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Bioessays. 2002 Feb;24(2):119-29.

Control of developmental timing by small temporal RNAs: a paradigm for RNA-mediated regulation of gene expression.

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  • 1Department of Molecular, Cellular and Development Biology, Yale University, 266 Whitney Ave., New Haven, CT 06520, USA.

Abstract

Heterochronic genes control the timing of developmental programs. In C. elegans, two key genes in the heterochronic pathway, lin-4 and let-7, encode small temporally expressed RNAs (stRNAs) that are not translated into protein. These stRNAs exert negative post-transcriptional regulation by binding to complementary sequences in the 3' untranslated regions of their target genes. stRNAs are transcribed as longer precursor RNAs that are processed by the RNase Dicer/DCR-1 and members of the RDE-1/AGO1 family of proteins, which are better known for their roles in RNA interference (RNAi). However, stRNA function appears unrelated to RNAi. Both sequence and temporal regulation of let-7 stRNA is conserved in other animal species suggesting that this is an evolutionarily ancient gene. Indeed, C. elegans, Drosophila and humans encode at least 86 other RNAs with similar structural features to lin-4 and let-7. We postulate that other small non-coding RNAs may function as stRNAs to control temporal identity during development in C. elegans and other organisms.

Copyright 2002 Wiley Periodicals, Inc.

PMID:
11835276
[PubMed - indexed for MEDLINE]
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