Suppr超能文献

小鼠gcd2突变导致原始生殖细胞耗竭。

The mouse gcd2 mutation causes primordial germ cell depletion.

作者信息

Reinholdt Laura G, Munroe Robert J, Kamdar Sonja, Schimenti John C

机构信息

The Jackson Laboratory, Bar Harbor, ME 04609, USA.

出版信息

Mech Dev. 2006 Jul;123(7):559-69. doi: 10.1016/j.mod.2006.05.003. Epub 2006 May 25.

Abstract

Germ cell depletion 2 (gcd2) is a chemically induced recessive mutation that causes infertility in male and female mice. The infertility is caused by germ cell depletion as early as 11.5 days post-coitum, when primordial germ cells have completed their migration to the embryonic gonads. Thus, the gcd2 mutation affects the proliferation and/or survival of germ cells after they arrive in the embryonic gonad, a developmental time when little is known about the requirements for germ cell proliferation and survival. The sterility phenotype is incompletely penetrant, has variable expressivity, and is modulated by strain background. The penetrance ranges from 37% in strain C57BL/6J to nearly 100% in CAST/EiJ. Genetic mapping localized gcd2 to a approximately 1Mb region on Chr 2. This interval contains a small number of annotated genes, of which none are known to have a role in germ cell development. Sequencing the coding regions of these genes failed to reveal a mutation, and BACs containing two of the candidate genes failed to rescue the phenotype. This raises the possibilities that the gcd2 mutation resides in non-coding sequences, and regulates genes outside the genetically defined critical region.

摘要

生殖细胞耗竭2(gcd2)是一种化学诱导的隐性突变,可导致雄性和雌性小鼠不育。早在交配后11.5天,当原始生殖细胞完成向胚胎性腺的迁移时,不育就由生殖细胞耗竭引起。因此,gcd2突变影响生殖细胞到达胚胎性腺后的增殖和/或存活,而在这个发育阶段,人们对生殖细胞增殖和存活的需求知之甚少。不育表型不完全外显,具有可变的表达度,并受品系背景的调节。外显率从C57BL/6J品系中的37%到CAST/EiJ品系中的近100%不等。基因定位将gcd2定位到2号染色体上大约1Mb的区域。这个区间包含少量注释基因,其中没有一个已知在生殖细胞发育中起作用。对这些基因的编码区进行测序未能揭示突变,包含两个候选基因的细菌人工染色体也未能挽救该表型。这增加了gcd2突变存在于非编码序列中并调控基因定义关键区域之外的基因的可能性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验