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人类免疫缺陷病毒1型(HIV-1)病毒体相关蛋白Vpr是人类糖皮质激素受体的一种共激活因子。

The HIV-1 virion-associated protein vpr is a coactivator of the human glucocorticoid receptor.

作者信息

Kino T, Gragerov A, Kopp J B, Stauber R H, Pavlakis G N, Chrousos G P

机构信息

Section on Pediatric Endocrinology, Developmental Endocrinology Branch, National Institute of Child Health and Human Development, Bethesda, MD 20892, USA.

出版信息

J Exp Med. 1999 Jan 4;189(1):51-62. doi: 10.1084/jem.189.1.51.

Abstract

The HIV-1 virion-associated accessory protein Vpr affects both viral replication and cellular transcription, proliferation, and differentiation. We report that Vpr enhances the activity of glucocorticoids in lymphoid and muscle-derived cell lines by interacting directly with the glucocorticoid receptor and general transcription factors, acting as a coactivator. Vpr contains the signature motif LXXLL also present in cellular nuclear receptor coactivators, such as steroid receptor coactivator 1 and p300/CREB-binding protein, which mediates their interaction with the glucocorticoid and other nuclear hormone receptors. A mutant Vpr molecule with disruption of this coactivator signature motif lost its ability to influence transcription of glucocorticoid-responsive genes and became a dominant-negative inhibitor of Vpr, possibly by retaining its general transcription factor-binding activities. The glucocorticoid coactivator activity of Vpr may contribute to increased tissue glucocorticoid sensitivity in the absence of hypercortisolism and to the pathogenesis of AIDS.

摘要

HIV-1病毒体相关辅助蛋白Vpr既影响病毒复制,也影响细胞转录、增殖和分化。我们报告称,Vpr通过直接与糖皮质激素受体和一般转录因子相互作用,作为共激活因子,增强了糖皮质激素在淋巴和肌肉来源细胞系中的活性。Vpr含有细胞内核受体共激活因子(如类固醇受体共激活因子1和p300/CREB结合蛋白)中也存在的标志性基序LXXLL,该基序介导它们与糖皮质激素及其他核激素受体的相互作用。一个破坏了这种共激活因子标志性基序的Vpr突变分子失去了影响糖皮质激素反应性基因转录的能力,并成为Vpr的显性负性抑制剂,这可能是通过保留其一般转录因子结合活性实现的。Vpr的糖皮质激素共激活因子活性可能在无皮质醇增多症的情况下导致组织对糖皮质激素敏感性增加,并参与艾滋病的发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ec2/1887689/734ddc934341/JEM981442.f1.jpg

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