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PMID: 18377426 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Interaction of antiproliferative protein Tob with the CCR4-NOT deadenylase complex.

Cancer science ·Vol. 99 ·No. 4 ·2008-04-00 ·Pages 755-61

Miyasaka T, Morita M, Ito K, Suzuki T, Fukuda H, Takeda S, Inoue J, Semba K, Yamamoto T

Abstract

Tob protein, when overexpressed, suppresses growth of NIH3T3 cells, presumably by regulating expression of various growth-related genes. However, the molecular mechanisms underlying Tob-mediated regulation of gene expression have been obscure. To address this issue we established stable Tob-expressing cell lines and used a proteomics approach to identify Tob-interacting proteins. We found that Tob associates with the CCR4-NOT complex. The carboxyl-terminal half of Tob interacted with Cnot1, a core protein of the CCR4-NOT complex. We further showed that the deadenylase activity associated with the complex was suppressed in vitro by Tob. These results suggest that the antiproliferative activity of Tob is shown post-transcriptionally by controlling the stability of the target mRNAs in addition to its involvement in transcriptional regulation, reported previously.

MeSH Terms
Animals Cell Proliferation HeLa Cells Humans Intracellular Signaling Peptides and Proteins/genetics,metabolism Mice NIH 3T3 Cells Protein Biosynthesis/genetics Proteomics RNA Stability Ribonucleases/metabolism Transcription Factors/metabolism Tumor Suppressor Proteins/genetics,metabolism
Chemicals
CNOT1 protein, human Intracellular Signaling Peptides and Proteins TOB1 protein, human Transcription Factors Tumor Suppressor Proteins Ribonucleases mRNA deadenylase
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Miyasaka Takashi
Division of Oncology, Institute of Medical Science, University of Tokyo, 4-6-1 Shirokanedai Minato-ku, Tokyo 108-8639, Japan.
Morita Masahiro
Ito Kentaro
Suzuki Toru
Fukuda Hiroyuki
Takeda Shizu
Inoue Jun-Ichiro
Semba Kentaro
Yamamoto Tadashi
Article Info
Journal
Cancer science
Abbr.
Cancer Sci
ISSN
1349-7006
Published
2008-04-00
Pages
755-61
Language
English
Region
England
NLM ID
101168776
Subset
IM
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