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2
Cyclin E and Cdk2 control GLD-1, the mitosis/meiosis decision, and germline stem cells in Caenorhabditis elegans.细胞周期蛋白 E 和 CDK2 控制 GLD-1、有丝分裂/减数分裂的决定以及秀丽隐杆线虫中的生殖干细胞。
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本文引用的文献

1
Vitamin A in reproduction and development.维生素 A 在生殖和发育中的作用。
Nutrients. 2011 Apr;3(4):385-428. doi: 10.3390/nu3040385. Epub 2011 Mar 29.
2
C. elegans star proteins, GLD-1 and ASD-2, regulate specific RNA targets to control development.秀丽隐杆线虫的星体蛋白 GLD-1 和 ASD-2 通过调控特定的 RNA 靶标来控制发育。
Adv Exp Med Biol. 2010;693:106-22. doi: 10.1007/978-1-4419-7005-3_8.
3
The C. elegans adult male germline: stem cells and sexual dimorphism.秀丽隐杆线虫雄性生殖系的成年个体:干细胞与性二态性。
Dev Biol. 2010 Oct 15;346(2):204-14. doi: 10.1016/j.ydbio.2010.07.022. Epub 2010 Jul 24.
4
PRP-17 and the pre-mRNA splicing pathway are preferentially required for the proliferation versus meiotic development decision and germline sex determination in Caenorhabditis elegans.PRP-17 和前体 mRNA 剪接途径在秀丽隐杆线虫的增殖与减数分裂发育决策以及生殖细胞性别决定中优先需要。
Dev Dyn. 2010 May;239(5):1555-72. doi: 10.1002/dvdy.22274.
5
Female gametophyte development in flowering plants.开花植物中的雌配子体发育。
Annu Rev Plant Biol. 2010;61:89-108. doi: 10.1146/annurev-arplant-042809-112203.
6
The Nanos3-3'UTR is required for germ cell specific NANOS3 expression in mouse embryos.Nanos3-3'UTR 对于小鼠胚胎中生殖细胞特异性 NANOS3 表达是必需的。
PLoS One. 2010 Feb 18;5(2):e9300. doi: 10.1371/journal.pone.0009300.
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Transgenic solutions for the germline.种系的转基因解决方案。
WormBook. 2010 Feb 8:1-21. doi: 10.1895/wormbook.1.148.1.
8
Genome-wide analysis of mRNA targets for Caenorhabditis elegans FBF, a conserved stem cell regulator.全基因组分析 Caenorhabditis elegans FBF 的 mRNA 靶标,FBF 是一种保守的干细胞调节因子。
Proc Natl Acad Sci U S A. 2010 Feb 23;107(8):3936-41. doi: 10.1073/pnas.1000495107. Epub 2010 Feb 8.
9
Insulin signaling promotes germline proliferation in C. elegans.胰岛素信号促进秀丽隐杆线虫生殖系的增殖。
Development. 2010 Feb;137(4):671-80. doi: 10.1242/dev.042523.
10
Progression from a stem cell-like state to early differentiation in the C. elegans germ line.线虫生殖系中从干细胞样状态到早期分化的进展。
Proc Natl Acad Sci U S A. 2010 Feb 2;107(5):2048-53. doi: 10.1073/pnas.0912704107. Epub 2010 Jan 13.

多细胞生物中细胞有丝分裂/减数分裂决策的分子调控。

Molecular regulation of the mitosis/meiosis decision in multicellular organisms.

机构信息

Howard Hughes Medical Institute, Department of Biochemistry, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.

出版信息

Cold Spring Harb Perspect Biol. 2011 Aug 1;3(8):a002683. doi: 10.1101/cshperspect.a002683.

DOI:10.1101/cshperspect.a002683
PMID:21646377
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3140684/
Abstract

A major step in the journey from germline stem cell to differentiated gamete is the decision to leave the mitotic cell cycle and begin progression through the meiotic cell cycle. Over the past decade, molecular regulators of the mitosis/meiosis decision have been discovered in most of the major model multicellular organisms. Historically, the mitosis/meiosis decision has been closely linked with controls of germline self-renewal and the sperm/egg decision, especially in nematodes and mice. Molecular explanations of those linkages clarify our understanding of this fundamental germ cell decision, and unifying themes have begun to emerge. Although the complete circuitry of the decision is not known in any organism, the recent advances promise to impact key issues in human reproduction and agriculture.

摘要

从生殖细胞到分化配子的旅程中,一个主要步骤是决定离开有丝分裂细胞周期并开始进入减数分裂细胞周期。在过去的十年中,大多数主要的多细胞模式生物中已经发现了有丝分裂/减数分裂决定的分子调节剂。从历史上看,有丝分裂/减数分裂决定与生殖系自我更新和精子/卵子决定密切相关,尤其是在线虫和小鼠中。这些联系的分子解释阐明了我们对这一基本生殖细胞决定的理解,并且开始出现统一的主题。尽管在任何生物体中都不知道该决定的完整电路,但最近的进展有望影响人类生殖和农业的关键问题。