The mouse X chromosome is enriched for sex-biased genes not subject to selection by meiotic sex chromosome inactivation

Sex chromosomes are subject to sex-specific selective evolutionary forces 1 , 2 . One model predicts that genes with sex-biased expression should be enriched on the X chromosome 2 , 3 , 4 , 5 . In agreement with Rice's hypothesis 3 , spermatogonial genes are over-represented on the X chromosome...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Nature genetics Ročník 36; číslo 6; s. 642 - 646
Hlavní autoři: Khil, Pavel P, Smirnova, Natalya A, Romanienko, Peter J, Camerini-Otero, R Daniel
Médium: Journal Article
Jazyk:angličtina
Vydáno: New York Nature Publishing Group US 01.06.2004
Nature Publishing Group
Témata:
ISSN:1061-4036, 1546-1718
On-line přístup:Získat plný text
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
Popis
Shrnutí:Sex chromosomes are subject to sex-specific selective evolutionary forces 1 , 2 . One model predicts that genes with sex-biased expression should be enriched on the X chromosome 2 , 3 , 4 , 5 . In agreement with Rice's hypothesis 3 , spermatogonial genes are over-represented on the X chromosome of mice 6 and sex- and reproduction-related genes are over-represented on the human X chromosome 7 , 8 . Male-biased genes are under-represented on the X chromosome in worms and flies 9 , 10 , 11 , however. Here we show that mouse spermatogenesis genes are relatively under-represented on the X chromosome and female-biased genes are enriched on it. We used Spo11 −/− mice blocked in spermatogenesis early in meiosis 12 to evaluate the temporal pattern of gene expression in sperm development. Genes expressed before the Spo11 block are enriched on the X chromosome, whereas those expressed later in spermatogenesis are depleted. Inactivation of the X chromosome in male meiosis may be a universal driving force for X-chromosome demasculinization.
Bibliografie:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ISSN:1061-4036
1546-1718
DOI:10.1038/ng1368