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通过特定突变探究噬菌体 phi 29 原头部 RNA 的结构

Probing the structure of bacteriophage phi 29 prohead RNA with specific mutations.

作者信息

Reid R J, Zhang F, Benson S, Anderson D

机构信息

Department of Genetics and Cell Biology, University of Minnesota, Minneapolis 55455.

出版信息

J Biol Chem. 1994 Jul 15;269(28):18656-61.

PMID:8034614
Abstract

Bacteriophage phi 29 of Bacillus subtilis packages its double-stranded DNA genome into a preformed prohead in an ATP-dependent reaction. A 174-residue phi 29-encoded RNA molecule (pRNA) is a structural component of the prohead and is essential for DNA packaging. The secondary and tertiary structures of the prohead binding site on pRNA have been probed using a series of specific mutant pRNAs and by measuring binding to RNA-free proheads and in vitro packaging of the DNA-gene product 3 (DNA.gp3) complex. A pseudoknot in pRNA inferred from phylogenetic studies was confirmed with specific mutations, and this pseudoknot was necessary for DNA.gp3 packaging activity. pRNA was truncated progressively from the 5' and 3' ends to isolate the prohead binding site, and three truncated pRNAs of 79, 71, and 62 residues retained prohead binding activity but could not reconstitute proheads for DNA.gp3 packaging. Mutation resulting in changes of the D hairpin loop and its connecting residues within the prohead binding site of pRNA and DNA packaging studies demonstrated that some alteration of secondary structure in this helix was permissible. The analyses provided further confirmation of a discrete prohead binding domain in pRNA and further delineated specific structural requirements for DNA.gp3 packaging activity which may not be required for prohead binding.

摘要

枯草芽孢杆菌的噬菌体 phi 29 通过依赖 ATP 的反应将其双链 DNA 基因组包装到预先形成的原头部中。一个由 phi 29 编码的 174 个残基的 RNA 分子(pRNA)是原头部的结构成分,对 DNA 包装至关重要。通过一系列特定的突变 pRNA,并测量其与无 RNA 的原头部的结合以及 DNA - 基因产物 3(DNA.gp3)复合物的体外包装,对 pRNA 上原头部结合位点的二级和三级结构进行了探究。从系统发育研究推断出的 pRNA 中的假结通过特定突变得到证实,并且这个假结对 DNA.gp3 的包装活性是必需的。从 5' 和 3' 末端逐步截短 pRNA 以分离原头部结合位点,三个分别含有 79、71 和 62 个残基的截短 pRNA 保留了原头部结合活性,但不能重新组装用于 DNA.gp3 包装的原头部。导致 pRNA 原头部结合位点内 D 发夹环及其连接残基发生变化的突变以及 DNA 包装研究表明,该螺旋中二级结构的某些改变是允许的。这些分析进一步证实了 pRNA 中存在一个离散的原头部结合结构域,并进一步描绘了 DNA.gp3 包装活性所需的特定结构要求,而这些要求可能不是原头部结合所必需的。

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