English  |  正體中文  |  简体中文  |  Items with full text/Total items : 69561/69561 (100%)
Visitors : 23133840      Online Users : 792
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version


    Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/27759


    Title: P/CAF rescues the Bhlhe40-mediated repression of MyoD transactivation
    Authors: Hsiao,SP;Huang,KM;Chang,HY;Chen,SL
    Contributors: 生命科學研究所
    Keywords: HELIX-LOOP-HELIX;COACTIVATOR 1-ALPHA PGC-1-ALPHA;BOX TRANSCRIPTION FACTORS;CELL DIFFERENTIATION;SKELETAL-MUSCLE;RECEPTOR-ALPHA;DEC1 STRA13;EXPRESSION;PGC-1;ACTIVATION
    Date: 2009
    Issue Date: 2010-06-29 19:28:58 (UTC+8)
    Publisher: 中央大學
    Abstract: Previously, we found that MRFs (myogenic regulatory factors) regulated the expression of PGC-1 alpha (peroxisome-proliferator-activated receptor gamma co-activator 1 alpha) by targeting a short region, from nt -49 to +2 adjacent to the transcription initiation site, that contained two E-boxes. However, only the E2-box had significant affinity for MRFs, and the E1-box was predicted to be the target of Bhlhe40 (basic helix-loop-helix family, member e40, also known as Stra13, Bhlhb2, DEC1 and Sharp2), a transcriptional repressor implicated in the regulation of several physiological processes. In the present study, by using EMSA (electrophoresis mobility-shift assay), we confirmed that Bhlhe40 targeted the El-box and formed a complex with the basic helix-loop-helix transcription factor MyoD (myogenic differentiation factor D) on the PGC-1 alpha core promoter. We demonstrate that Bhlhe40 binds to the promoters of PGC-1 alpha and myogenic genes in vivo and that Bhlhe40 represses the MyoD-mediated transactivation of these promoters. Furthermore, we found that this repression could be relieved by P/CAF (p300/CBP-associated factor) in a dose-dependent manner, but not by CBP [CREB (cAMP-response-element-binding protein)-binding protein]. Bhlhe40 interacted with P/CAF and this interaction disrupted the interaction between P/CAF and MyoD. These results suggest that Bhlhe40 functions as a repressor of MyoD by binding to adjacent E-boxes and sequestering P/CAF from MyoD.
    Relation: BIOCHEMICAL JOURNAL
    Appears in Collections:[生命科學研究所 ] 期刊論文

    Files in This Item:

    File Description SizeFormat
    index.html0KbHTML731View/Open


    All items in NCUIR are protected by copyright, with all rights reserved.

    社群 sharing

    ::: Copyright National Central University. | 國立中央大學圖書館版權所有 | 收藏本站 | 設為首頁 | 最佳瀏覽畫面: 1024*768 | 建站日期:8-24-2009 :::
    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback  - 隱私權政策聲明