• 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

Mechanism of 3' splice site selection by the catalytic core of the sunY intron of bacteriophage T4: the role of a novel base-pairing interaction in group I introns.

作者信息

Michel F, Netter P, Xu M Q, Shub D A

机构信息

Centre de Génétique Moléculaire du Centre National de la Recherche Scientifique, Université Pierre et Marie Curie, Gif-sur-Yvette, France.

出版信息

Genes Dev. 1990 May;4(5):777-88. doi: 10.1101/gad.4.5.777.

DOI:10.1101/gad.4.5.777
PMID:2379829
Abstract

The catalytic core of the sunY intron of bacteriophage T4 is separated from its 3' exon by 837 nucleotides, most of which are part of an open reading frame (ORF). Here, we report that transcripts truncated within the sunY ORF self-splice in vitro to a variety of sites in the segment immediately 3' of the core. Recognition of these proximal splice sites is shown to depend on (1) the presence on the intron side of a terminal G, which must not be part of a secondary structure; and (2) the ability of the penultimate intron nucleotide to base-pair with a 3' splice site-binding sequence (3'SSBS) located within the core. The counterpart of the 3'SSBS can be identified in most group I introns. The possible significance of such alternative splicing events for in vivo expression of intron-encoded proteins is discussed.

摘要

相似文献

1
Mechanism of 3' splice site selection by the catalytic core of the sunY intron of bacteriophage T4: the role of a novel base-pairing interaction in group I introns.
Genes Dev. 1990 May;4(5):777-88. doi: 10.1101/gad.4.5.777.
2
The catalytic core of the sunY intron of bacteriophage T4.噬菌体T4的sunY内含子的催化核心。
Gene. 1989 Oct 15;82(1):77-82. doi: 10.1016/0378-1119(89)90032-2.
3
Activation of the catalytic core of a group I intron by a remote 3' splice junction.I类内含子催化核心被远端3'剪接位点激活。
Genes Dev. 1992 Aug;6(8):1373-85. doi: 10.1101/gad.6.8.1373.
4
Monitoring of the cooperative unfolding of the sunY group I intron of bacteriophage T4. The active form of the sunY ribozyme is stabilized by multiple interactions with 3' terminal intron components.噬菌体T4的sunY I组内含子协同解折叠的监测。sunY核酶的活性形式通过与3'末端内含子组分的多重相互作用得以稳定。
J Mol Biol. 1993 Nov 20;234(2):331-46. doi: 10.1006/jmbi.1993.1590.
5
Spontaneous shuffling of domains between introns of phage T4.噬菌体T4内含子之间结构域的自发重排。
Nature. 1990 Jul 26;346(6282):394-6. doi: 10.1038/346394a0.
6
The inconsistent distribution of introns in the T-even phages indicates recent genetic exchanges.T偶数噬菌体中内含子分布的不一致表明了近期的基因交换。
Nucleic Acids Res. 1989 Jan 11;17(1):301-15. doi: 10.1093/nar/17.1.301.
7
Miniribozymes, small derivatives of the sunY intron, are catalytically active.微小核酶是sunY内含子的小衍生物,具有催化活性。
Mol Cell Biol. 1989 Dec;9(12):5480-3. doi: 10.1128/mcb.9.12.5480-5483.1989.
8
Genes within genes: independent expression of phage T4 intron open reading frames and the genes in which they reside.基因中的基因:噬菌体T4内含子开放阅读框与其所在基因的独立表达。
Genes Dev. 1988 Dec;2(12B):1791-9. doi: 10.1101/gad.2.12b.1791.
9
Sequence specificity of the P6 pairing for splicing of the group I td intron of phage T4.噬菌体T4 I组td内含子剪接中P6配对的序列特异性
Nucleic Acids Res. 1989 Nov 25;17(22):9147-63. doi: 10.1093/nar/17.22.9147.
10
Functional and sequence analysis of splicing defective nrdB mutants of bacteriophage T4 reveal new bases and a new sub-domain required for group I intron self-splicing.噬菌体T4剪接缺陷型nrdB突变体的功能和序列分析揭示了I组内含子自我剪接所需的新碱基和新亚结构域。
Biochim Biophys Acta. 1997 Jan 3;1350(1):89-97. doi: 10.1016/s0167-4781(96)00151-0.

引用本文的文献

1
Efficient circularization of protein-encoding RNAs via a novel cis-splicing system.通过新型顺式剪接系统实现蛋白质编码 RNA 的高效环化。
Nucleic Acids Res. 2024 Sep 23;52(17):10400-10415. doi: 10.1093/nar/gkae711.
2
Snapshots of the second-step self-splicing of Tetrahymena ribozyme revealed by cryo-EM.低温电镜揭示四膜虫核酶两步自我剪接的瞬时结构。
Nat Commun. 2023 Mar 16;14(1):1294. doi: 10.1038/s41467-023-36724-5.
3
Crystal structure studies of RNA duplexes containing s(2)U:A and s(2)U:U base pairs.含硫代2'-尿苷:腺嘌呤和硫代2'-尿苷:尿嘧啶碱基对的RNA双链体的晶体结构研究
J Am Chem Soc. 2014 Oct 1;136(39):13916-24. doi: 10.1021/ja508015a. Epub 2014 Sep 16.
4
Structural insights of non-canonical U*U pair and Hoogsteen interaction probed with Se atom.利用硒原子探测非规范 U*U 对和 Hoogsteen 相互作用的结构见解。
Nucleic Acids Res. 2013 Dec;41(22):10476-87. doi: 10.1093/nar/gkt799. Epub 2013 Sep 5.
5
Yeast transcripts cleaved by an internal ribozyme provide new insight into the role of the cap and poly(A) tail in translation and mRNA decay.被内部核酶切割的酵母转录本为帽结构和聚腺苷酸尾在翻译和mRNA降解中的作用提供了新的见解。
RNA. 2006 Jul;12(7):1323-37. doi: 10.1261/rna.46306. Epub 2006 May 19.
6
A small insertion in the SSU rDNA of the lichen fungus Arthonia lapidicola is a degenerate group-I intron.地衣真菌石生节盘衣(Arthonia lapidicola)的小亚基核糖体DNA(SSU rDNA)中的一个小插入片段是一个简并的I类内含子。
Curr Genet. 1996 May;29(6):582-6. doi: 10.1007/BF02426963.
7
An RNA fragment consisting of the P7 and P9.0 stems and the 3'-terminal guanosine of the Tetrahymena group I intron.一个由嗜热四膜虫I组内含子的P7和P9.0茎以及3'末端鸟苷组成的RNA片段。
Nucleic Acids Res. 1996 Apr 1;24(7):1337-44. doi: 10.1093/nar/24.7.1337.
8
Interlocked circle formation by group I introns: structural requirements and mechanism.I类内含子的连锁环形成:结构要求和机制
Nucleic Acids Res. 1993 Jul 11;21(14):3217-26. doi: 10.1093/nar/21.14.3217.
9
Methylation interference experiments identify bases that are essential for distinct catalytic functions of a group I ribozyme.甲基化干扰实验确定了对于I组核酶不同催化功能至关重要的碱基。
EMBO J. 1993 Dec;12(12):4747-54. doi: 10.1002/j.1460-2075.1993.tb06163.x.
10
The in vivo use of alternate 3'-splice sites in group I introns.I组内含子中交替3'剪接位点的体内应用。
Nucleic Acids Res. 1994 Apr 11;22(7):1135-7. doi: 10.1093/nar/22.7.1135.