4.7 Article

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

Journal

GENES & DEVELOPMENT
Volume 23, Issue 9, Pages 1046-1051

Publisher

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/gad.1777709

Keywords

microRNAs; miR-24a; apoptosis; caspase9; apaf1

Funding

  1. NIH [GM 42341]

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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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