The FLYWCH transcription factors FLH-1, FLH-2, and FLH-3 repress embryonic expression of microRNA genes in C. elegans
Authors
Ow, Maria C.Martinez, Natalia Julia
Olsen, Philip H.
Silverman, Howard S.
Barrasa, M. Inmaculada
Conradt, Barbara
Walhout, Albertha J. M.
Ambros, Victor R.
UMass Chan Affiliations
Program in Gene Function and ExpressionProgram in Molecular Medicine
Graduate School of Biomedical Sciences
Document Type
Journal ArticlePublication Date
2008-09-17Keywords
Amino Acid Sequence; Animals; Binding Sites; Caenorhabditis elegans; *Gene Expression Regulation, Developmental; *Genes, Helminth; MicroRNAs; Molecular Sequence Data; RNA Interference; Sequence Homology, Amino Acid; Transcription FactorsLife Sciences
Medicine and Health Sciences
Metadata
Show full item recordAbstract
MicroRNAs (miRNAs) are small noncoding RNAs that regulate gene expression post-transcriptionally via antisense base-pairing. Although miRNAs are involved in a variety of important biological functions, little is known about their transcriptional regulation. Using yeast one-hybrid assays, we identified transcription factors with a FLYWCH Zn-finger DNA-binding domain that bind to the promoters of several Caenorhabditis elegans miRNA genes. The products of the flh-1 and flh-2 genes function redundantly to repress embryonic expression of lin-4, mir-48, and mir-241, miRNA genes that are normally expressed only post-embryonically. Although single mutations in either flh-1 or flh-2 genes result in a viable phenotype, double mutation of flh-1 and flh-2 results in early larval lethality and an enhanced derepression of their target miRNAs in embryos. Double mutations in flh-2 and a third FLYWCH Zn-finger-containing transcription factor, flh-3, also result in enhanced precocious expression of target miRNAs. Mutations of lin-4 or mir-48andmir-241 do not rescue the lethal flh-1; flh-2 double-mutant phenotype, suggesting that the inviability is not solely the result of precocious expression of these miRNAs. Therefore, the FLH-1 and FLH-2 proteins likely play a more general role in regulating gene expression in embryos.Source
Genes Dev. 2008 Sep 15;22(18):2520-34. Link to article on publisher's siteDOI
10.1101/gad.1678808Permanent Link to this Item
http://hdl.handle.net/20.500.14038/32799PubMed ID
18794349; 18794349Related Resources
Link to Article in PubMedae974a485f413a2113503eed53cd6c53
10.1101/gad.1678808
