The HIV-1 Transcriptional Program: From Initiation to Elongation Control.

IF 4.7 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Iván D'Orso
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Abstract

A large body of work in the last four decades has revealed the key pillars of HIV-1 transcription control at the initiation and elongation steps. Here, I provide a recount of this collective knowledge starting with the genomic elements (DNA and nascent TAR RNA stem-loop) and transcription factors (cellular and the viral transactivator Tat), and later transitioning to the assembly and regulation of transcription initiation and elongation complexes, and the role of chromatin structure. Compelling evidence support a core HIV-1 transcriptional program regulated by the sequential and concerted action of cellular transcription factors and Tat to promote initiation and sustain elongation, highlighting the efficiency of a small virus to take over its host to produce the high levels of transcription required for viral replication. I summarize new advances including the use of CRISPR-Cas9, genetic tools for acute factor depletion, and imaging to study transcriptional dynamics, bursting and the progression through the multiple phases of the transcriptional cycle. Finally, I describe current challenges to future major advances and discuss areas that deserve more attention to both bolster our basic knowledge of the core HIV-1 transcriptional program and open up new therapeutic opportunities.

Abstract Image

HIV-1 转录程序:从启动到延伸控制
过去四十年的大量研究揭示了 HIV-1 转录在起始和延伸阶段的关键控制支柱。在此,我将从基因组元素(DNA 和新生 TAR RNA 干环)和转录因子(细胞和病毒转录因子 Tat)入手,对这些集体知识进行回顾,然后过渡到转录起始和延伸复合物的组装和调控,以及染色质结构的作用。令人信服的证据表明,HIV-1 的核心转录程序是由细胞转录因子和 Tat 的连续协同作用调控的,以促进启动和维持延伸,突显了一种小型病毒接管宿主以产生病毒复制所需的高水平转录的效率。我总结了新的进展,包括使用 CRISPR-Cas9、急性因子耗竭的遗传工具和成像技术来研究转录动态、突变和转录周期多个阶段的进展。最后,我将介绍未来重大进展所面临的挑战,并讨论值得更多关注的领域,以加强我们对 HIV-1 核心转录程序的基本了解,并开辟新的治疗机会。
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来源期刊
Journal of Molecular Biology
Journal of Molecular Biology 生物-生化与分子生物学
CiteScore
11.30
自引率
1.80%
发文量
412
审稿时长
28 days
期刊介绍: Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions. Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.
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