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HIV-1整合酶催化核心结构域内C末端区域对酵母致死性、染色质结合及病毒复制的作用。

Contribution of the C-terminal region within the catalytic core domain of HIV-1 integrase to yeast lethality, chromatin binding and viral replication.

作者信息

Xu Zaikun, Zheng Yingfeng, Ao Zhujun, Clement Martin, Mouland Andrew J, Kalpana Ganjam V, Belhumeur Pierre, Cohen Eric A, Yao Xiaojian

机构信息

Laboratory of Molecular Human Retrovirology, Department of Medical Microbiology, University of Manitoba, 508-730 William Avenue, Winnipeg, R3E 0W3, Canada.

出版信息

Retrovirology. 2008 Nov 14;5:102. doi: 10.1186/1742-4690-5-102.

Abstract

BACKGROUND

HIV-1 integrase (IN) is a key viral enzymatic molecule required for the integration of the viral cDNA into the genome. Additionally, HIV-1 IN has been shown to play important roles in several other steps during the viral life cycle, including reverse transcription, nuclear import and chromatin targeting. Interestingly, previous studies have demonstrated that the expression of HIV-1 IN induces the lethal phenotype in some strains of Saccharomyces cerevisiae. In this study, we performed mutagenic analyses of the C-terminal region of the catalytic core domain of HIV-1 IN in order to delineate the critical amino acid(s) and/or motif(s) required for the induction of the lethal phenotype in the yeast strain HP16, and to further elucidate the molecular mechanism which causes this phenotype.

RESULTS

Our study identified three HIV-1 IN mutants, V165A, A179P and KR186,7AA, located in the C-terminal region of the catalytic core domain of IN that do not induce the lethal phenotype in yeast. Chromatin binding assays in yeast and mammalian cells demonstrated that these IN mutants were impaired for the ability to bind chromatin. Additionally, we determined that while these IN mutants failed to interact with LEDGF/p75, they retained the ability to bind Integrase interactor 1. Furthermore, we observed that VSV-G-pseudotyped HIV-1 containing these IN mutants was unable to replicate in the C8166 T cell line and this defect was partially rescued by complementation with the catalytically inactive D64E IN mutant.

CONCLUSION

Overall, this study demonstrates that three mutations located in the C-terminal region of the catalytic core domain of HIV-1 IN inhibit the IN-induced lethal phenotype in yeast by inhibiting the binding of IN to the host chromatin. These results demonstrate that the C-terminal region of the catalytic core domain of HIV-1 IN is important for binding to host chromatin and is crucial for both viral replication and the promotion of the IN-induced lethal phenotype in yeast.

摘要

背景

HIV-1整合酶(IN)是病毒cDNA整合到基因组中所需的关键病毒酶分子。此外,HIV-1 IN已被证明在病毒生命周期的其他几个步骤中发挥重要作用,包括逆转录、核输入和染色质靶向。有趣的是,先前的研究表明,HIV-1 IN的表达在某些酿酒酵母菌株中诱导致死表型。在本研究中,我们对HIV-1 IN催化核心结构域的C末端区域进行了诱变分析,以确定在酵母菌株HP16中诱导致死表型所需的关键氨基酸和/或基序,并进一步阐明导致这种表型的分子机制。

结果

我们的研究鉴定出三个HIV-1 IN突变体,V165A、A179P和KR186,7AA,位于IN催化核心结构域的C末端区域,它们在酵母中不诱导致死表型。酵母和哺乳动物细胞中的染色质结合试验表明,这些IN突变体结合染色质的能力受损。此外,我们确定,虽然这些IN突变体未能与LEDGF/p75相互作用,但它们保留了结合整合酶相互作用因子1的能力。此外,我们观察到含有这些IN突变体的VSV-G假型HIV-1无法在C8166 T细胞系中复制,并且通过与催化无活性的D64E IN突变体互补,这种缺陷得到了部分挽救。

结论

总体而言,本研究表明,位于HIV-1 IN催化核心结构域C末端区域的三个突变通过抑制IN与宿主染色质的结合来抑制酵母中IN诱导的致死表型。这些结果表明,HIV-1 IN催化核心结构域的C末端区域对于与宿主染色质的结合很重要,并且对于病毒复制以及酵母中IN诱导的致死表型的促进都至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caa7/2615443/5146f7cfd2ce/1742-4690-5-102-1.jpg

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