Female meiotic sex chromosome inactivation in chicken.

During meiotic prophase in male mammals, the heterologous X and Y chromosomes remain largely unsynapsed, and meiotic sex chromosome inactivation (MSCI) leads to formation of the transcriptionally silenced XY body. In birds, the heterogametic sex is female, carrying Z and W chromosomes (ZW), whereas...

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Main Authors: Sam Schoenmakers, Evelyne Wassenaar, Jos W Hoogerbrugge, Joop S E Laven, J Anton Grootegoed, Willy M Baarends
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-05-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC2678266?pdf=render
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author Sam Schoenmakers
Evelyne Wassenaar
Jos W Hoogerbrugge
Joop S E Laven
J Anton Grootegoed
Willy M Baarends
author_facet Sam Schoenmakers
Evelyne Wassenaar
Jos W Hoogerbrugge
Joop S E Laven
J Anton Grootegoed
Willy M Baarends
author_sort Sam Schoenmakers
collection DOAJ
description During meiotic prophase in male mammals, the heterologous X and Y chromosomes remain largely unsynapsed, and meiotic sex chromosome inactivation (MSCI) leads to formation of the transcriptionally silenced XY body. In birds, the heterogametic sex is female, carrying Z and W chromosomes (ZW), whereas males have the homogametic ZZ constitution. During chicken oogenesis, the heterologous ZW pair reaches a state of complete heterologous synapsis, and this might enable maintenance of transcription of Z- and W chromosomal genes during meiotic prophase. Herein, we show that the ZW pair is transiently silenced, from early pachytene to early diplotene using immunocytochemistry and gene expression analyses. We propose that ZW inactivation is most likely achieved via spreading of heterochromatin from the W on the Z chromosome. Also, persistent meiotic DNA double-strand breaks (DSBs) may contribute to silencing of Z. Surprisingly, gammaH2AX, a marker of DSBs, and also the earliest histone modification that is associated with XY body formation in mammalian and marsupial spermatocytes, does not cover the ZW during the synapsed stage. However, when the ZW pair starts to desynapse, a second wave of gammaH2AX accumulates on the unsynapsed regions of Z, which also show a reappearance of the DSB repair protein RAD51. This indicates that repair of meiotic DSBs on the heterologous part of Z is postponed until late pachytene/diplotene, possibly to avoid recombination with regions on the heterologously synapsed W chromosome. Two days after entering diplotene, the Z looses gammaH2AX and shows reactivation. This is the first report of meiotic sex chromosome inactivation in a species with female heterogamety, providing evidence that this mechanism is not specific to spermatogenesis. It also indicates the presence of an evolutionary force that drives meiotic sex chromosome inactivation independent of the final achievement of synapsis.
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spelling doaj.art-032f8631883c433f8091d66823b2e37b2022-12-22T00:52:53ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042009-05-0155e100046610.1371/journal.pgen.1000466Female meiotic sex chromosome inactivation in chicken.Sam SchoenmakersEvelyne WassenaarJos W HoogerbruggeJoop S E LavenJ Anton GrootegoedWilly M BaarendsDuring meiotic prophase in male mammals, the heterologous X and Y chromosomes remain largely unsynapsed, and meiotic sex chromosome inactivation (MSCI) leads to formation of the transcriptionally silenced XY body. In birds, the heterogametic sex is female, carrying Z and W chromosomes (ZW), whereas males have the homogametic ZZ constitution. During chicken oogenesis, the heterologous ZW pair reaches a state of complete heterologous synapsis, and this might enable maintenance of transcription of Z- and W chromosomal genes during meiotic prophase. Herein, we show that the ZW pair is transiently silenced, from early pachytene to early diplotene using immunocytochemistry and gene expression analyses. We propose that ZW inactivation is most likely achieved via spreading of heterochromatin from the W on the Z chromosome. Also, persistent meiotic DNA double-strand breaks (DSBs) may contribute to silencing of Z. Surprisingly, gammaH2AX, a marker of DSBs, and also the earliest histone modification that is associated with XY body formation in mammalian and marsupial spermatocytes, does not cover the ZW during the synapsed stage. However, when the ZW pair starts to desynapse, a second wave of gammaH2AX accumulates on the unsynapsed regions of Z, which also show a reappearance of the DSB repair protein RAD51. This indicates that repair of meiotic DSBs on the heterologous part of Z is postponed until late pachytene/diplotene, possibly to avoid recombination with regions on the heterologously synapsed W chromosome. Two days after entering diplotene, the Z looses gammaH2AX and shows reactivation. This is the first report of meiotic sex chromosome inactivation in a species with female heterogamety, providing evidence that this mechanism is not specific to spermatogenesis. It also indicates the presence of an evolutionary force that drives meiotic sex chromosome inactivation independent of the final achievement of synapsis.http://europepmc.org/articles/PMC2678266?pdf=render
spellingShingle Sam Schoenmakers
Evelyne Wassenaar
Jos W Hoogerbrugge
Joop S E Laven
J Anton Grootegoed
Willy M Baarends
Female meiotic sex chromosome inactivation in chicken.
PLoS Genetics
title Female meiotic sex chromosome inactivation in chicken.
title_full Female meiotic sex chromosome inactivation in chicken.
title_fullStr Female meiotic sex chromosome inactivation in chicken.
title_full_unstemmed Female meiotic sex chromosome inactivation in chicken.
title_short Female meiotic sex chromosome inactivation in chicken.
title_sort female meiotic sex chromosome inactivation in chicken
url http://europepmc.org/articles/PMC2678266?pdf=render
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