Literature DB >> 11173831

A high frequency of XO offspring from X(Paf)Y* male mice: evidence that the Paf mutation involves an inversion spanning the X PAR boundary.

P S Burgoyne1, E P Evans.   

Abstract

It has previously been reported that 19% of the daughters of males carrying the X-linked mutation patchy fur (Paf) are XO with a maternally derived X chromosome. We now report that hemizygous Paf males that also carry the variant Y chromosome Y*, show a much increased XO production ( approximately 40% of daughters). We hypothesize that the Paf mutation is associated with an inversion spanning the pseudoautosomal region (PAR) boundary, and that this leads to preferential crossing over between the resulting inverted region of PAR and an equivalent inverted PAR region within the compound Y* PAR. This would lead to the production of dicentric X and acentric Y products and consequent sex chromosome loss. This interpretation is supported by analysis of the sex chromosome complements at the second meiotic metaphase, which revealed a high incidence of dicentrics. Another curious feature of the Paf mutation is that mice that are homozygous Paf have more hair than mice that are hemizygous Paf. This can be explained if the Paf mutation is a hypomorphic mutation that escapes X inactivation because, unlike the wild type allele, it is now located within the PAR. Copyright 2001 S. Karger AG, Basel

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Year:  2000        PMID: 11173831     DOI: 10.1159/000056819

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  19 in total

1.  Sex-specific differences in meiotic chromosome segregation revealed by dicentric bridge resolution in mice.

Authors:  Kara E Koehler; Elise A Millie; Jonathan P Cherry; Paul S Burgoyne; Edward P Evans; Patricia A Hunt; Terry J Hassold
Journal:  Genetics       Date:  2002-11       Impact factor: 4.562

Review 2.  Mouse model systems to study sex chromosome genes and behavior: relevance to humans.

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4.  Premature ovarian insufficiency in the XO female mouse on the C57BL/6J genetic background.

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7.  The presence of the Y-chromosome, not the absence of the second X-chromosome, alters the mRNA levels stored in the fully grown XY mouse oocyte.

Authors:  Baozeng Xu; Yayoi Obata; Feng Cao; Teruko Taketo
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8.  Wnt pathway anomalies in developing amygdalae of Turner syndrome-like mice.

Authors:  Adam S Raefski; Benjamin R Carone; Anupinder Kaur; Winfried Krueger; Michael J O'Neill
Journal:  J Mol Neurosci       Date:  2007       Impact factor: 2.866

9.  The expression of Y-linked Zfy2 in XY mouse oocytes leads to frequent meiosis 2 defects, a high incidence of subsequent early cleavage stage arrest and infertility.

Authors:  Nadège Vernet; Maria Szot; Shantha K Mahadevaiah; Peter J I Ellis; Fanny Decarpentrie; Obah A Ojarikre; Áine Rattigan; Teruko Taketo; Paul S Burgoyne
Journal:  Development       Date:  2014-02       Impact factor: 6.868

10.  Mouse Y-linked Zfy1 and Zfy2 are expressed during the male-specific interphase between meiosis I and meiosis II and promote the 2nd meiotic division.

Authors:  Nadège Vernet; Shantha K Mahadevaiah; Yasuhiro Yamauchi; Fanny Decarpentrie; Michael J Mitchell; Monika A Ward; Paul S Burgoyne
Journal:  PLoS Genet       Date:  2014-06-26       Impact factor: 5.917

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