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本文引用的文献

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LABORATORY EVOLUTION OF POSTPONED SENESCENCE IN DROSOPHILA MELANOGASTER.黑腹果蝇延缓衰老的实验室进化
Evolution. 1984 Sep;38(5):1004-1010. doi: 10.1111/j.1558-5646.1984.tb00370.x.
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Stem cell aging in the Drosophila ovary.果蝇卵巢中的干细胞衰老
Age (Dordr). 2005 Sep;27(3):201-12. doi: 10.1007/s11357-005-2914-1. Epub 2005 Dec 31.
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Insulin/IGF-like signalling, the central nervous system and aging.胰岛素/胰岛素样生长因子信号通路、中枢神经系统与衰老
Biochem J. 2009 Feb 15;418(1):1-12. doi: 10.1042/BJ20082102.
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Insulin levels control female germline stem cell maintenance via the niche in Drosophila.胰岛素水平通过果蝇中的微环境控制雌性生殖系干细胞的维持。
Proc Natl Acad Sci U S A. 2009 Jan 27;106(4):1117-21. doi: 10.1073/pnas.0809144106. Epub 2009 Jan 9.
5
Adult-specific over-expression of the Drosophila genes magu and hebe increases life span and modulates late-age female fecundity.果蝇基因magu和hebe在成年果蝇中的特异性过表达可延长寿命并调节老龄雌性果蝇的繁殖力。
Mol Genet Genomics. 2009 Feb;281(2):147-62. doi: 10.1007/s00438-008-0400-z. Epub 2008 Nov 15.
6
Centrosome misorientation reduces stem cell division during ageing.中心体方向错误会减少衰老过程中的干细胞分裂。
Nature. 2008 Dec 4;456(7222):599-604. doi: 10.1038/nature07386. Epub 2008 Oct 15.
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Drosophila germ-line modulation of insulin signaling and lifespan.果蝇生殖系对胰岛素信号传导及寿命的调节
Proc Natl Acad Sci U S A. 2008 Apr 29;105(17):6368-73. doi: 10.1073/pnas.0709128105. Epub 2008 Apr 23.
8
Imp-L2, a putative homolog of vertebrate IGF-binding protein 7, counteracts insulin signaling in Drosophila and is essential for starvation resistance.Imp-L2是脊椎动物胰岛素样生长因子结合蛋白7的假定同源物,可抵消果蝇中的胰岛素信号传导,并且对饥饿抗性至关重要。
J Biol. 2008;7(3):10. doi: 10.1186/jbiol72. Epub 2008 Apr 15.
9
Caenorhabditis elegans nuclear receptors: insights into life traits.秀丽隐杆线虫核受体:对生命特征的洞察
Trends Endocrinol Metab. 2008 Jul;19(5):153-60. doi: 10.1016/j.tem.2008.02.005. Epub 2008 Apr 10.
10
Drosophila ALS regulates growth and metabolism through functional interaction with insulin-like peptides.果蝇肌萎缩侧索硬化症通过与胰岛素样肽的功能相互作用来调节生长和代谢。
Cell Metab. 2008 Apr;7(4):333-8. doi: 10.1016/j.cmet.2008.02.003.

无脊椎动物遗传模型中的生殖衰老。

Reproductive aging in invertebrate genetic models.

机构信息

Department of Ecology and Evolutionary Biology, Brown University, Providence, Rhode Island 02912, USA.

出版信息

Ann N Y Acad Sci. 2010 Aug;1204:149-55. doi: 10.1111/j.1749-6632.2010.05522.x.

DOI:10.1111/j.1749-6632.2010.05522.x
PMID:20738285
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3125018/
Abstract

The invertebrate genetic systems of Caenorhabditis elegans and Drosophila melanogaster are emerging models to understand the underlying mechanisms of reproductive aging and the relationship between reproduction and lifespan. Both animals show progressive decline in egg production beginning at early middle age, caused in part by reduction in germline stem cell proliferation as well as in survival of developing eggs. Molecular genetic analysis reveals that insulin and TGF-beta signaling are regulators of germline stem cell maintenance and proliferation during aging. Furthermore, the lifespan of both C. elegans and D. melanogaster appears to be regulated by signaling that depends on the presence of germline stem cells in the adult gonad. These invertebrate models provide powerful tools to dissect conserved causes of reproductive aging.

摘要

秀丽隐杆线虫和黑腹果蝇的无脊椎动物遗传系统正在成为理解生殖衰老的潜在机制以及生殖与寿命之间关系的模型。这两种动物的产卵能力都从中年早期开始逐渐下降,部分原因是生殖干细胞增殖减少以及发育中的卵子存活率降低。分子遗传学分析表明,胰岛素和 TGF-β信号是生殖干细胞在衰老过程中维持和增殖的调节因子。此外,秀丽隐杆线虫和黑腹果蝇的寿命似乎都受到依赖于成年性腺中生殖干细胞存在的信号的调节。这些无脊椎动物模型为剖析生殖衰老的保守原因提供了有力的工具。