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Transcriptional regulation of the cytosolic chaperonin θ subunit gene, Cctq, by Ets domain transcription factors Elk-1, Sap-1a, and net in the absence of serum response factor
被引:18
作者:
Yamazaki, Y
Kubota, H
Nozaki, M
Nagata, K
机构:
[1] Kyoto Univ, Dept Mol & Cellular Biol, Sakyo Ku, Kyoto 6068397, Japan
[2] Kyoto Univ, CREST JST, Inst Frontier Med Sci, Sakyo Ku, Kyoto 6068397, Japan
[3] Osaka Univ, Res Inst Microbial Dis, Dept Sci Lab Anim Expt, Osaka 565, Japan
关键词:
D O I:
10.1074/jbc.M212242200
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The chaperonin-containing t-complex polypeptide 1 (CCT) is a molecular chaperone that facilitates protein folding in eukaryotic cytosol, and the expression of CCT is highly dependent on cell growth. We show here that transcription of the gene encoding the theta subunit of mouse CCT, Cctq, is regulated by the ternary complex factors (TCFs), Elk-1, Sap-1a, and Net (Sap-2). Reporter gene assay using HeLa cells indicated that the Cctq gene promoter contains a cis-acting element of the CCG-GAAGT sequence (CQE1) at -36 bp. The major CQE1-binding proteins in HeLa cell nuclear extract was recognized by anti-Elk-1 or anti-Sap-1a antibodies in electrophoretic mobility shift assay, and recombinant Elk-1, Sap-1a, or Net specifically recognized CQE1. The CQE1-dependent transcriptional activity in HeLa cells was virtually abolished by overexpression of the DNA binding domains of TCFs. Overexpression of full-length TCFs with Ras indicated that exogenous TCFs can regulate the CQE1-dependent transcription in a Ras-dependent manner. PD98059, an inhibitor of MAPK, significantly repressed the CQE1-dependent transcription. However, no serum response factor was detected by electrophoretic mobility shift assay using the CQE1 element. These results indicate that transcription of the Cctq gene is regulated by TCFs under the control of the Ras/MAPK pathway, probably independently of serum response factor.
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页码:30642 / 30651
页数:10
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