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Structural and functional analysis of the Rous Sarcoma virus negative regulator of splicing and demonstration of its activation by the 9G8 SR protein

机译:劳斯肉瘤病毒剪接负调控因子的结构和功能分析,并证明其被9G8 SR蛋白激活

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摘要

Retroviruses require both spliced and unspliced RNAs for replication. Accumulation of Rous Sarcoma virus (RSV) unspliced RNA depends upon the negative regulator of splicing (NRS). Its 5'-part is considered as an ESE binding SR proteins. Its 3'-part contains a decoy 5'-splice site (ss), which inhibits splicing at the bona fide 5'-ss. Only the 3D structure of a small NRS fragment had been experimentally studied. Here, by chemical and enzymatic probing, we determine the 2D structure of the entire RSV NRS. Structural analysis of other avian NRSs and comparison with all sequenced avian NRSs is in favour of a phylogenetic conservation of the NRS 2D structure. By combination of approaches: (i) in vitro and in cellulo splicing assays, (ii) footprinting assays and (iii) purification and analysis of reconstituted RNP complex, we define a small NRS element retaining splicing inhibitory property. We also demonstrate the capability of the SR protein 9G8 to increase NRS activity in vitro and in cellulo. Altogether these data bring new insights on how NRS fine tune splicing activity.
机译:逆转录病毒需要剪接和未剪接的RNA才能复制。劳斯肉瘤病毒(RSV)未剪接的RNA的积累取决于剪接的负调控因子(NRS)。它的5'部分被认为是结合ESE的SR蛋白。其3'部分包含诱骗的5'-剪接位点(ss),其抑制了真正的5'-ss的剪接。仅对NRS小片段的3D结构进行了实验研究。在这里,通过化学和酶促探测,我们确定了整个RSV NRS的2D结构。其他禽类NRS的结构分析以及与所有测序的禽类NRS的比较有利于NRS 2D结构的系统发育保守。通过方法的组合:(i)体外和纤维素剪接测定,(ii)足迹测定和(iii)重组RNP复合物的纯化和分析,我们定义了保留剪接抑制特性的小NRS元件。我们还证明了SR蛋白9G8在体外和纤维素中增加NRS活性的能力。总而言之,这些数据带来了有关NRS如何微调拼接活动的新见解。

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