...
首页> 外文期刊>Nucleic acids research >The environment of 5S rRNA in the ribosome: cross-links to 23S rRNA from sites within helices II and III of the 5S molecule
【24h】

The environment of 5S rRNA in the ribosome: cross-links to 23S rRNA from sites within helices II and III of the 5S molecule

机译:核糖体中5S rRNA的环境:从5S分子螺旋II和III内的位点与23S rRNA交联

获取原文
           

摘要

Three contiguous fragments of Escherichia coli 5S rRNA were prepared by T7 transcription from synthetic DNA templates. The central fragment, comprising residues 33–71 of the molecule, was transcribed in the presence of 4-thiouridine triphosphate together with [32P]UTP. The three transcripts were ligated together, yielding a 5S rRNA analogue carrying 4-thiouridine residues at positions 40, 48, 55 and 65 in helices II and III. After ligation, the 4-thiouridine residues were derivatised with p-azidophenacyl bromide. The modified 5S rRNA was reconstituted into 50S subunits and these subunits were used to prepare 70S ribosomes in the presence or absence of tRNA and mRNA. The azidophenyl groups were then photoactivated by mild irradiation at 300 nm and the products of cross-linking analysed by our standard procedures. Multiple crosslinks from 5S rRNA to two distinct regions of the 23S rRNA were observed. The first region was located in helix 38 in Domain II of the 23S molecule, with cross-links at sites between nucleotides 885 and 922. The second region covered helices 81–85 in Domain V, with sites between nucleotides 2272 and 2345. Taken together with previous data, these results serve to define the arrangement of the 5S rRNA molecule relative to the 23S rRNA within the 50S subunit.
机译:通过从合成DNA模板进行T7转录制备了大肠杆菌5S rRNA的三个连续片段。在4-硫尿苷三磷酸和[ 32 P] UTP的存在下转录包含该分子残基33-71的中央片段。将三个转录物连接在一起,产生在螺旋II和III中40、48、55和65位带有4-硫尿苷残基的5S rRNA类似物。连接后,将4-硫尿苷残基用对叠氮基苯甲酰溴衍生化。将修饰的5S rRNA重组为50S亚基,并在存在或不存在tRNA和mRNA的情况下,将这些亚基用于制备70S核糖体。然后通过在300 nm的温和照射将叠氮基苯基光活化,并通过我们的标准程序分析交联的产物。观察到从5S rRNA到23S rRNA两个不同区域的多重交联。第一个区域位于23S分子域II中的螺旋38中,在核苷酸885和922之间的位点具有交联。第二个区域覆盖域V中的螺旋81-85,位点在2272和2345核苷酸之间。与以前的数据一起,这些结果有助于确定5S rRNA分子相对于50S亚基中23S rRNA的排列。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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