...
首页> 外文期刊>Nucleic Acids Research >ENZYMATIC SYNTHESIS OF 2'-MODIFIED NUCLEIC ACIDS - IDENTIFICATION OF IMPORTANT PHOSPHATE AND RIBOSE MOIETIES IN RNASE P SUBSTRATES
【24h】

ENZYMATIC SYNTHESIS OF 2'-MODIFIED NUCLEIC ACIDS - IDENTIFICATION OF IMPORTANT PHOSPHATE AND RIBOSE MOIETIES IN RNASE P SUBSTRATES

机译:酶法合成2'修饰的核酸-鉴定RNASE P基质中重要的磷酸盐和核糖部分

获取原文
获取原文并翻译 | 示例
           

摘要

For the first time mosaic nucleic acids composed of 50% RNA and 50% DNA can be obtained as transcripts with T7 RNA polymerase. Two NTPs could be replaced simultaneously in a transcription reaction, This means more than 40 deoxynucleotides were inserted in one transcript, Previously, a maximum of two deoxynucleotides could be incorporated and 2'-O-methyl-NTPs were not substrates at all, We obtained reasonable transcript yields with a maximal level of 99% 2'-O-methyl-NTPs, and the products contained up to 58% 2'-O-methylnucleotides at more than 20 positions, Sequence-specific nucleotide incorporation was monitored by sequence ladders (partial alkali or iodine cleavage), No base misincorporations were detected with 100% dGTP, dCTP and dTTP, and with partial incorporation of dATP alpha S, 2'-O-methyl-GTP alpha S and 2'-O-methyl-CTP alpha S, whereas they were found with dATP 2'-O-methyl-ATP alpha S and 2'-O-methyl-UTP alpha S. Quantitative data allow predetermined modification levels of partially modified transcripts, Highly modified transcripts can be used for structural and functional studies, in modification interference approaches and for in vitro evolution procedures. Modification interference studies revealed a small number of important phosphate and ribose moieties in RNase P substrates. The conversion of T7 RNA polymerase to a DNA polymerase extends the observation that there is no absolute distinction between RNA and DNA polymerases, Accordingly, an adapted concept of a primordial RNA world is presented.
机译:首次可以用T7 RNA聚合酶获得由50%RNA和50%DNA组成的镶嵌核酸。在转录反应中可以同时替换两个NTP,这意味着一个转录物中插入了40多个脱氧核苷酸,以前最多可以掺入两个脱氧核苷酸,而2'-O-甲基-NTP根本不是底物,我们获得了合理的转录本产量,最高水平为99%2'-O-甲基-NTPs,并且产物在20多个位置上包含高达58%的2'-O-甲基核苷酸,通过序列阶梯监控序列特异性核苷酸的掺入(部分碱或碘裂解),未检测到100%dGTP,dCTP和dTTP以及部分dATP alpha S,2'-O-甲基-GTP alpha S和2'-O-甲基-CTP alpha碱基错掺S,而它们具有dATP 2'-O-甲基-ATP alpha S和2'-O-甲基-UTP alphaS。定量数据可对部分修饰的转录本进行预定的修饰,而高度修饰的转录本可用于结构修饰和功能研究,修改int参考方法和体外进化程序。修饰干扰研究表明,RNase P底物中有少量重要的磷酸和核糖部分。 T7 RNA聚合酶向DNA聚合酶的转化扩展了观察到RNA与DNA聚合酶之间没有绝对区别的观点。因此,提出了原始RNA世界的一种适用概念。

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