4.7 Article

The let-7 microRNA family members mir-48, mir-84, and mir-241 function together to regulate developmental timing in Caenorhabditis elegans

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DEVELOPMENTAL CELL
卷 9, 期 3, 页码 403-414

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CELL PRESS
DOI: 10.1016/j.devcel.2005.07.009

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  1. NIGMS NIH HHS [GM34028, GM067031, 5F32GM065721-02, F32 GM065721, R01 GM067031, F32 GM065721-03, R01 GM034028] Funding Source: Medline

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The microRNA let-7 is a critical regulator of developmental timing events at the larval-to-adult transition in C. elegans. Recently, microRNAs with sequence similarity to let-7 have been identified. We find that doubly mutant animals lacking the let-7family microRNA genes mir-48 and mir-84 exhibit retarded molting behavior and retarded adult gene expression in the hypodermis. Triply mutant animals lacking mir-48, mir-84, and mir-241 exhibit repetition of L2-stage events in addition to retarded adult-stage events. mir-48, mir-84, and mir-241 function together to control the L2-to-L3 transition, likely by base pairing to complementary sites in the hbi-13 ' UTR and downregulating hbi-1 activity. Genetic analysis indicates that mir-48, mir-84, and mir-241 specify the timing of the L2-to-L3 transition in parallel to the heterochronic genes lin-28 and lin-46. These results indicate that let-7family microRNAs function in combination to affect both early and late developmental timing decisions.

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