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HIV-1 splicing is controlled by local RNA structure and binding of splicing regulatory proteins at the major 5' splice site

机译:HIV-1剪接受局部RNA结构和主要5'剪接位点的剪接调节蛋白结合的控制

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摘要

The 5' leader region of the human immunodeficiency virus 1 (HIV-1) RNA genome contains the major 5' splice site (ss) that is used in the production of the many spliced viral RNAs. This splice-donor (SD) region can fold into a stable stem-loop structure and the thermodynamic stability of this RNA hairpin influences splicing efficiency. In addition, splicing may be modulated by binding of splicing regulatory (SR) proteins, in particular SF2/ASF (SRSF1), SC35 (SRSF2), SRp40 (SRSF5) and SRp55 (SRSF6), to sequence elements in the SD region. The role of RNA structure and SR protein binding in splicing control was previously studied by functional analysis of mutant SD sequences. The interpretation of these studies was complicated by the fact that most mutations simultaneously affect both structure and sequence elements. We therefore tried to disentangle the contribution of these two variables by designing more precise SD region mutants with a single effect on either the sequence or the structure. The current analysis indicates that HIV-1 splicing at the major 5'ss is modulated by both the stability of the local RNA structure and the binding of splicing regulatory proteins
机译:人类免疫缺陷病毒1(HIV-1)RNA基因组的5'前导区含有主要的5'剪接位点,可用于生产许多剪接的病毒RNA。该剪接供体(SD)区域可以折叠成稳定的茎环结构,并且此RNA发夹的热力学稳定性会影响剪接效率。另外,可以通过将剪接调节(SR)蛋白,特别是SF2 / ASF(SRSF1),SC35(SRSF2),SRp40(SRSF5)和SRp55(SRSF6)结合至SD区域中的序列元件来调节剪接。 RNA结构和SR蛋白结合在剪接控制中的作用以前已通过突变SD序列的功能分析进行了研究。大多数突变同时影响结构和序列元素,使这些研究的解释变得复杂。因此,我们试图通过设计对序列或结构具有单一影响的更精确的SD区突变体来区分这两个变量的作用。当前的分析表明,在主要5年代剪接的HIV-1受局部RNA结构的稳定性和剪接调节蛋白的结合的调节

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