相分离介导的雄激素受体核下区隔化

IF 5.1 2区 生物学 Q2 CELL BIOLOGY Cells Pub Date : 2024-10-13 DOI:10.3390/cells13201693
Selçuk Yavuz, Tsion E Abraham, Adriaan B Houtsmuller, Martin E van Royen
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引用次数: 0

摘要

雄激素受体(AR)是转录因子核类固醇激素受体家族的成员,它不仅在男性表型的形成过程中起着关键作用,而且在前列腺癌的发生和生长过程中也起着关键作用。虽然对 AR 的结构以及 AR 与核心调控因子和染色质的相互作用进行了详细研究,从而提高了我们对 AR 在基因转录调控中的功能的认识,但对细胞核中显微镜下可辨认的 AR 病灶的时空组织和作用的研究仍然不足。这篇综述深入探讨了 AR 病灶形成的分子机制,重点是液-液相分离及其在转录位点的核内空间组织 AR 及其结合伙伴的作用,以及三维基因组组织对 AR 介导的基因转录的影响。
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Phase Separation Mediated Sub-Nuclear Compartmentalization of Androgen Receptors.

The androgen receptor (AR), a member of the nuclear steroid hormone receptor family of transcription factors, plays a crucial role not only in the development of the male phenotype but also in the development and growth of prostate cancer. While AR structure and AR interactions with coregulators and chromatin have been studied in detail, improving our understanding of AR function in gene transcription regulation, the spatio-temporal organization and the role of microscopically discernible AR foci in the nucleus are still underexplored. This review delves into the molecular mechanisms underlying AR foci formation, focusing on liquid-liquid phase separation and its role in spatially organizing ARs and their binding partners within the nucleus at transcription sites, as well as the influence of 3D-genome organization on AR-mediated gene transcription.

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来源期刊
Cells
Cells Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
CiteScore
9.90
自引率
5.00%
发文量
3472
审稿时长
16 days
期刊介绍: Cells (ISSN 2073-4409) is an international, peer-reviewed open access journal which provides an advanced forum for studies related to cell biology, molecular biology and biophysics. It publishes reviews, research articles, communications and technical notes. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. Full experimental and/or methodical details must be provided.
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