• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

I组C类核酶的P5激活剂可替代I组A类核酶的P7.1/7.2激活剂。

The P5 activator of a group IC ribozyme can replace the P7.1/7.2 activator of a group IA ribozyme.

作者信息

Ikawa Yoshiya, Sasaki Kenta, Tominaga Hiroyuki, Inoue Tan

机构信息

Graduate School of Biostudies, Kyoto University, Kyoto 606-8502, Japan.

出版信息

J Biochem. 2003 May;133(5):665-70. doi: 10.1093/jb/mvg085.

DOI:10.1093/jb/mvg085
PMID:12801919
Abstract

The P5 or P7 extensions in the group I intron ribozyme serve as "modular activator units" by stabilizing the conserved core of the ribozyme. The P5 extension of a group IC1 intron was introduced to a barely active group IA2 intron lacking its original P7 extension. The inserted P5 extension significantly activated the chimeric construct. Because the CYT-18 protein factor is also known to activate mutant group IA2 and IC1 introns lacking their P7 and P5 extensions, respectively, the RNA and protein activator units function in an analogous manner.

摘要

I组内含子核酶中的P5或P7延伸序列通过稳定核酶的保守核心,作为“模块化激活单元”发挥作用。将I C1组内含子的P5延伸序列引入到一个几乎没有活性、缺乏其原始P7延伸序列的I A2组内含子中。插入的P5延伸序列显著激活了嵌合构建体。由于已知CYT-18蛋白因子也分别激活缺乏其P7和P5延伸序列的I A2组和I C1组突变内含子,因此RNA和蛋白质激活单元以类似的方式发挥作用。

相似文献

1
The P5 activator of a group IC ribozyme can replace the P7.1/7.2 activator of a group IA ribozyme.I组C类核酶的P5激活剂可替代I组A类核酶的P7.1/7.2激活剂。
J Biochem. 2003 May;133(5):665-70. doi: 10.1093/jb/mvg085.
2
Installation of orthogonality to the interface that assembles two modular domains in the Tetrahymena group I ribozyme.正交安装到接口上,组装四膜虫组 I 核酶的两个模块域。
J Biosci Bioeng. 2014 Apr;117(4):407-12. doi: 10.1016/j.jbiosc.2013.10.008. Epub 2013 Nov 8.
3
Self-splicing of the Tetrahymena group I ribozyme without conserved base-triples.嗜热四膜虫I组核酶在没有保守碱基三联体情况下的自我剪接
Genes Cells. 2001 May;6(5):411-20. doi: 10.1046/j.1365-2443.2001.00437.x.
4
Role of a conserved J8/7 X P4 base-triple in the Tetrahymena ribozyme.保守的J8/7×P4碱基三联体在嗜热四膜虫核酶中的作用。
J Biochem. 2002 Nov;132(5):713-8. doi: 10.1093/oxfordjournals.jbchem.a003278.
5
A chemical phylogeny of group I introns based upon interference mapping of a bacterial ribozyme.基于细菌核酶干涉图谱的I类内含子化学系统发育学。
J Mol Biol. 2000 Sep 15;302(2):339-58. doi: 10.1006/jmbi.2000.4056.
6
Trans-activation of the Tetrahymena ribozyme by its P2-2.1 domains.四膜虫核酶通过其P2-2.1结构域的反式激活。
J Biochem. 1998 Mar;123(3):528-33. doi: 10.1093/oxfordjournals.jbchem.a021968.
7
Analysis of the P7 region within the catalytic core of the Tetrahymena ribozyme by employing in vitro selection.通过体外筛选对嗜热四膜虫核酶催化核心内的P7区域进行分析。
Nucleic Acids Symp Ser. 2000(44):197-8. doi: 10.1093/nass/44.1.197.
8
Concerted effects of two activator modules on the group I ribozyme reaction.两个激活模块对I组核酶反应的协同作用。
J Biochem. 2009 Apr;145(4):429-35. doi: 10.1093/jb/mvn183. Epub 2009 Jan 3.
9
Conserved base-pairings between C266-A268 and U307-G309 in the P7 of the Tetrahymena ribozyme is nonessential for the in vitro self-splicing reaction.嗜热四膜虫核酶P7区域中C266 - A268与U307 - G309之间保守的碱基配对对于体外自我剪接反应并非必需。
Biochem Biophys Res Commun. 2001 Jun 22;284(4):948-54. doi: 10.1006/bbrc.2001.5072.
10
Identification of the nucleotides in the A-rich bulge of the Tetrahymena ribozyme responsible for an efficient self-splicing reaction.
J Biochem. 1997 Oct;122(4):878-82. doi: 10.1093/oxfordjournals.jbchem.a021836.

引用本文的文献

1
A kinetic and thermodynamic framework for the Azoarcus group I ribozyme reaction.嗜氮根瘤菌属I类核酶反应的动力学和热力学框架。
RNA. 2014 Nov;20(11):1732-46. doi: 10.1261/rna.044362.114. Epub 2014 Sep 22.
2
Rational optimization of the DSL ligase ribozyme with GNRA/receptor interacting modules.使用GNRA/受体相互作用模块对DSL连接酶核酶进行合理优化。
Arch Biochem Biophys. 2009 Oct 15;490(2):163-70. doi: 10.1016/j.abb.2009.08.020. Epub 2009 Sep 1.