The let-7-Imp axis regulates ageing of the Drosophila testis stem-cell niche

被引:131
作者
Toledano, Hila [1 ]
D'Alterio, Cecilia [1 ]
Czech, Benjamin [2 ]
Levine, Erel [3 ,4 ]
Jones, D. Leanne [1 ]
机构
[1] Salk Inst Biol Studies, Genet Lab, La Jolla, CA 92037 USA
[2] Cold Spring Harbor Lab, Howard Hughes Med Inst, Watson Sch Biol Sci, Cold Spring Harbor, NY 11724 USA
[3] Harvard Univ, Dept Phys, Cambridge, MA 02138 USA
[4] Harvard Univ, FAS Ctr Syst Biol, Cambridge, MA 02138 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
RNA-BINDING PROTEIN; MESSENGER-RNA; SELF-RENEWAL; MICRORNA; DIFFERENTIATION; EXPRESSION; IDENTIFICATION; CONTRIBUTES; LIBRARY; REGION;
D O I
10.1038/nature11061
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Adult stem cells support tissue homeostasis and repair throughout the life of an individual. During ageing, numerous intrinsic and extrinsic changes occur that result in altered stem-cell behaviour and reduced tissue maintenance and regeneration. In the Drosophila testis, ageing results in a marked decrease in the self-renewal factor Unpaired (Upd), leading to a concomitant loss of germline stem cells. Here we demonstrate that IGF-II messenger RNA binding protein (Imp) counteracts endogenous small interfering RNAs to stabilize upd (also known as os) RNA. However, similar to upd, Imp expression decreases in the hub cells of older males, which is due to the targeting of Imp by the heterochronic microRNA let-7. In the absence of Imp, upd mRNA therefore becomes unprotected and susceptible to degradation. Understanding the mechanistic basis for ageing-related changes in stem-cell behaviour will lead to the development of strategies to treat age-onset diseases and facilitate stem-cell-based therapies in older individuals.
引用
收藏
页码:605 / +
页数:8
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