• 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

Two conserved structural components, A-rich bulge and P4 XJ6/7 base-triples, in activating the group I ribozymes.

作者信息

Ikawa Yoshiya, Yoshimura Takeshi, Hara Hidemi, Shiraishi Hideaki, Inoue Tan

机构信息

Graduate School of Biostudies, Kyoto University, Japan.

出版信息

Genes Cells. 2002 Dec;7(12):1205-15. doi: 10.1046/j.1365-2443.2002.00601.x.

DOI:10.1046/j.1365-2443.2002.00601.x
PMID:12485161
Abstract

BACKGROUND

The A-rich bulge of the group I intron ribozyme, a highly conserved structural element in its P5 peripheral region, plays a significant role in activating the ribozyme. The bulge has been known to interact with the P4 stem forming P4 XJ6/7 base-triples in the conserved core. The base-triples by themselves have also been identified as a distinctive element responsible for enhancing the activity of the ribozyme.

RESULTS

A weakly active variant of the Tetrahymena ribozyme lacking the P5 extension was dramatically activated by the addition of an A-rich bulge at the peripheral region, or by replacement of the original P4 XJ6/7 base-triples in the core structure with more stabilized isosteric ones. Biochemical analyses showed that the two methods of activation affect the ribozyme differently.

CONCLUSIONS

The long-range interaction between the A-rich bulge and P4 or additionally stabilized P4 XJ6/7 base-triples can contribute dramatically to activation of the Tetrahymena ribozyme. Both improve the kcat value, which represents the rate of the limiting step of the ribozyme reaction when its binding site is saturated with GTP. However, the bulge or the modified base-triples gave a moderate reduction or considerable increase, respectively, to the Km(GTP) value.

摘要

相似文献

1
Two conserved structural components, A-rich bulge and P4 XJ6/7 base-triples, in activating the group I ribozymes.
Genes Cells. 2002 Dec;7(12):1205-15. doi: 10.1046/j.1365-2443.2002.00601.x.
2
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.
3
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.
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
The P5abc peripheral element facilitates preorganization of the tetrahymena group I ribozyme for catalysis.P5abc外周元件促进嗜热四膜虫I组核酶的预组装以进行催化。
Biochemistry. 2000 Mar 14;39(10):2639-51. doi: 10.1021/bi992313g.
6
Mutations at the guanosine-binding site of the Tetrahymena ribozyme also affect site-specific hydrolysis.嗜热四膜虫核酶鸟苷结合位点的突变也会影响位点特异性水解。
Nucleic Acids Res. 1992 Dec 25;20(24):6613-9. doi: 10.1093/nar/20.24.6613.
7
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.
8
Minimal catalytic domain of a group I self-splicing intron RNA.第一类自我剪接内含子RNA的最小催化结构域。
Nat Struct Biol. 2000 Nov;7(11):1032-5. doi: 10.1038/80947.
9
RNA substrate binding site in the catalytic core of the Tetrahymena ribozyme.嗜热四膜虫核酶催化核心中的RNA底物结合位点。
Nature. 1992 Jul 9;358(6382):123-8. doi: 10.1038/358123a0.
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
A Phylogenetic Approach to Structural Variation in Organization of Nuclear Group I Introns and Their Ribozymes.一种研究核I组内含子及其核酶结构变异的系统发育方法。
Noncoding RNA. 2021 Jul 22;7(3):43. doi: 10.3390/ncrna7030043.
2
Cryo-EM structures of full-length Tetrahymena ribozyme at 3.1 Å resolution.全长四膜虫核酶的 3.1Å 分辨率冷冻电镜结构。
Nature. 2021 Aug;596(7873):603-607. doi: 10.1038/s41586-021-03803-w. Epub 2021 Aug 11.
3
Oligomerization of a Bimolecular Ribozyme Modestly Rescues its Structural Defects that Disturb Interdomain Assembly to Form the Catalytic Site.
双分子核酶的寡聚化适度挽救了其结构缺陷,这些缺陷干扰了结构域间的组装以形成催化位点。
J Mol Evol. 2018 Aug;86(7):431-442. doi: 10.1007/s00239-018-9862-8. Epub 2018 Aug 14.
4
Use of a Fluorescent Aptamer RNA as an Exonic Sequence to Analyze Self-Splicing Ability of aGroup I Intron from Structured RNAs.使用荧光适配体RNA作为外显子序列来分析来自结构化RNA的I组内含子的自我剪接能力。
Biology (Basel). 2016 Nov 17;5(4):43. doi: 10.3390/biology5040043.
5
Exploiting post-transcriptional regulation to probe RNA structures in vivo via fluorescence.利用转录后调控通过荧光在体内探测RNA结构。
Nucleic Acids Res. 2015 Jan;43(2):e13. doi: 10.1093/nar/gku1191. Epub 2014 Nov 21.
6
Structure-function analysis from the outside in: long-range tertiary contacts in RNA exhibit distinct catalytic roles.从外向内的结构功能分析:RNA 中的长程三级接触具有明显的催化作用。
Biochemistry. 2011 Oct 11;50(40):8733-55. doi: 10.1021/bi2008245. Epub 2011 Sep 19.
7
Long-term evolution of the S788 fungal nuclear small subunit rRNA group I introns.S788真菌核小亚基rRNA第一组内含子的长期进化
RNA. 2004 Jul;10(7):1084-96. doi: 10.1261/rna.5202704.
8
Putative intermediary stages for the molecular evolution from a ribozyme to a catalytic RNP.从核酶到催化性核糖核蛋白分子进化的假定中间阶段。
Nucleic Acids Res. 2003 Mar 1;31(5):1488-96. doi: 10.1093/nar/gkg225.