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RNA介导的DNA包装入杂交λ/phi 29原头部的特异性。

RNA-mediated specificity of DNA packaging into hybrid lambda/phi 29 proheads.

作者信息

Valpuesta J M, Donate L E, Mier C, Herranz L, Carrascosa J L

机构信息

Centro de Biología Molecular Severo Ochoa (CSIC-UAM), Universidad Autónoma de Madrid, Spain.

出版信息

EMBO J. 1993 Nov;12(11):4453-9. doi: 10.1002/j.1460-2075.1993.tb06131.x.

Abstract

A small RNA (pRNA, 174 nt) is known to be essential for DNA packaging in bacteriophage phi 29. However, in an in vitro DNA packaging system based on hybrid lambda/phi 29 proheads (made up of head proteins from phage lambda and connectors from phage phi 29), the specificity of DNA packaging is lost, and different RNA molecules fulfil the requirements for DNA packaging, albeit with less efficiency than phi 29 pRNA. Competition assays with RNAs from different sources have shown that phi 29 connectors bind preferentially pRNA. An increase in the efficiency of phi 29 DNA packaging into hybrid proheads induced by phi 29 pRNA is observed because, when phi 29 pRNA is incubated with hybrid proheads, phi 29 DNA is packaged more efficiently than other DNAs of similar length. Furthermore, when hybrid proheads carrying phi 29 pRNA are incubated with a mixture of DNAs from different sources, phi 29 DNA is selectively packaged, thus indicating that phi 29 pRNA determines the specificity of DNA packaging.

摘要

已知一种小RNA(pRNA,174个核苷酸)对于噬菌体φ29的DNA包装至关重要。然而,在基于杂交λ/φ29原头部(由噬菌体λ的头部蛋白和噬菌体φ29的连接体组成)的体外DNA包装系统中,DNA包装的特异性丧失,不同的RNA分子满足DNA包装的要求,尽管效率低于φ29 pRNA。来自不同来源的RNA的竞争试验表明,φ29连接体优先结合pRNA。观察到由φ29 pRNA诱导的将φ29 DNA包装到杂交原头部中的效率增加,因为当φ29 pRNA与杂交原头部一起温育时,φ29 DNA比其他类似长度的DNA更有效地被包装。此外,当携带φ29 pRNA的杂交原头部与来自不同来源的DNA混合物一起温育时,φ29 DNA被选择性地包装,从而表明φ29 pRNA决定了DNA包装的特异性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ee7/413745/d5aa61516073/emboj00083-0411-a.jpg

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