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Dev Dyn ; 234(4): 1046-54, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16247770

ABSTRACT

In C. elegans, heterochronic genes control the timing of cell fate determination during development. Two heterochronic genes, let-7 and lin-4, encode microRNAs (miRNAs) that down-regulate a third heterochronic gene lin-41 by binding to complementary sites in its 3'UTR. let-7 and lin-4 are conserved in mammals. Here we report the cloning and sequencing of mammalian lin-41 orthologs. We find that mouse and human lin-41 genes contain predicted conserved complementary sites for let-7 and the lin-4 ortholog, mir-125, in their 3'UTRs. Mouse lin-41 (Mlin-41) is temporally expressed in developing mouse embryos, most dramatically in the limb buds. Mlin-41 is down-regulated during mid-embryogenesis at the time when mouse let-7c and mir-125 RNA levels are up-regulated. Our results suggest that mammalian lin-41 is temporally regulated by miRNAs in order to direct key developmental events such as limb formation.


Subject(s)
Embryo, Mammalian/metabolism , Gene Expression Regulation, Developmental , MicroRNAs/metabolism , Transcription Factors/metabolism , Amino Acid Sequence , Animals , Base Pairing , Base Sequence , Binding Sites/genetics , Blotting, Northern , Cloning, Molecular , Conserved Sequence/genetics , DNA Primers , Extremities/embryology , Gene Components , In Situ Hybridization , Mice , Molecular Sequence Data , Sequence Analysis, DNA , Transcription Factors/genetics
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