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    Title: The transcriptional repression activity of STAF65γ is facilitated by promoter tethering and nuclear import of class IIa histone deacetylases
    Authors: 謝鳳書;Hsieh, Feng-Shu;陳乃慈;Chen, Nai-Tzu;姚雅莉;Yao, Ya-Li;王詩芸;Wang, Shi-Yun;陳健尉;Jeremy, J.W.Chen;賴建成;Lai, Chien-Chen;楊文明;*, Wen-Ming Yang
    Contributors: 生物科技學系
    Keywords: Histone deacetylases;Lung adenocarcinoma;STAF65γ;Transcriptional regulation;YY1
    Date: 2014-07
    Issue Date: 2014-07-03 15:43:43 (UTC+8)
    Abstract: Aberrant expression levels of transcriptional regulators result in alterations in transcriptional control. STAF65γ is a structural subunit of the GCN5 transcriptional co-activator complex. Reports showed that STAF65γ is highly expressed in several human cancer cells, but the consequences of this aberrant expression pattern remain elusive. Here, we show that the STAF65γ protein is highly expressed in lung adenocarcinoma patients and high levels of STAF65γ correlate with poor prognosis. High levels of STAF65γ cause repression of the c-Myc oncogene through physical association with transcription factor YY1 and co-repressors HDACs. Physical interactions between STAF65γ and class IIa HDACs facilitate nuclear enrichment and regulate the assembly of HDAC complexes. Moreover, SUMOylation of STAF65γ is necessary for maintaining the co-repressor complex containing YY1 and class IIa HDACs at the promoter. Our findings reveal a distinct role of STAF65γ in nuclear import, transcriptional repression, and cell cycle regulation at high levels of expression, which is associated with poor clinical outcomes of lung adenocarcinoma.
    Copyright © 2014 Elsevier B.V. All rights reserved.
    Relation: Biochimica et Biophysica Acta-Gene Regulatory Mechanisms, 1839(7):579-91
    Appears in Collections:[Department of Biotechnology] Journal Article

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