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禽呼肠孤病毒RNA 2复制的顺式作用要求

cis-acting requirements for the replication of flock house virus RNA 2.

作者信息

Ball L A, Li Y

机构信息

Department of Microbiology, University of Alabama, Birmingham 35294-0005.

出版信息

J Virol. 1993 Jun;67(6):3544-51. doi: 10.1128/JVI.67.6.3544-3551.1993.

DOI:10.1128/JVI.67.6.3544-3551.1993
PMID:8497063
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC237701/
Abstract

To examine the cis-acting requirements for RNA replication, a cDNA clone of flock house virus (FHV) RNA 2 was transfected into baby hamster kidney cells and transcribed to yield RNAs that had terminal extensions of different lengths or that lacked internal regions of the molecule. These RNAs were tested for their ability to be replicated by FHV replicase that was provided by cotransfection of purified FHV RNA 1. The results showed that RNA replication was inhibited by terminal extensions, particularly those at the 5' end of the RNA, despite the fact that these extensions were corrected during RNA replication. A negative-sense transcript with a 12-nucleotide 3' extension was replicated to produce a positive-sense RNA that had the correct 5' end, showing that the replicase could select its correct initiation site from within a longer template. A uridine residue at the second position of the positive strand was an important determinant of template activity. RNA molecules with large internal deletions that amounted to almost 50% of the 1,400 nucleotides of RNA 2 replicated as efficiently as full-length molecules, but only if they contained an internal region that lay between nucleotides 538 and 616. Thirty-six spontaneous deletions of RNA 2 that arose during sequential replicative passages all conserved the same internal region of the molecule. These results establish that both terminal and internal regions of FHV RNA 2 play essential roles in making the molecule a competent template for replication.

摘要

为了研究RNA复制的顺式作用需求,将禽呼肠孤病毒(FHV)RNA 2的cDNA克隆转染至幼仓鼠肾细胞中,并转录产生具有不同长度末端延伸或缺少分子内部区域的RNA。通过共转染纯化的FHV RNA 1提供FHV复制酶,测试这些RNA的复制能力。结果表明,末端延伸,特别是RNA 5'端的延伸,会抑制RNA复制,尽管这些延伸在RNA复制过程中会被校正。一个具有12个核苷酸3'延伸的负义转录本被复制产生具有正确5'端的正义RNA,这表明复制酶可以从更长的模板中选择其正确的起始位点。正义链第二位的尿苷残基是模板活性的重要决定因素。内部缺失几乎占RNA 2的1400个核苷酸的50%的RNA分子,与全长分子一样有效地进行复制,但前提是它们包含位于核苷酸538和616之间的内部区域。在连续复制传代过程中出现的36个RNA 2的自发缺失都保留了分子的相同内部区域。这些结果表明,FHV RNA 2的末端和内部区域在使该分子成为有能力的复制模板方面都起着至关重要的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf47/237701/72eb7f920de0/jvirol00027-0601-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf47/237701/35c5c8f2aeb3/jvirol00027-0598-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf47/237701/17f421594973/jvirol00027-0599-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf47/237701/aa611a3aa2a0/jvirol00027-0599-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf47/237701/9308626d7bd3/jvirol00027-0600-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf47/237701/72eb7f920de0/jvirol00027-0601-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf47/237701/35c5c8f2aeb3/jvirol00027-0598-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf47/237701/17f421594973/jvirol00027-0599-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf47/237701/aa611a3aa2a0/jvirol00027-0599-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf47/237701/9308626d7bd3/jvirol00027-0600-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf47/237701/72eb7f920de0/jvirol00027-0601-a.jpg

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