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Deletion of human tarbp2 reveals cellular microRNA targets and cell-cycle function of TRBP

Cited 59 time in Web of Science Cited 58 time in Scopus
Authors
Kim, Yoosik; Yeo, Jinah; Lee, Jung Hyun; Cho, Jun; Seo, Daekwan; Kim, Jong-Seo; Kim, V. Narry
Issue Date
2014-11
Citation
Cell Reports, Vol.9 No.3, pp.1061-1074
Abstract
TRBP functions as both a Dicer cofactor and a PKR inhibitor. However, the role of TRBP in microRNA (miRNA) biogenesis is controversial and its regulation of PKR in mitosis remains unexplored. Here, we generate TRBP knockout cells and find altered Dicer-processing sites in a subset of miRNAs but no effect on Dicer stability, miRNA abundance, or Argonaute loading. By generating PACT, another Dicer interactor, and TRBP/PACT double knockout (KO) cells, we further show that TRBP and PACT do not functionally compensate for one another and that only TRBP contributes to Dicer processing. We also report that TRBP is hyperphosphorylated by JNK in M phase when PKR is activated by cellular double-stranded RNAs (dsRNAs). Hyperphosphorylation potentiates the inhibitory activity of TRBP on PKR, suppressing PKR in M-G1 transition. By generating human TRBP KO cells, our study clarifies the role of TRBP and unveils negative feedback regulation of PKR through TRBP phosphorylation.
ISSN
2211-1247
URI
https://hdl.handle.net/10371/171870
DOI
https://doi.org/10.1016/j.celrep.2014.09.039
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College of Natural Sciences (자연과학대학)Dept. of Biological Sciences (생명과학부)Journal Papers (저널논문_생명과학부)
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