microRNA-24a is required to repress apoptosis in the developing neural retina

被引:95
作者
Walker, James C.
Harland, Richard M. [1 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
关键词
microRNAs; miR-24a; apoptosis; caspase9; apaf1; CELL-DEATH; GANGLION-CELLS; INVOLVEMENT; EXPRESSION; SURVIVAL; DIFFERENTIATION; PATTERNS; MIRNAS; GROWTH;
D O I
10.1101/gad.1777709
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Programmed cell death is important for the proper development of the retina, and microRNAs (miRNAs) may be critical for its regulation. Here, we report that miR-24a is expressed in the neural retina and is required for correct eye morphogenesis in Xenopus. Inhibition of miR-24a during development causes a reduction in eye size due to a significant increase in apoptosis in the retina, whereas overexpression of miR-24a is sufficient to prevent apoptosis. We show that miR-24a negatively regulates the proapoptotic factors caspase9 and apaf1, demonstrating a role for miRNAs in the regulation of apoptosis during normal development.
引用
收藏
页码:1046 / 1051
页数:6
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