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Transcription factors that repress hiv transcription and methods based thereon

机译:抑制HIV转录的转录因子和基于其的方法

摘要

The molecular mechanism of YY1/LSF-associated repression of HIV-1 is described herein. More particularly, an HIV transcription repressor complex containing YY1, LSF and HDAC1 is described. The invention is based on our discovery that (1) HDAC1 co-purifies with the LTR-binding YY1-LSF repressor complex; (2) the domain of YY1 that interacts with HDAC1 is required to repress the HIV-1 promoter; (3) the expression of HDAC1 augments repression of the LTR by YY1, and (4) the deacetylase inhibitor trichostatin-A blocks repression mediated by YY1. This novel link between HDAC1 recruitment and inhibition of HIV-1 expression by YY1 and LSF, in the natural context of a viral promoter integrated into chromosomal DNA, supports novel HIV therapies described herein and has significant implications for the long-term treatment of AIDS.
机译:本文描述了YY1 / LSF相关的HIV-1抑制的分子机制。更具体地,描述了包含YY1,LSF和HDAC1的HIV转录阻遏物复合物。本发明基于我们的发现,即(1)HDAC1与结合LTR的YY1-LSF阻遏物复合物共纯化; (2)抑制HIV-1启动子需要与HDAC1相互作用的YY1结构域; (3)HDAC1的表达增强了YY1对LTR的抑制,(4)脱乙酰基酶抑制剂曲古抑菌素A阻断了YY1介导的抑制。在整合入染色体DNA的病毒启动子的自然背景下,HDAC1募集与YY1和LSF对HIV-1表达的抑制之间的这种新颖联系支持本文所述的新颖HIV治疗,并且对AIDS的长期治疗具有重要意义。

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