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利什曼原虫RNA病毒1的分子结构

Molecular organization of Leishmania RNA virus 1.

作者信息

Stuart K D, Weeks R, Guilbride L, Myler P J

机构信息

Seattle Biomedical Research Institute, WA 98109-1651.

出版信息

Proc Natl Acad Sci U S A. 1992 Sep 15;89(18):8596-600. doi: 10.1073/pnas.89.18.8596.

Abstract

The complete 5284-nucleotide sequence of the double-stranded RNA genome of Leishmania RNA virus 1 (LRV1) was determined and contains three open reading frames (ORFs) on the plus (+) (mRNA) strand. The predicted amino acid sequence of ORF3 has motifs characteristic of viral RNA-dependent RNA polymerases. ORF2, which may encode the major viral coat protein, overlaps ORF3 by 71 nucleotides, suggesting a +1 translational frameshift to produce a gag-pol type of fusion protein. Two alternative models for the frameshift are presented. The 5' splice leader sequence of kinetoplastid mRNAs is not in LRV1 RNA. This suggests that the 450-base region at the 5' end of the LRV1 (+)-strand, which contains ORF1 and is highly conserved among viral strains, does not encode protein but has a role in initiation of translation and/or RNA stability. The similarity of LRV1 genomic organization, replication cycle, and RNA-dependent RNA polymerase sequence to those of the yeast virus ScV L-A suggests a common ancestral origin. The possibility that LRV1 affects pathogenesis in leishmaniasis is intriguing.

摘要

利什曼原虫RNA病毒1(LRV1)双链RNA基因组完整的5284个核苷酸序列已被确定,其正义(+)(mRNA)链上含有三个开放阅读框(ORF)。ORF3预测的氨基酸序列具有病毒RNA依赖性RNA聚合酶的特征基序。可能编码主要病毒衣壳蛋白的ORF2与ORF3重叠71个核苷酸,提示发生+1移码以产生gag-pol型融合蛋白。文中提出了两种移码的替代模型。动质体mRNA的5'剪接前导序列不在LRV1 RNA中。这表明LRV1正义链5'端含ORF1且在病毒株间高度保守的450个碱基区域不编码蛋白质,但在翻译起始和/或RNA稳定性方面起作用。LRV1基因组组织、复制周期及RNA依赖性RNA聚合酶序列与酵母病毒ScV L-A的相似性提示它们有共同的祖先起源。LRV1影响利什曼病发病机制的可能性很有趣。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d4d/49967/c7169ea54aa6/pnas01092-0199-a.jpg

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