Cargando…
Evolutionarily Diverged Regulation of X-chromosomal Genes as a Primal Event in Mouse Reproductive Isolation
Improper gene regulation is implicated in reproductive isolation, but its genetic and molecular bases are unknown. We previously reported that a mouse inter-subspecific X chromosome substitution strain shows reproductive isolation characterized by male-specific sterility due to disruption of meiotic...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3990516/ https://www.ncbi.nlm.nih.gov/pubmed/24743563 http://dx.doi.org/10.1371/journal.pgen.1004301 |
_version_ | 1782312292852957184 |
---|---|
author | Oka, Ayako Takada, Toyoyuki Fujisawa, Hironori Shiroishi, Toshihiko |
author_facet | Oka, Ayako Takada, Toyoyuki Fujisawa, Hironori Shiroishi, Toshihiko |
author_sort | Oka, Ayako |
collection | PubMed |
description | Improper gene regulation is implicated in reproductive isolation, but its genetic and molecular bases are unknown. We previously reported that a mouse inter-subspecific X chromosome substitution strain shows reproductive isolation characterized by male-specific sterility due to disruption of meiotic entry in spermatogenesis. Here, we conducted comprehensive transcriptional profiling of the testicular cells of this strain by microarray. The results clearly revealed gross misregulation of gene expression in the substituted donor X chromosome. Such misregulation occurred prior to detectable spermatogenetic impairment, suggesting that it is a primal event in reproductive isolation. The misregulation of X-linked genes showed asymmetry; more genes were disproportionally downregulated rather than upregulated. Furthermore, this misregulation subsequently resulted in perturbation of global transcriptional regulation of autosomal genes, probably by cascading deleterious effects. Remarkably, this transcriptional misregulation was substantially restored by introduction of chromosome 1 from the same donor strain as the X chromosome. This finding implies that one of regulatory genes acting in trans for X-linked target genes is located on chromosome 1. This study collectively suggests that regulatory incompatibility is a major cause of reproductive isolation in the X chromosome substitution strain. |
format | Online Article Text |
id | pubmed-3990516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39905162014-04-21 Evolutionarily Diverged Regulation of X-chromosomal Genes as a Primal Event in Mouse Reproductive Isolation Oka, Ayako Takada, Toyoyuki Fujisawa, Hironori Shiroishi, Toshihiko PLoS Genet Research Article Improper gene regulation is implicated in reproductive isolation, but its genetic and molecular bases are unknown. We previously reported that a mouse inter-subspecific X chromosome substitution strain shows reproductive isolation characterized by male-specific sterility due to disruption of meiotic entry in spermatogenesis. Here, we conducted comprehensive transcriptional profiling of the testicular cells of this strain by microarray. The results clearly revealed gross misregulation of gene expression in the substituted donor X chromosome. Such misregulation occurred prior to detectable spermatogenetic impairment, suggesting that it is a primal event in reproductive isolation. The misregulation of X-linked genes showed asymmetry; more genes were disproportionally downregulated rather than upregulated. Furthermore, this misregulation subsequently resulted in perturbation of global transcriptional regulation of autosomal genes, probably by cascading deleterious effects. Remarkably, this transcriptional misregulation was substantially restored by introduction of chromosome 1 from the same donor strain as the X chromosome. This finding implies that one of regulatory genes acting in trans for X-linked target genes is located on chromosome 1. This study collectively suggests that regulatory incompatibility is a major cause of reproductive isolation in the X chromosome substitution strain. Public Library of Science 2014-04-17 /pmc/articles/PMC3990516/ /pubmed/24743563 http://dx.doi.org/10.1371/journal.pgen.1004301 Text en © 2014 Oka et al http://creativecommons.org/licenses/by/4.0/ 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 properly credited. |
spellingShingle | Research Article Oka, Ayako Takada, Toyoyuki Fujisawa, Hironori Shiroishi, Toshihiko Evolutionarily Diverged Regulation of X-chromosomal Genes as a Primal Event in Mouse Reproductive Isolation |
title | Evolutionarily Diverged Regulation of X-chromosomal Genes as a Primal Event in Mouse Reproductive Isolation |
title_full | Evolutionarily Diverged Regulation of X-chromosomal Genes as a Primal Event in Mouse Reproductive Isolation |
title_fullStr | Evolutionarily Diverged Regulation of X-chromosomal Genes as a Primal Event in Mouse Reproductive Isolation |
title_full_unstemmed | Evolutionarily Diverged Regulation of X-chromosomal Genes as a Primal Event in Mouse Reproductive Isolation |
title_short | Evolutionarily Diverged Regulation of X-chromosomal Genes as a Primal Event in Mouse Reproductive Isolation |
title_sort | evolutionarily diverged regulation of x-chromosomal genes as a primal event in mouse reproductive isolation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3990516/ https://www.ncbi.nlm.nih.gov/pubmed/24743563 http://dx.doi.org/10.1371/journal.pgen.1004301 |
work_keys_str_mv | AT okaayako evolutionarilydivergedregulationofxchromosomalgenesasaprimaleventinmousereproductiveisolation AT takadatoyoyuki evolutionarilydivergedregulationofxchromosomalgenesasaprimaleventinmousereproductiveisolation AT fujisawahironori evolutionarilydivergedregulationofxchromosomalgenesasaprimaleventinmousereproductiveisolation AT shiroishitoshihiko evolutionarilydivergedregulationofxchromosomalgenesasaprimaleventinmousereproductiveisolation |