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导致小鼠雄性不育的易位的减数分裂研究。II. 罗伯逊易位的双杂合子

Meiotic studies of translocations causing male sterility in the mouse. II. Double heterozygotes for Robertsonian translocations.

作者信息

Forejt J

出版信息

Cytogenet Cell Genet. 1979;23(3):163-70. doi: 10.1159/000131322.

Abstract

Unusual meiotic behavior of the XY chromosome pair was observed in sterile male mice doubly heterozygous for two Robertsonian translocations, Rb(16.17)7Bnr and Rb(8.17)1Iem. Nonrandom association between the X chromosome and the translocation configuration, ascertained from the frequencies of relevant C-band contacts, was found in 9 of 10 sterile males. Besides the nonrandom association, the XY chromosomes showed signs of impaired condensation, as judged by measurement of their lengths at diakinesis/MI of the first meiotic division. In contrast, neither nonrandom contact nor decondensation of the XY chromosomes pair was found in fertile males heterozygous for a single Robertsonian translocation, Rb1Iem or Rb7Bnr. The present observations lend indirect support to the working hypothesis advanced previously, the assumption that interference with X-chromosome inactivation is a possible cause of spermatogenic breakdown in carriers of various male-sterile chromosomal transloations. Alternative explanations of the available data, which cannot be ruled out, are briefly discussed.

摘要

在对两种罗伯逊易位Rb(16.17)7Bnr和Rb(8.17)1Iem呈双重杂合状态的不育雄性小鼠中,观察到XY染色体对的异常减数分裂行为。从相关C带接触频率确定,在10只不育雄性小鼠中有9只发现X染色体与易位构型之间存在非随机关联。除了非随机关联外,通过在第一次减数分裂的终变期/中期I测量XY染色体的长度判断,XY染色体还显示出凝缩受损的迹象。相比之下,在对单个罗伯逊易位Rb1Iem或Rb7Bnr呈杂合状态的可育雄性小鼠中,未发现XY染色体对的非随机接触或解凝缩现象。目前的观察结果为先前提出的工作假说提供了间接支持,该假说是认为干扰X染色体失活可能是各种雄性不育染色体易位携带者精子发生障碍的一个原因。文中简要讨论了现有数据的其他无法排除的解释。

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