• 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

四膜虫核酶通过其P2-2.1结构域的反式激活。

Trans-activation of the Tetrahymena ribozyme by its P2-2.1 domains.

作者信息

Ikawa Y, Shiraishi H, Inoue T

机构信息

Department of Chemistry, Faculty of Science, Kyoto University, Sakyo-ku, Kyoto 606-01, Japan.

出版信息

J Biochem. 1998 Mar;123(3):528-33. doi: 10.1093/oxfordjournals.jbchem.a021968.

DOI:10.1093/oxfordjournals.jbchem.a021968
PMID:9538238
Abstract

The Tetrahymena group I self-splicing intron contains peripheral domains P2-2.1. Mutant introns lacking these domains are hardly active. We found that if an independently prepared P2-2.1 RNA is added in trans, it efficiently enhances the catalytic activity of an intron lacking the domains. P2-2.1 RNA together with the previously identified activator, P5abc RNA, of the Tetrahymena intron can activate the intron lacking both of them. The trans-activation depends on the long-range interaction between P2.1 and P9.1 domains.

摘要

嗜热四膜虫I组自剪接内含子包含外周结构域P2-2.1。缺少这些结构域的突变内含子几乎没有活性。我们发现,如果以反式添加独立制备的P2-2.1 RNA,它能有效增强缺少这些结构域的内含子的催化活性。P2-2.1 RNA与先前鉴定出的嗜热四膜虫内含子激活剂P5abc RNA一起,可以激活同时缺少这两者的内含子。反式激活取决于P2.1和P9.1结构域之间的长程相互作用。

相似文献

1
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.
2
Trans-activation of the Tetrahymena group I intron ribozyme via a non-native RNA-RNA interaction.通过非天然RNA-RNA相互作用对嗜热四膜虫I组内含子核酶进行反式激活。
Nucleic Acids Res. 1999 Apr 1;27(7):1650-5. doi: 10.1093/nar/27.7.1650.
3
P5abc of the Tetrahymena ribozyme consists of three functionally independent elements.四膜虫核酶的P5abc由三个功能独立的元件组成。
RNA. 1998 Jul;4(7):837-46. doi: 10.1017/s1355838298972016.
4
Characterization of the newly constructed domains that replace P5abc within the Tetrahymena ribozyme.对四膜虫核酶内取代P5abc的新构建结构域的表征。
FEBS Lett. 1996 Sep 23;394(1):5-8. doi: 10.1016/0014-5793(96)00918-0.
5
Requirements for alternative forms of the activator domain, P5abc, in the Tetrahymena ribozyme.嗜热四膜虫核酶中激活结构域P5abc替代形式的要求
FEBS Lett. 2000 Jan 28;466(2-3):273-8. doi: 10.1016/s0014-5793(99)01797-4.
6
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.
7
Long-range interaction between the P2.1 and P9.1 peripheral domains of the Tetrahymena ribozyme.嗜热四膜虫核酶P2.1和P9.1外周结构域之间的长程相互作用。
Nucleic Acids Res. 1997 May 1;25(9):1761-5. doi: 10.1093/nar/25.9.1761.
8
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.
9
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.
10
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.

引用本文的文献

1
Rational Design of an Orthogonal Pair of Bimolecular RNase P Ribozymes through Heterologous Assembly of Their Modular Domains.通过模块化结构域的异源组装对双分子RNase P核酶的正交对进行合理设计。
Biology (Basel). 2019 Aug 31;8(3):65. doi: 10.3390/biology8030065.
2
A two-piece derivative of a group I intron RNA as a platform for designing self-assembling RNA templates to promote Peptide ligation.I组内含子RNA的一种两件式衍生物,作为设计自组装RNA模板以促进肽连接的平台。
J Nucleic Acids. 2012;2012:305867. doi: 10.1155/2012/305867. Epub 2012 Aug 22.
3
A peripheral element assembles the compact core structure essential for group I intron self-splicing.
一个外围元件组装了I组内含子自我剪接所必需的紧密核心结构。
Nucleic Acids Res. 2005 Aug 12;33(14):4602-11. doi: 10.1093/nar/gki770. Print 2005.