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Sex-linked transcriptional divergence in the hermaphrodite fungus Neurospora tetrasperma

In the filamentous ascomycete Neurospora tetrasperma, a large (approx. 7 Mbp) region of suppressed recombination surrounds the mating-type (mat) locus. While the remainder of the genome is largely homoallelic, this region of recombinational suppression, extending over 1500 genes, is associated with...

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Autores principales: Samils, Nicklas, Gioti, Anastasia, Karlsson, Magnus, Sun, Yu, Kasuga, Takao, Bastiaans, Eric, Wang, Zheng, Li, Ning, Townsend, Jeffrey P., Johannesson, Hanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3712418/
https://www.ncbi.nlm.nih.gov/pubmed/23782882
http://dx.doi.org/10.1098/rspb.2013.0862
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author Samils, Nicklas
Gioti, Anastasia
Karlsson, Magnus
Sun, Yu
Kasuga, Takao
Bastiaans, Eric
Wang, Zheng
Li, Ning
Townsend, Jeffrey P.
Johannesson, Hanna
author_facet Samils, Nicklas
Gioti, Anastasia
Karlsson, Magnus
Sun, Yu
Kasuga, Takao
Bastiaans, Eric
Wang, Zheng
Li, Ning
Townsend, Jeffrey P.
Johannesson, Hanna
author_sort Samils, Nicklas
collection PubMed
description In the filamentous ascomycete Neurospora tetrasperma, a large (approx. 7 Mbp) region of suppressed recombination surrounds the mating-type (mat) locus. While the remainder of the genome is largely homoallelic, this region of recombinational suppression, extending over 1500 genes, is associated with sequence divergence. Here, we used microarrays to examine how the molecular phenotype of gene expression level is linked to this divergent region, and thus to the mating type. Culturing N. tetrasperma on agar media that induce sexual/female or vegetative/male tissue, we found 196 genes significantly differentially expressed between mat A and mat a mating types. Our data show that the genes exhibiting mat-linked expression are enriched in the region genetically linked to mating type, and sequence and expression divergence are positively correlated. Our results indicate that the phenotype of mat A strains is optimized for traits promoting sexual/female development and the phenotype of mat a strains for vegetative/male development. This discovery of differentially expressed genes associated with mating type provides a link between genotypic and phenotypic divergence in this taxon and illustrates a fungal analogue to sexual dimorphism found among animals and plants.
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spelling pubmed-37124182013-08-07 Sex-linked transcriptional divergence in the hermaphrodite fungus Neurospora tetrasperma Samils, Nicklas Gioti, Anastasia Karlsson, Magnus Sun, Yu Kasuga, Takao Bastiaans, Eric Wang, Zheng Li, Ning Townsend, Jeffrey P. Johannesson, Hanna Proc Biol Sci Research Articles In the filamentous ascomycete Neurospora tetrasperma, a large (approx. 7 Mbp) region of suppressed recombination surrounds the mating-type (mat) locus. While the remainder of the genome is largely homoallelic, this region of recombinational suppression, extending over 1500 genes, is associated with sequence divergence. Here, we used microarrays to examine how the molecular phenotype of gene expression level is linked to this divergent region, and thus to the mating type. Culturing N. tetrasperma on agar media that induce sexual/female or vegetative/male tissue, we found 196 genes significantly differentially expressed between mat A and mat a mating types. Our data show that the genes exhibiting mat-linked expression are enriched in the region genetically linked to mating type, and sequence and expression divergence are positively correlated. Our results indicate that the phenotype of mat A strains is optimized for traits promoting sexual/female development and the phenotype of mat a strains for vegetative/male development. This discovery of differentially expressed genes associated with mating type provides a link between genotypic and phenotypic divergence in this taxon and illustrates a fungal analogue to sexual dimorphism found among animals and plants. The Royal Society 2013-08-07 /pmc/articles/PMC3712418/ /pubmed/23782882 http://dx.doi.org/10.1098/rspb.2013.0862 Text en http://creativecommons.org/licenses/by/3.0/ © 2013 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Research Articles
Samils, Nicklas
Gioti, Anastasia
Karlsson, Magnus
Sun, Yu
Kasuga, Takao
Bastiaans, Eric
Wang, Zheng
Li, Ning
Townsend, Jeffrey P.
Johannesson, Hanna
Sex-linked transcriptional divergence in the hermaphrodite fungus Neurospora tetrasperma
title Sex-linked transcriptional divergence in the hermaphrodite fungus Neurospora tetrasperma
title_full Sex-linked transcriptional divergence in the hermaphrodite fungus Neurospora tetrasperma
title_fullStr Sex-linked transcriptional divergence in the hermaphrodite fungus Neurospora tetrasperma
title_full_unstemmed Sex-linked transcriptional divergence in the hermaphrodite fungus Neurospora tetrasperma
title_short Sex-linked transcriptional divergence in the hermaphrodite fungus Neurospora tetrasperma
title_sort sex-linked transcriptional divergence in the hermaphrodite fungus neurospora tetrasperma
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3712418/
https://www.ncbi.nlm.nih.gov/pubmed/23782882
http://dx.doi.org/10.1098/rspb.2013.0862
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