Zimp7和Zimp10是两个新的pnas样蛋白,具有雄激素受体共调节因子的功能。

Nuclear receptor signaling Pub Date : 2006-01-01 Epub Date: 2006-07-07 DOI:10.1621/nrs.04017
Jason Beliakoff, Zijie Sun
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引用次数: 32

摘要

雄激素受体(AR)在男性性发育以及正常和恶性前列腺细胞的生长和存活中起着至关重要的作用。研究表明,AR转录激活是通过与多种转录共调节因子的相互作用来调节的。活化STATs的蛋白抑制剂(PIAS)是转录共调节因子,并已被证明可以调节ar介导的转录。本文综述了近年来国内外对两种新的pnas样蛋白Zimp7和Zimp10的研究进展。特别地,我们讨论了AR和这两种蛋白之间的功能相互作用,以及它们调节AR介导的转录的潜在机制。此外,我们利用最近的Zimp10敲除小鼠模型探索了Zimp10在体内转录调控中的潜在作用。综上所述,到目前为止,我们的发现表明Zimp7和Zimp10在功能上是非冗余的,并且具有PIAS家族中未描述的独特特征。进一步研究这两种pias样蛋白的功能作用可能有助于更好地了解前列腺癌的进展,并为治疗干预提供可能的新靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Zimp7 and Zimp10, two novel PIAS-like proteins, function as androgen receptor coregulators.

The androgen receptor (AR) plays a critical role in male sexual development and in normal and malignant prostate cell growth and survival. It has been shown that AR transcriptional activation is regulated through interactions with a variety of transcriptional co-regulators. The Protein Inhibitors of Activated STATs (PIAS) are transcriptional co-regulators, and have been shown to modulate AR-mediated transcription. In this brief, we summarize our recent studies on two novel PIAS-like proteins, Zimp7 and Zimp10. Particularly, we address the functional interactions between the AR and these two proteins, and potential mechanisms by which they regulate AR mediated transcription. In addition, we explore potential roles of Zimp10 in transcriptional regulation in vivo using a recent Zimp10 knockout mouse model. Taken together, our findings thus far suggest that Zimp7 and Zimp10 are functionally non-redundant and share unique characteristics that have not been described for the PIAS family. Further investigation into the functional roles of these two PIAS-like proteins may help to better understand prostate cancer progression, and yield possible new targets for therapeutic intervention.

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