共 34 条
microRNA-24a is required to repress apoptosis in the developing neural retina
被引:95
作者:

Walker, James C.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA

Harland, Richard M.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
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.
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页码:1046 / 1051
页数:6
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