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...

Full description

Bibliographic Details
Main Authors: Ayako Oka, Toyoyuki Takada, Hironori Fujisawa, Toshihiko Shiroishi
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-04-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC3990516?pdf=render
id doaj-c779f91e5de74b439d60a9a63c4846a4
record_format Article
spelling doaj-c779f91e5de74b439d60a9a63c4846a42020-11-25T00:15:14ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042014-04-01104e100430110.1371/journal.pgen.1004301Evolutionarily diverged regulation of X-chromosomal genes as a primal event in mouse reproductive isolation.Ayako OkaToyoyuki TakadaHironori FujisawaToshihiko ShiroishiImproper 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.http://europepmc.org/articles/PMC3990516?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Ayako Oka
Toyoyuki Takada
Hironori Fujisawa
Toshihiko Shiroishi
spellingShingle Ayako Oka
Toyoyuki Takada
Hironori Fujisawa
Toshihiko Shiroishi
Evolutionarily diverged regulation of X-chromosomal genes as a primal event in mouse reproductive isolation.
PLoS Genetics
author_facet Ayako Oka
Toyoyuki Takada
Hironori Fujisawa
Toshihiko Shiroishi
author_sort Ayako Oka
title 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_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_sort evolutionarily diverged regulation of x-chromosomal genes as a primal event in mouse reproductive isolation.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2014-04-01
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.
url http://europepmc.org/articles/PMC3990516?pdf=render
work_keys_str_mv AT ayakooka evolutionarilydivergedregulationofxchromosomalgenesasaprimaleventinmousereproductiveisolation
AT toyoyukitakada evolutionarilydivergedregulationofxchromosomalgenesasaprimaleventinmousereproductiveisolation
AT hironorifujisawa evolutionarilydivergedregulationofxchromosomalgenesasaprimaleventinmousereproductiveisolation
AT toshihikoshiroishi evolutionarilydivergedregulationofxchromosomalgenesasaprimaleventinmousereproductiveisolation
_version_ 1725387868872900608