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Homologous SV40 RNA trans-splicing: Special case or prime example of viral RNA trans-splicing?

机译:同源SV40 RNA转拼:病毒RNA转拼的特例或主要例子?

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摘要

To date the Simian Virus 40 (SV40) is the only proven example of a virus that recruits the mechanism of RNA trans-splicing to diversify its sequences and gene products. Thereby, two identical viral transcripts are efficiently joined by homologous trans-splicing triggering the formation of a highly transforming 100 kDa super T antigen. Sequences of other viruses including HIV-1 and the human adenovirus type 5 were reported to be involved in heterologous trans-splicing towards cellular or viral sequences but the meaning of these events remains unclear. We computationally and experimentally investigated molecular features associated with viral RNA trans-splicing and identified a common pattern: Viral RNA trans-splicing occurs between strong cryptic or regular viral splice sites and strong regular or cryptic splice sites of the trans-splice partner sequences. The majority of these splice sites are supported by exonic splice enhancers. Splice sites that could compete with the trans-splicing sites for cis-splice reactions are weaker or inexistent. Finally, all but one of the trans-splice reactions seem to be facilitated by one or more complementary binding domains of 11 to 16 nucleotides in length which, however occur with a statistical probability close to one for the given length of the involved sequences. The chimeric RNAs generated via heterologous viral RNA trans-splicing either did not lead to fusion proteins or led to proteins of unknown function. Our data suggest that distinct viral RNAs are highly susceptible to trans-splicing and that heterologous viral trans-splicing, unlike homologous SV40 trans-splicing, represents a chance event.
机译:迄今为止,猿猴病毒40(SV40)是唯一经过证实的病毒实例,该病毒募集了RNA转拼机制以使其序列和基因产物多样化。从而,两个相同的病毒转录本通过同源反式剪接有效连接,从而触发了高度转化的100 kDa超级T抗原的形成。据报道,包括HIV-1和5型人类腺病毒在内的其他病毒的序列也参与了向细胞或病毒序列的异源反式剪接,但这些事件的含义尚不清楚。我们通过计算和实验研究了与病毒RNA反式剪接相关的分子特征,并确定了一个共同的模式:病毒RNA反式剪接发生在强的隐性或规则性病毒剪接位点与强性的常规或隐性剪接位点之间。这些剪接位点的大部分由外显子剪接增强子支持。可能与反式剪接位点竞争顺式剪接反应的剪接位点较弱或不存在。最后,除一个剪接反应外,除一个剪接反应外,似乎都由一个或多个长度为11至16个核苷酸的互补结合域所促进,但是对于所涉及序列的给定长度,其统计概率接近于一个。通过异源病毒RNA转拼产生的嵌合RNA不会导致融合蛋白或功能未知的蛋白。我们的数据表明,不同的病毒RNA对转拼高度敏感,与同源SV40转拼不同,异源病毒转拼代表了偶然事件。

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