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在前列腺癌中通过p68 DEAD盒RNA解旋酶雄激素受体共激活因子将转录与RNA加工偶联起来。

Coupling transcription to RNA processing via the p68 DEAD box RNA helicase androgen receptor co-activator in prostate cancer.

作者信息

Clark Emma L, Fuller-Pace Frances V, Elliott David J, Robson Craig N

机构信息

Northern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne NE2 4AD, UK.

出版信息

Biochem Soc Trans. 2008 Jun;36(Pt 3):546-7. doi: 10.1042/BST0360546.

Abstract

The mechanisms involved in the transition from androgen-dependent to androgen-independent PCa (prostate cancer) remain largely undefined. The AR (androgen receptor) is an androgen-dependent transcription factor and is thought to play an important role in the development of both androgen-dependent and -independent prostatic malignancy. AR-mediated transcription is regulated by the binding of various cofactor proteins to the AR that facilitate transcriptional initiation and elongation. Elucidating the mechanisms by which cofactors regulate AR transcriptional activity may reveal the therapeutic potential of cofactors in PCa. Current models of gene expression indicate that transcription and RNA processing are tightly coupled. In this review, we discuss how the ATP-dependent DEAD box RNA helicase p68, which has established roles in transcription and RNA processing, may function as an 'adaptor' or coupling protein to facilitate cross-talk between transcription and RNA processing in AR-regulated genes by controlling the rate of transcriptional initiation/elongation.

摘要

从雄激素依赖型前列腺癌(PCa)转变为雄激素非依赖型前列腺癌所涉及的机制在很大程度上仍不明确。雄激素受体(AR)是一种雄激素依赖型转录因子,被认为在雄激素依赖型和非依赖型前列腺恶性肿瘤的发展中都起着重要作用。AR介导的转录受多种辅助因子蛋白与AR结合的调控,这些辅助因子促进转录起始和延伸。阐明辅助因子调节AR转录活性的机制可能揭示其在前列腺癌中的治疗潜力。当前的基因表达模型表明转录和RNA加工紧密偶联。在本综述中,我们讨论了在转录和RNA加工中已明确发挥作用的ATP依赖型DEAD盒RNA解旋酶p68如何作为一种“衔接子”或偶联蛋白,通过控制转录起始/延伸速率来促进AR调控基因转录与RNA加工之间的相互作用。

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