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1型人类免疫缺陷病毒Tat不会在灵长类细胞的细胞核或细胞质中反式激活成熟的反式作用应答区域RNA种类。

Human immunodeficiency virus type 1 Tat does not transactivate mature trans-acting responsive region RNA species in the nucleus or cytoplasm of primate cells.

作者信息

Chin D J, Selby M J, Peterlin B M

机构信息

Department of Pharmacology, University of California, San Francisco 94143.

出版信息

J Virol. 1991 Apr;65(4):1758-64. doi: 10.1128/JVI.65.4.1758-1764.1991.

Abstract

Human immunodeficiency virus (HIV)-encoded transactivator Tat is essential for viral gene expression and replication. By interacting with a nascent RNA stem-loop called the trans-acting responsive region (TAR). Tat increases rates of initiation and/or elongation of HIV transcription. Several reports have also suggested that Tat has additional effects on mature HIV RNA species including modification of primary transcripts in the nucleus and their increased translation in the cytoplasm. These posttranscriptional effects are most pronounced in the Xenopus oocyte. To investigate directly whether Tat has similar effects on viral transcripts in cells that are permissive for HIV replication, we cotransfected and microinjected human and monkey cells with Tat and TAR in the form of DNA or RNA. Whereas Tat transactivated TAR DNA targets, it did not transactivate TAR RNA targets in the nucleus of microinjected cells or in the cytoplasm of transfected cells. We conclude that in cells permissive for viral replication, Tat exerts its effect primarily at the level of HIV transcription.

摘要

人类免疫缺陷病毒(HIV)编码的反式激活因子Tat对病毒基因表达和复制至关重要。通过与一种称为反式作用应答区域(TAR)的新生RNA茎环相互作用,Tat提高了HIV转录的起始和/或延伸速率。一些报告还表明,Tat对成熟的HIV RNA种类有额外影响,包括对细胞核中初级转录本的修饰及其在细胞质中翻译的增加。这些转录后效应在非洲爪蟾卵母细胞中最为明显。为了直接研究Tat对允许HIV复制的细胞中的病毒转录本是否有类似影响,我们将Tat和TAR以DNA或RNA的形式共转染并显微注射到人和猴细胞中。虽然Tat可反式激活TAR DNA靶点,但它在显微注射细胞的细胞核或转染细胞的细胞质中均未反式激活TAR RNA靶点。我们得出结论,在允许病毒复制的细胞中,Tat主要在HIV转录水平发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96d4/239982/85c9fd2625d0/jvirol00047-0105-a.jpg

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