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Posttranslational Modifications of HIV-1 Integrase by Various Cellular Proteins during Viral Replication

机译:病毒复制过程中各种细胞蛋白对HIV-1整合酶的翻译后修饰。

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摘要

HIV-1 integrase (IN) is a key viral enzyme during HIV-1 replication that catalyzes the insertion of viral DNA into the host genome. Recent studies have provided important insights into the multiple posttranslational modifications (PTMs) of IN (e.g., ubiquitination, SUMOylation, acetylation and phosphorylation), which regulate its multifaceted functions. A number of host cellular proteins, including Lens Epithelium‑derived Growth factor (LEDGF/p75), p300 and Ku70 have been shown to interact with IN and be involved in the PTM process of IN, either facilitating or counteracting the IN PTMs. Although previous studies have revealed much about the important roles of IN PTMs, how IN functions are fine-tuned by these PTMs under the physiological setting still needs to be determined. Here, we review the advances in the understanding of the mechanisms and roles of multiple IN PTMs.
机译:HIV-1整合酶(IN)是HIV-1复制过程中的一种关键病毒酶,可催化病毒DNA插入宿主基因组。最近的研究提供了对IN的多个翻译后修饰(PTM)(例如泛素化,SUMO酰化,乙酰化和磷酸化)的重要见解,它们调节了其多方面的功能。已显示许多宿主细胞蛋白,包括晶状体上皮细胞生长因子(LEDGF / p75),p300和Ku70与IN相互作用,并参与IN的PTM过程,从而促进或抵消IN PTM。尽管先前的研究已经揭示了许多有关IN PTM的重要作用,但是仍需要确定在生理环境下这些PTM如何微调IN功能。在这里,我们回顾了对多个IN PTM的机制和作用的理解的进展。

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