CRD-BP Protects the Coding Region of βTrCP1 mRNA from miR-183-Mediated Degradation
Ribonuclease III
0301 basic medicine
Binding Sites
Recombinant Fusion Proteins
Eukaryotic Initiation Factor-2
RNA-Binding Proteins
Cell Biology
beta-Transducin Repeat-Containing Proteins
DEAD-box RNA Helicases
MicroRNAs
Open Reading Frames
03 medical and health sciences
Argonaute Proteins
Humans
RNA-Induced Silencing Complex
RNA, Messenger
Molecular Biology
DOI:
10.1016/j.molcel.2009.06.007
Publication Date:
2009-07-31T17:09:07Z
AUTHORS (4)
ABSTRACT
miRNAs are largely known to base pair with the 3'UTR of target mRNAs, downregulating their stability and translation. mRNA of betaTrCP1 ubiquitin ligase is very unstable, but unlike the majority of mRNAs where 3'UTR determines the rate of mRNA turnover, betaTrCP1 mRNA contains cis-acting destabilizing elements within its coding region. Here we show that degradation of mRNA of betaTrCP1 is miRNA dependent and identify miR-183 as a microRNA that interacts with the coding region of betaTrCP1 mRNA. Argonaute2 interacts with the same region of betaTrCP1 mRNA in an miR-183-dependent manner. Inhibition of miR-183 function or disruption of the miR-183-binding site stabilizes betaTrCP1 mRNA and elevates betaTrCP1 levels, resulting in activation of the SCF(betaTrCP) E3 ubiquitin ligase. We previously showed that the RNA-binding protein CRD-BP binds to the coding region of betaTrCP1 mRNA and stabilizes it. Here we demonstrate that CRD-BP prevents degradation of betaTrCP1 mRNA by attenuating its miR-183-dependent interaction with Ago2.
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CITATIONS (173)
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