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关于尼多病毒亚基因组mRNA合成调控的新见解。

New insights about the regulation of Nidovirus subgenomic mRNA synthesis.

作者信息

Di Han, McIntyre Ayisha A, Brinton Margo A

机构信息

Department of Biology, Georgia State University, P.O. Box 4010, Atlanta, GA 30303, USA.

Department of Biology, Georgia State University, P.O. Box 4010, Atlanta, GA 30303, USA.

出版信息

Virology. 2018 Apr;517:38-43. doi: 10.1016/j.virol.2018.01.026. Epub 2018 Feb 21.

Abstract

The members of the Order Nidovirales share a similar genome organization with two overlapping nonstructural polyproteins encoded in the 5' two-thirds and the structural proteins encoded in the 3' third. They also express their 3' region proteins from a nested set of 3' co-terminal subgenomic messenger RNAs (sg mRNAs). Some but not all of the Nidovirus sg mRNAs also have a common 5' leader sequence that is acquired by a discontinuous RNA synthesis mechanism regulated by multiple 3' body transcription regulating sequences (TRSs) and the 5' leader TRS. Initial studies detected a single major body TRS for each 3' sg mRNA with a few alternative functional TRSs reported. The recent application of advanced techniques, such as next generation sequencing and ribosomal profiling, in studies of arteriviruses and coronaviruses has revealed an expanded sg mRNA transcriptome and coding capacity.

摘要

尼多病毒目成员具有相似的基因组结构,其5'端三分之二区域编码两个重叠的非结构多聚蛋白,3'端三分之一区域编码结构蛋白。它们还通过一组嵌套的3'共末端亚基因组信使核糖核酸(sg mRNA)来表达其3'区域蛋白。部分但并非所有尼多病毒的sg mRNA也具有一个共同的5'前导序列,该序列通过由多个3'主体转录调控序列(TRS)和5'前导TRS调控的不连续RNA合成机制获得。最初的研究检测到每个3' sg mRNA有一个单一的主要主体TRS,并报道了一些替代功能性TRS。近期,先进技术如新一代测序和核糖体分析在动脉炎病毒和冠状病毒研究中的应用,揭示了一个扩展的sg mRNA转录组和编码能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e61e/7112062/7dcfe78af4b9/gr1_lrg.jpg

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