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具有改变包装特异性的双链RNA噬菌体phi6突变体的分离与分析。

Isolation and analysis of mutants of double-stranded-RNA bacteriophage phi6 with altered packaging specificity.

作者信息

Qiao Jian, Qiao Xueying, Sun Yang, Mindich Leonard

机构信息

Department of Microbiology, Public Health Research Institute, Newark, New Jersey 07103, USA.

出版信息

J Bacteriol. 2003 Aug;185(15):4572-7. doi: 10.1128/JB.185.15.4572-4577.2003.

Abstract

The genomes of bacteriophage phi6 and its relatives are packaged through a mechanism that involves the recognition and translocation of the three different plus strand transcripts of the segmented double-stranded RNA genomes into preformed polyhedral structures called procapsids or inner cores. This packaging requires hydrolysis of nucleoside triphosphates and takes place in the order S-M-L. Packaging is dependent on unique sequences of about 200 nucleotides near the 5' ends of plus strand transcripts of the three genomic segments. Changes in the pac sequences lead to loss of packaging ability but can be suppressed by second-site changes in RNA or amino acid changes in protein P1, the major structural protein of the procapsid. It appears that P1 is the determinant of the RNA binding sites, and it is suggested that the binding sites overlap or are conformational changes of the same domains.

摘要

噬菌体phi6及其相关病毒的基因组通过一种机制进行包装,该机制涉及将分段双链RNA基因组的三种不同正链转录本识别并转运到预先形成的多面体结构中,这些结构称为原衣壳或内核。这种包装需要核苷三磷酸的水解,并按S-M-L顺序进行。包装依赖于三个基因组片段正链转录本5'端附近约200个核苷酸的独特序列。pac序列的变化会导致包装能力丧失,但可以通过RNA中的第二位点变化或原衣壳主要结构蛋白P1中的氨基酸变化来抑制。似乎P1是RNA结合位点的决定因素,并且有人提出结合位点重叠或为相同结构域的构象变化。

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