Suppr超能文献

[t单倍型的减数分裂驱动:部分三体小鼠染色体的分离]

[Meiotic drive of t-haplotypes: segregation of chromosomes in mice with partial trisomy].

作者信息

Agul'nik A I, Agul'nik S I, Ruvinskiĭ A O

出版信息

Genetika. 1990 Oct;26(10):1776-82.

PMID:2283048
Abstract

The properties of the t haplotypes, specific mutant states of the proximal region of chromosome 17 in the house mouse keep renewing interest. One such property is increased transmission of the t haplotype from heterozygous t/+ males to their offspring. By means of reciprocal translocation T (16; 17)43H, we have constructed males with tertiary trisomy 17 (+T43/++/RB7+) carrying Robertsonian translocation Rb(16.17)7Bnr. The offspring of these males was viable when sperm of +T43/++ and Rb7+ was used. The segregation patterns in the offspring of t-bearing trisomics were analysed on days 16-18 of embryonic development. It was found that in the case when the t haplotype is on the normal acrocentric (male male ++T43/+t12+/Rb7++), its presence in the gamete +t12+/++T43 does not produce meiotic drive. However, when t6 is on Rb7, meiotic drive was equal to 80%. It is concluded that the presence of a normal homolog and a t-bearing chromosome in sperm does not result in meiotic drive. Possible mechanisms of meiotic drive of the t haplotypes are discussed.

摘要

小家鼠17号染色体近端区域的特定突变状态——t单倍型的特性一直引发着人们的兴趣。其中一个特性是t单倍型从杂合子t/+雄性向其后代的传递增加。通过相互易位T(16;17)43H,我们构建了携带罗伯逊易位Rb(16.17)7Bnr的17号染色体三级三体(+T43/++/RB7+)雄性个体。当使用+T43/++和Rb7+的精子时,这些雄性个体的后代是可存活的。在胚胎发育的第16至18天分析了携带t的三体后代的分离模式。结果发现,当t单倍型位于正常近端着丝粒染色体上时(雄性雄性++T43/+t12+/Rb7++),其在配子+t12+/++T43中的存在不会产生减数分裂驱动。然而,当t6位于Rb7上时,减数分裂驱动等于80%。得出的结论是,精子中正常同源染色体和携带t的染色体的存在不会导致减数分裂驱动。文中讨论了t单倍型减数分裂驱动的可能机制。

相似文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验