首页> 外文OA文献 >Bacteriophage T4-induced anticodon-loop nuclease detected in a host strain restrictive to RNA ligase mutants.
【2h】

Bacteriophage T4-induced anticodon-loop nuclease detected in a host strain restrictive to RNA ligase mutants.

机译:在限制RNA连接酶突变的宿主菌株中检测到噬菌体T4诱导的反密码子环核酸酶。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The fate of host tRNAs during T4 bacteriophage infection was investigated with Escherichia coli CTr5x, the only known host strain that is restrictive to RNA ligase and polynucleotide kinase mutants. Three CTr5x tRNA species were cleaved during infection. One was leucine tRNA1, which was cleaved in the extra arm, as reported elsewhere for E. coli B infected with bacteriophage T2 or T4. The other two were specific to E. coli CTr5x and were not cleaved in various other hosts. One of the cleaved CTr5x-specific tRNAs had an anticodon sequence of the E. coli B "major" isoleucine tRNA but otherwise little sequence homology. Both CTr5x-specific tRNAs were cleaved by a distinct T4-induced endonuclease, other than that of leucine tRNA1, because the CTr5x-specific cleavages (i) were induced later in infection, (ii) persisted with a T4 mutant deficient in leucine tRNA1 endonuclease, and (iii) occurred in the anticodon loop. The specific manifestation of the anticodon-directed endonuclease activity in T4-infected E. coli CTr5x suggests roles for RNA ligase and polynucleotide kinase in processing of host tRNA species.
机译:用大肠杆菌CTr5x研究了T4噬菌体感染期间宿主tRNA的命运,这是唯一已知的限制RNA连接酶和多核苷酸激酶突变体的宿主菌株。感染期间切割了三个CTr5x tRNA物种。一种是亮氨酸tRNA1,其在额外的臂中被切割,如其他地方报道的感染了噬菌体T2或T4的大肠杆菌B。另外两个是对大肠杆菌CTr5x特异的,未在其他各种宿主中裂解。切割的CTr5x特异性tRNA之一具有大肠杆菌B“主要”异亮氨酸tRNA的反密码子序列,但序列同源性很小。两种CTr5x特异性tRNA均被亮氨酸tRNA1以外的独特的T4诱导的核酸内切酶裂解,因为CTr5x特异性裂解(i)在感染后期被诱导,(ii)持续存在亮氨酸tRNA1核酸内切酶缺陷的T4突变体。 (iii)出现在反密码子环中。在T4感染的大肠杆菌CTr5x中,反密码子指导的核酸内切酶活性的特定表现表明RNA连接酶和多核苷酸激酶在宿主tRNA物种加工中的作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号