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双链RNA噬菌体phi6基因组包装中特异性结合的分析。

Analysis of specific binding involved in genomic packaging of the double-stranded-RNA bacteriophage phi6.

作者信息

Qiao Xueying, Qiao Jian, 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 Nov;185(21):6409-14. doi: 10.1128/JB.185.21.6409-6414.2003.

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. The packaging requires the hydrolysis of nucleoside triphosphates and takes place in the order segment S-segment M, segment L. Packaging is dependent upon unique sequences of about 200 nucleotides near the 5' ends of plus-strand transcripts of the three genomic segments. It appears that P1 is the determinant of the RNA binding sites. Directed mutation of P1 was used to locate regions that are important for genomic packaging. Specific binding of RNA to the exterior of the procapsid was dependent upon ATP, and a region that showed a high level of cross-linking to phage-specific RNA was located. Antibodies to peptide sequences were prepared, and their abilities to bind to the exterior of procapsids were determined. Sites sensitive to trypsin and to factor Xa were determined as well.

摘要

噬菌体φ6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称为原衣壳或内核的预先形成的多面体结构中。包装需要核苷三磷酸的水解,并且按照S片段-M片段-L片段的顺序进行。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。似乎P1是RNA结合位点的决定因素。利用P1的定向突变来定位对基因组包装重要的区域。RNA与原衣壳外部的特异性结合依赖于ATP,并且定位了一个与噬菌体特异性RNA高度交联的区域。制备了针对肽序列的抗体,并确定了它们与原衣壳外部结合的能力。还确定了对胰蛋白酶和因子Xa敏感的位点。

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