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枯草芽孢杆菌噬菌体phi 29的小RNA介导在大肠杆菌中组装的phi 29原头部的DNA包装。

sRNA of phage phi 29 of Bacillus subtilis mediates DNA packaging of phi 29 proheads assembled in Escherichia coli.

作者信息

Guo P X, Rajagopal B S, Anderson D, Erickson S, Lee C S

机构信息

Department of Veterinary Pathobiology, Purdue University, West Lafayette, Indiana 47907.

出版信息

Virology. 1991 Nov;185(1):395-400. doi: 10.1016/0042-6822(91)90787-c.

Abstract

The structural genes of the prohead of phage phi 29 of Bacillus subtilis and a small phi 29 RNA (sRNA) were cloned and expressed in Escherichia coli individually or in combination to study the role of the sRNA in prohead assembly and the mechanism of prohead morphogenesis. The genes coding for the proteins of the scaffold (gp7), the capsid (gp8), the portal vertex (gp10), and the dispensable head fiber (gp8.5) were expressed in E. coli and the gene products were assembled, with and without the presence of the sRNA, into uniform and prolate particles that resembled the typical native phi 29 prohead. No differences in particle size and shape were found between the particles of 7-8-8.5-10 (scaffold-capsid-fiber-portal vertex) and 7-8-8.5-10-RNA (scaffold-capsid-fiber-portal vertex-RNA), suggesting that the phi 29 sRNA was not required for phi 29 prohead assembly. The 7-8-8.5-10 particles produced in E. coli in the absence of phi 29 sRNA were fully competent to package phi 29 DNA in the defined in vitro DNA packaging system by the addition of purified sRNA. Moreover, these DNA-filled heads were assembled into infectious virions in extracts. Without the addition of the sRNA, the 7-8-8.5-10 particles were incompetent while the 7-8-8.5-10-RNA particles were competent in DNA packaging. Bacterial sRNA present in E. coli cannot substitute for the phi 29 sRNA. The assembly of prohead particles in E. coli indicated that host factors unique to B. subtilis were not required. The evidence that the phi 29 sRNA was not required for phi 29 prohead assembly and was not a fixed structural component of the phi 29 prohead favors the conclusion that the phi 29 sRNA is a specific enzyme or morphogenetic factor in DNA packaging.

摘要

克隆了枯草芽孢杆菌噬菌体phi 29前头部的结构基因和一种小的phi 29 RNA(sRNA),并分别或联合在大肠杆菌中进行表达,以研究sRNA在前头部组装中的作用以及前头部形态发生的机制。编码支架蛋白(gp7)、衣壳蛋白(gp8)、门户顶点蛋白(gp10)和可有可无的头部纤维蛋白(gp8.5)的基因在大肠杆菌中表达,并且在有或没有sRNA存在的情况下,基因产物组装成了类似于典型天然phi 29前头部的均匀且呈长形的颗粒。在7-8-8.5-10(支架-衣壳-纤维-门户顶点)颗粒和7-8-8.5-10-RNA(支架-衣壳-纤维-门户顶点-RNA)颗粒之间未发现颗粒大小和形状的差异,这表明phi 29前头部组装不需要phi 29 sRNA。在没有phi 29 sRNA的情况下在大肠杆菌中产生的7-8-8.5-10颗粒,通过添加纯化的sRNA,在确定的体外DNA包装系统中完全能够包装phi 29 DNA。此外,这些充满DNA的头部在提取物中组装成了有感染性的病毒粒子。如果不添加sRNA,7-8-8.5-10颗粒无包装能力,而7-8-8.5-10-RNA颗粒具有DNA包装能力。大肠杆菌中存在的细菌sRNA不能替代phi 29 sRNA。在大肠杆菌中前头部颗粒的组装表明不需要枯草芽孢杆菌特有的宿主因子。phi 29前头部组装不需要phi 29 sRNA且它不是phi 29前头部的固定结构成分这一证据支持了phi 29 sRNA是DNA包装中的一种特异性酶或形态发生因子这一结论。

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