Genome-Wide Gene Expression Profiling of Fertilization Competent Mycelium in Opposite Mating Types in the Heterothallic Fungus Podospora anserina

被引:51
作者
Bidard, Frederique [1 ,2 ]
Benkhali, Jinane Ait [1 ,2 ]
Coppin, Evelyne [1 ,2 ]
Imbeaud, Sandrine [3 ]
Grognet, Pierre [1 ,4 ]
Delacroix, Herve [3 ]
Debuchy, Robert [1 ,2 ]
机构
[1] Univ Paris 11, Inst Genet & Microbiol, UMR8621, F-91405 Orsay, France
[2] CNRS, UMR8621, Inst Genet & Microbiol, F-91405 Orsay, France
[3] CNRS, Ctr Genet Mol, FRE3144, GODMAP, Gif Sur Yvette, France
[4] Univ Paris 07, UFR Sci Vivant, Paris, France
关键词
REAL-TIME PCR; PHEROMONE PRECURSOR GENES; NEUROSPORA-CRASSA; MITOCHONDRIAL GENOME; SORDARIA-MACROSPORA; GIBBERELLA-ZEAE; DNA-SEQUENCE; CELL-TYPE; PROTEIN; FERTILITY;
D O I
10.1371/journal.pone.0021476
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Background: Mating-type loci in yeasts and ascomycotan filamentous fungi (Pezizomycotina) encode master transcriptional factors that play a critical role in sexual development. Genome-wide analyses of mating-type-specification circuits and mating-type target genes are available in Saccharomyces cerevisiae and Schizosaccharomyces pombe; however, no such analyses have been performed in heterothallic (self-incompatible) Pezizomycotina. The heterothallic fungus Podospora anserina serves as a model for understanding the basic features of mating-type control. Its mat+ and mat- mating types are determined by dissimilar allelic sequences. The mat- sequence contains three genes, designated FMR1, SMR1 and SMR2, while the mat+ sequence contains one gene, FPR1. FMR1 and FPR1 are the major regulators of fertilization, and this study presents a genome-wide view of their target genes and analyzes their target gene regulation. Methodology/Principal Findings: The transcriptomic profiles of the mat+ and mat- strains revealed 157 differentially transcribed genes, and transcriptomic analysis of fmr1(-) and fpr1(-) mutant strains was used to determine the regulatory actions exerted by FMR1 and FPR1 on these differentially transcribed genes. All possible combinations of transcription repression and/or activation by FMR1 and/or FPR1 were observed. Furthermore, 10 additional mating-type target genes were identified that were up-or down-regulated to the same level in mat+ and mat- strains. Of the 167 genes identified, 32 genes were selected for deletion, which resulted in the identification of two genes essential for the sexual cycle. Interspecies comparisons of mating-type target genes revealed significant numbers of orthologous pairs, although transcriptional profiles were not conserved between species. Conclusions/Significance: This study represents the first comprehensive genome-wide analysis of mating-type direct and indirect target genes in a heterothallic filamentous fungus. Mating-type transcription factors have many more target genes than are found in yeasts and exert a much greater diversity of regulatory actions on target genes, most of which are not directly related to mating.
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