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铰链区中的 629RKLKK633 基序在多个水平上控制雄激素受体。

A 629RKLKK633 motif in the hinge region controls the androgen receptor at multiple levels.

机构信息

Molecular Endocrinology Laboratory, Department of Molecular Cell Biology, Catholic University of Leuven, Campus Gasthuisberg O&N1, Herestraat 49, Box 901, 3000, Leuven, Belgium.

出版信息

Cell Mol Life Sci. 2010 Jun;67(11):1919-27. doi: 10.1007/s00018-010-0302-1. Epub 2010 Feb 26.

Abstract

The androgen receptor protein has specific domains involved in DNA binding, ligand binding, and transactivation, whose activities need to be integrated during transcription activation. The hinge region, more particular a (629)RKLKK(633) motif, seems to play a crucial role in this process. Indeed, although the motif is not part of the DNA-binding domain, its positive residues are involved in optimal DNA binding and nuclear translocation as shown by mutation analysis. When the mutated ARs are forced into the nucleus, however, the residues seem to play different roles in transactivation. Moreover, we show by FRAP analysis that during activation, the AR is distributed in the nucleus in a mobile and two immobile fractions, and that mutations in the (629)RKLKK(633) motif affect the distribution of the AR over these three intranuclear fractions. Taken together, the (629)RKLKK(633) motif is a multifunctional motif that integrates nuclear localization, receptor stability, DNA binding, transactivation potential and intranuclear mobility.

摘要

雄激素受体蛋白具有特定的结构域,参与 DNA 结合、配体结合和转录激活,其活性需要在转录激活过程中整合。铰链区,更具体地说是 (629)RKLKK(633) 基序,似乎在这个过程中起着关键作用。事实上,尽管该基序不是 DNA 结合域的一部分,但突变分析表明,其阳性残基参与了最佳的 DNA 结合和核转位。然而,当突变的 AR 被强制进入细胞核时,这些残基在转录激活中似乎发挥不同的作用。此外,我们通过 FRAP 分析表明,在激活过程中,AR 在细胞核中以可移动和两个不可移动的分数分布,并且 (629)RKLKK(633) 基序中的突变会影响 AR 在这三个核内分数中的分布。总之,(629)RKLKK(633) 基序是一个多功能基序,整合了核定位、受体稳定性、DNA 结合、转录激活潜力和核内迁移性。

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