11 Regulation of mRNA Molecules by MicroRNAs
Abstract
HISTORICAL BACKGROUND ON ANIMAL miRNAs
lin-4 was identified as a loss-of-function mutation that gave rise to re-iterations in cell lineages, retarded development, and abnormal morphology in C. elegans (Horvitz and Sulston 1980; Chalfie et al. 1981). Additional genetic screens identified semidominant gain-of-function mutations in the lin-14 gene that, like the lin-4 mutation, led to cell lineage reiteration and retarded development (Ambros and Horvitz 1984Ambros and Horvitz 1987). On the basis of the similar phenotypes of the lin-4 loss-of-function and lin-14 gain-of-function mutants, it was postulated that the two genes interact genetically (Ambros 1989). Indeed, epistasis experiments revealed that the lin-4 mutant phenotype was dependent on lin-14, suggesting that the role of the lin-4 gene product is to act as a negative regulator of lin-14 (Ambros 1989).
The mechanism by which lin-4 negatively regulates lin-14 was unknown until 1991, when it was demonstrated that the lin-4 gene product down-regulated lin-14 protein levels by interacting with the lin-14 3′ untranslated region (3′UTR) (Arasu et al. 1991; Wightman et al. 1991). Subsequently, the lin-4 gene product was discovered to be...
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PDFDOI: http://dx.doi.org/10.1101/0.297-318