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小鼠mei8的定位克隆与特征分析,mei8是减数分裂黏连蛋白Rec8的一个破坏等位基因。

Positional cloning and characterization of mouse mei8, a disrupted allelle of the meiotic cohesin Rec8.

作者信息

Bannister Laura A, Reinholdt Laura G, Munroe Robert J, Schimenti John C

机构信息

The Jackson Laboratory, Bar Harbor, Maine, USA.

出版信息

Genesis. 2004 Nov;40(3):184-94. doi: 10.1002/gene.20085.

Abstract

A novel mutation, mei8, was isolated in a forward genetic screen for infertility mutations induced by chemical mutagenesis of ES cells. Homozygous mutant mice are sterile. Mutant females exhibit ovarian dysgenesis and lack ovarian follicles at reproductive maturity. Affected males have small testes due to arrest of spermatogenesis during meiotic prophase I. Genetic mapping and positional cloning of mei8 led to the identification of a mutation in Rec8, a homolog of the yeast meiosis-specific cohesin gene REC8. Analysis of meiosis in Rec8(mei8)/Rec8(mei8) spermatocytes showed that, while initiation of recombination and synapsis occurs, REC8 is required for the completion and/or maintenance of synapsis, cohesion of sister chromatids, and the formation of chiasmata, as it is in other organisms. However, unlike yeast and Caenorhabditis elegans, localization of REC8 on meiotic chromosomes is not required for the assembly of axial elements.

摘要

在一项针对通过化学诱变ES细胞诱导不育突变的正向遗传筛选中,分离出一种新的突变体mei8。纯合突变小鼠不育。突变雌性小鼠表现出卵巢发育不全,在生殖成熟时缺乏卵巢卵泡。受影响的雄性小鼠由于减数分裂前期I期间精子发生停滞而睾丸较小。对mei8进行遗传定位和位置克隆后,发现Rec8发生了突变,Rec8是酵母减数分裂特异性黏连蛋白基因REC8的同源物。对Rec8(mei8)/Rec8(mei8)精母细胞减数分裂的分析表明,虽然重组和联会起始发生,但正如在其他生物体中一样,REC8对于联会的完成和/或维持、姐妹染色单体的黏连以及交叉的形成是必需的。然而,与酵母和秀丽隐杆线虫不同,轴向元件的组装不需要REC8定位在减数分裂染色体上。

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