首页> 外文期刊>Biochimie >EFFECT OF MODIFIED NUCLEOTIDES ON STRUCTURE OF YEAST TRNA(PHE) - COMPARATIVE STUDIES BY METAL ION-INDUCED HYDROLYSIS AND NUCLEASE MAPPING
【24h】

EFFECT OF MODIFIED NUCLEOTIDES ON STRUCTURE OF YEAST TRNA(PHE) - COMPARATIVE STUDIES BY METAL ION-INDUCED HYDROLYSIS AND NUCLEASE MAPPING

机译:修饰的核苷酸对酵母TRNA(PHE)结构的影响-金属离子水解和核酸酶作图的比较研究

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Structural differences between native yeast tRNA(Phe), its in vitro transcript and the U8G mutant have been investigated using metal ion-induced hydrolysis and nuclease digestion. Differences in the solution structure of the molecules involve four regions: the D- and T-loops, the variable region and the anticodon loop. Efficiency of the Pb(II); Eu(II)-, Mn(II)- and Mg(II)-induced hydrolysis at the main cleavage sites in the D-loop is significantly reduced for unmodified tRNAs. Moreover, only the in vitro transcripts are susceptible for cleavage in the T-loop and entire anticodon loop. Other changes in the transcript molecule involve 50-fold enhancement of S-1 nuclease digestion at p36, weak cleavages in the D-loop and lack of some digestion sites in the T-loop. The nuclease V-1 digestion patterns are very similar for studied molecules. Changes in the pattern of hydrolysis of the D-loop caused by mutation of the conservative base U8 to G are detected by metal-induced hydrolysis only. Our results indicate clearly that metal ions acid enzymatic probes monitor different features of RNA structure and their combined use is highly advantageous in studying subtle structural changes in tRNA. [References: 39]
机译:使用金属离子诱导的水解和核酸酶消化研究了天然酵母tRNA(Phe),其体外转录本和U8G突变体之间的结构差异。分子溶液结构的差异涉及四个区域:D环和T环,可变区和反密码子环。铅(II)的效率;对于未修饰的tRNA,E-(II)-,Mn(II)-和Mg(II)诱导的D环主要切割位点的水解显着降低。而且,仅体外转录物在T-环和整个反密码子环中易切割。转录物分子中的其他变化包括p36处S-1核酸酶消化增强了50倍,D环中的弱切割和T环中缺少一些消化位点。核酸酶V-1的消化模式与研究分子非常相似。仅由金属诱导的水解可以检测到由保守碱基U8突变为G引起的D环水解模式的变化。我们的结果清楚地表明,金属离子酸酶探针可监测RNA结构的不同特征,并且它们的组合使用在研究tRNA的细微结构变化方面非常有利。 [参考:39]

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