Aneuploidy causes premature differentiation of neural and intestinal stem cells

被引:61
|
作者
Gogendeau, Delphine [1 ]
Siudeja, Katarzyna [2 ]
Gambarotto, Davide [1 ]
Pennetier, Carole [1 ]
Bardin, Allison J. [2 ]
Basto, Renata [1 ]
机构
[1] PSL Res Univ, Inst Curie, CNRS, UMR144, F-75005 Paris, France
[2] INSERM, Inst Curie, CNRS, UMR3215,U934, F-75005 Paris, France
来源
NATURE COMMUNICATIONS | 2015年 / 6卷
基金
欧洲研究理事会;
关键词
EXTRA CENTROSOMES; SPINDLE CHECKPOINT; SELF-RENEWAL; DROSOPHILA-MELANOGASTER; TUMOR-SUPPRESSOR; PROGENITOR CELLS; DIVISION; PROTEIN; CYCLE; PROLIFERATION;
D O I
10.1038/ncomms9894
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
Aneuploidy is associated with a variety of diseases such as cancer and microcephaly. Although many studies have addressed the consequences of a non-euploid genome in cells, little is known about their overall consequences in tissue and organism development. Here we use two different mutant conditions to address the consequences of aneuploidy during tissue development and homeostasis in Drosophila. We show that aneuploidy causes brain size reduction due to a decrease in the number of proliferative neural stem cells (NSCs), but not through apoptosis. Instead, aneuploid NSCs present an extended G1 phase, which leads to cell cycle exit and premature differentiation. Moreover, we show that this response to aneuploidy is also present in adult intestinal stem cells but not in the wing disc. Our work highlights a neural and intestine stem cell-specific response to aneuploidy, which prevents their proliferation and expansion.
引用
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页数:15
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