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HIV-1 TAR RNA发夹结构的顶端环通过一个跨环碱基对得以稳定。

The apical loop of the HIV-1 TAR RNA hairpin is stabilized by a cross-loop base pair.

作者信息

Kulinski Tadeusz, Olejniczak Mikolaj, Huthoff Hendrik, Bielecki Lukasz, Pachulska-Wieczorek Katarzyna, Das Atze T, Berkhout Ben, Adamiak Ryszard W

机构信息

Institute of Bioorganic Chemistry, Polish Academy of Sciences, Noskowskiego 12-14, 61-704 Poznañ, Poland.

出版信息

J Biol Chem. 2003 Oct 3;278(40):38892-901. doi: 10.1074/jbc.M301939200. Epub 2003 Jul 25.

Abstract

The TAR hairpin of the HIV-1 RNA genome is indispensable for trans-activation of the viral promoter and virus replication. The TAR structure has been studied extensively, but most attention has been directed at the three-nucleotide bulge that constitutes the binding site of the viral Tat protein. In contrast, the conformational properties of the apical loop have remained elusive. We performed biochemical studies and molecular dynamics simulations, which indicate that the TAR loop is structured and stabilized by a cross-loop base pair between residues C30 and G34. Mutational disruption of the cross-loop base pair results in reduced Tat response of the LTR promoter, which can be rescued by compensatory mutations that restore the base pair. Thus, Tat-mediated transcriptional activation depends on the structure of the TAR apical loop. The C30-G34 cross-loop base pair classes TAR in a growing family of hairpins with a structured loop that was recently identified in ribosomal RNA, tRNA, and several viral and cellular mRNAs.

摘要

HIV-1 RNA基因组的TAR发夹结构对于病毒启动子的反式激活和病毒复制不可或缺。TAR结构已得到广泛研究,但大部分注意力都集中在构成病毒Tat蛋白结合位点的三核苷酸凸起上。相比之下,顶端环的构象特性仍不清楚。我们进行了生化研究和分子动力学模拟,结果表明TAR环是由C30和G34残基之间的跨环碱基对构成并稳定的。跨环碱基对的突变破坏会导致LTR启动子的Tat反应降低,而恢复碱基对的补偿性突变可以挽救这种情况。因此,Tat介导的转录激活取决于TAR顶端环的结构。C30-G34跨环碱基对将TAR归类于一个不断增加的发夹家族,该家族的环结构在核糖体RNA、tRNA以及几种病毒和细胞mRNA中最近被发现。

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