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XB-ART-475
RNA June 1, 2006; 12 (6): 1084-91.

CUG-BP binds to RNA substrates and recruits PARN deadenylase.

Moraes KC , Wilusz CJ , Wilusz J .


Abstract
CUG-BP is the human homolog of the Xenopus EDEN-BP, which was shown previously to bind to mRNAs, such as c-mos, that exhibit rapid deadenylation following fertilization of the oocyte. While several studies have focused on roles of CUG-BP as a splicing or translation regulator in mammalian cells, its role in mRNA decay has not been examined in detail. Here, we have used an in vitro deadenylation assay to dissect the function of CUG-BP in the decay of two ARE-containing mRNAs: c-fos and TNFalpha. CUG-BP binds specifically to both of these RNAs and stimulates poly(A) shortening by PARN. Moreover, CUG-BP interacts with PARN in extracts by coimmunoprecipitation, and this interaction can be recapitulated using recombinant proteins. CUG-BP, therefore, is the first RNA-binding protein shown to directly recruit a deadenylase to an RNA substrate.

PubMed ID: 16601207
PMC ID: PMC1464848
Article link: RNA
Grant support: [+]

Species referenced: Xenopus
Genes referenced: celf1 fos mos parn

References [+] :
Audic, Embryo deadenylation element-dependent deadenylation is enhanced by a cis element containing AUU repeats. 1998, Pubmed, Xenbase