HIV Tat represses transcription of the β2-microglobulin promoter

被引:37
作者
Carroll, IR [1 ]
Wang, J [1 ]
Howcroft, TK [1 ]
Singer, DS [1 ]
机构
[1] NCI, Mol Regulat Sect, Expt Immunol Branch, NIH, Bethesda, MD 20892 USA
关键词
transcription; HIV Tat; beta(2)-microglobulin; promoter; LTR;
D O I
10.1016/S0161-5890(98)00107-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The MHC class I complex, which binds and presents peptide antigen, is composed of a class I heavy chain and the beta(2)-microglobulin light chain. HIV-1, which induces a profound immunodeficiency in infected individuals, encodes proteins that cause decreased expression of class I heavy chain. We now report that the HIV Tat protein, which is a potent transactivator of viral transcription, is also a potent repressor of the beta(2)-microglobulin gene. Repression is mediated through the basal promoter of the beta(2)-microglobulin gene, which is shown to be predominantly regulated by an initiator element. Tat repression is further augmented by the short viral transcript, TAR, which interacts with Tat. Tat-mediated repression of beta(2)-microglobulin expression, together with its known repression of class I gene transcription, provides an effective mechanism by which HIV could prevent cell surface expression of the MHC class I complex and avoid immune surveillance. Published by Elsevier Science Ltd.
引用
收藏
页码:1171 / 1178
页数:8
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