability of the mutant vegetative hyphae to support development of the “graft’ wild type fertilized perithecium was determined by whether or not the perithecia on the cellophane filter ripened and shot ascospores.
In doing these grafting experiments, we determined that the host and graft had to be of the same mating type in order for the host to support perithecial development in the graft, suggesting that the vegetative incompatibility phenomenon was operative during the grafting experiments. This is in contrast with the P. anserina grafting experiments, in which hosts of either mating type could sustain the development of the grafted perithecia [106].
The perithecia grafting experiments allowed us to evaluate two different aspects of female development. First and foremost, they allowed us to determine whether a mutant host vegetative hyphal network could support the development of fertilized graft perithecia of the same mating type. Second, we found that grafted wild type perithecia could induce protoperithecia formation in a vegetative hyphal network of some of our mutants.
Cloning, complementation, and RIP analysis
Complementation experiments were used to definitely demonstrate that a gene identified in the deletion library was required for female development. These complementation experiments were carried out with the pBM60/pBM61 cloning system as previously described [35]. To test for complementation, PCR primers were used to amplify the putative female development genes along with approximately 1500 base pairs of upstream sequence and 500 base pairs of downstream sequence, and the genes were cloned into the pBM60 and pBM61 vectors [108]. The primers were designed so that they contained restriction enzyme sites that allowed for the cloning of the genes into a multicloning site in the plasmids. The primers used in cloning the PACC pathway genes are given in Table S3. The pBM60 and pBM61 vectors are designed for the targeted insertion of plasmid sequences into the intergenic region downstream of the his-3 locus. pBM60 or pBM61-derived plasmids for each of the cloned genes were used to transform an isolate having the gene deletion in a his-3 background. Insertion of the plasmid sequences by homologous recombination generated a wild-type copy of the his-3 gene, and allowed for the isolation of the transformant. Several transformants for each of the cloned genes were isolated and tested for the ability to make protoperithecia or perithecia on 3 ml slants of synthetic crossing medium. The ability of the cloned wild type gene to complement the deletion mutation was taken as definite proof that the gene was needed for female development.
For those mutants that did not produce conidia, the cell type used in the transformation experiments for the complementation analysis, we carried out RIP (repeat induced point mutation) analyses to verify that the mutant phenotype was due to the mutation of the targeted gene. RIP is a phenomenon in which genes that are present in two or more copies in a haploid genome are extensively mutated during the N. crassa sexual cycle [109]. Both copies of a duplicated gene receive multiple C to T (G to A) mutations during the RIP process. The RIP experiments were performed by cloning genes into the pBM60 or pBM61 as described above. The plasmids were used to transform his-3 conidia to generate a strain having two copies of the cloned gene. These transformants were then mated with a his-3 strain of the opposite mating type to activate the RIP process. Individual his-3 progeny with the mutant phenotype were then isolated. Being his-3 isolates, these progeny will have a single copy of the gene in question (they don’t have the “second copy” of the gene which was targeted into the his-3 locus during the transformation). The gene was then PCR amplified and sequenced to determine if the mutant phenotype was the result of RIP mutations within the gene.
Constitutively activated version of PACC
A constitutively activated version of PACC was created by introducing a stop codon into the pacC gene. The stop codon was placed such that the encoded protein lacked the C terminal 129 amino acids. This construct was generated by using the Gibson Assembly Master Mix kit (New England BioLabs, Ipswich, MA). Primers pacC-F and pacC-activated-R (Table S3) were used to amplify the 5′UTR and pacC coding region through the added stop codon region. Primers pacC-activated-F and pacC-R (Table S3) were used to amplify the region beginning with the stop codon and containing 3′ UTR sequences. The two PCR products were mixed with XbaI and EcoRI digested pBM60 and the Gibson Assembly Master Mix to generate a full length pacC containing the early stop codon.
Intracellular localization of GFP-tagged PALA
Two versions of GFP-tagged PALA were generated to examine the localization of PALA in wild type and mutant backgrounds. Both versions were created in the pMF272 vector [62] and contain the complete PALA coding region followed by the GFP coding sequence. The two versions differed in the promoter region used to drive expression of the protein. One of the versions contained the ccg-1 promoter found in pMF272 to drive high level expression of PALA, while the other version contained the normal palA promoter. For the palA promoter version, PCR primers palA-GFP-F and palA-GFP-R (Table S3) were used to amplify the region from 1374 base pairs upstream of the coding region to the amino acid preceding the stop codon for PALA. The PCR primers contained restriction enzyme sites to facilitate the cloning of the amplified gene and its upstream regulatory sequence immediately preceding, and in frame with, the GFP sequences in pMF272. To construct the ccg-1 promoter version of pal-A, primers pal-GFP-ccg-1-F and palA-GFP-ccg-1-R (Table S3) were used to amplify and clone the coding region of palA into pMF272. The pMF272 vector is designed to facilitate the insertion of the cloned sequences into the intergenic region downstream of the his-3 gene by homologous recombination [62]. The GFP-tagged palA plasmid constructs were used to transform the ΔpalA, his-3 mutant to demonstrate by complementation that the GFP-tagged PALA was fully functional. The location of the GFP-tagged PALA was assessed by fluorescence confocal microscopy. Similar GFP tagging experiments were carried out to produce GPF versions of PALC and PALH, but these GFP-tagged proteins failed to complement their deletion mutants.
Supporting Information
Table S1.
List of protoperithecia defective/deficient mutants where the gene deletion is likely to be causing the phenotype because of general cellular health problems. Genes that function in general metabolic pathways needed for female development are listed along with their NCU numbers. For those genes where co-segregation and complementation experiments were done to verify that the genes were needed for female development, the information is provided in the co-segregation and complementation column. Information about the type of encoded protein and the general metabolic functions it is involved in are given in the notations and protein function columns.
https://doi.org/10.1371/journal.pone.0110603.s001
(DOCX)
Table S2.
Chromatin organization genes required for female development. The genes identified in the screening procedure as being involved in generating and remodeling chromatin are listed. The deletion mutations that were shown to co-segregate with the female developmental phenotype are noted with a “yes” in the co-segregation column. Those genes that we verified as being required for female development by complementation are noted with a “yes” in the complementation column. The designation of PP in the complementation column indicates that previously published information demonstrates that the gene is needed for female development, and the reference for the information is given in the reference information column.
https://doi.org/10.1371/journal.pone.0110603.s002
(DOCX)
Table S3.
Primers used in cloning PACC pathway genes. The primers used for PCR amplification and cloning of the PACC pathway genes are listed. The added restriction sites used for inserting the genes into pMB60 and pMB61 are underlined. The pacC-F, pacC-R, pacC-activated-F, and pacC-activated-R were used with the Gibson cloning kit to introduce a stop codon into the pacC gene.
https://doi.org/10.1371/journal.pone.0110603.s003
(DOCX)
Acknowledgments
We acknowledge the Neurospora Genome Project for the creation of the deletion mutants and the Fungal Genetics Stock Center for providing the mutants for our research efforts. We thank James Stamos for help in the preparation of the manuscript and Alan Siegel for help with fluorescence microscopy. We also thank Zhao Na, Amanda Lickfield, Yichen Li, and Genessis Capellan for their assistance with screening, co-segregation, complementation, RIP, and grafting experiments.
Author Contributions
Conceived and designed the experiments: JLC CF LMC JWA SJF. Performed the experiments: JLC CF LMC JWA SJF. Analyzed the data: JLC CF LMC JWA SJF. Contributed reagents/materials/analysis tools: JLC CF LMC JWA SJF. Contributed to the writing of the manuscript: JLC CF SJF.
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