• 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

前体信使核糖核酸剪接过程中的初始剪接位点识别与配对。

Initial splice-site recognition and pairing during pre-mRNA splicing.

作者信息

Reed R

机构信息

Department of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Curr Opin Genet Dev. 1996 Apr;6(2):215-20. doi: 10.1016/s0959-437x(96)80053-0.

DOI:10.1016/s0959-437x(96)80053-0
PMID:8722179
Abstract

Advances over the past year have provided new insights into the mechanisms involved in the initial recognition and pairing of the 5' and 3' splice sites in complex metazoan pre-mRNAs. Highlights include the demonstration that exonic enhancers can promote trans splicing and that an excess of the serine and arginine rich family of splicing proteins can obviate the requirement for U1 small nuclear ribonucleoprotein particle in splicing.

摘要

过去一年的研究进展为深入了解复杂后生动物前体mRNA中5'和3'剪接位点的初始识别和配对机制提供了新的见解。其中的亮点包括:证明外显子增强子可促进反式剪接,以及富含丝氨酸和精氨酸的剪接蛋白家族过量时可消除剪接过程中对U1小核核糖核蛋白颗粒的需求。

相似文献

1
Initial splice-site recognition and pairing during pre-mRNA splicing.前体信使核糖核酸剪接过程中的初始剪接位点识别与配对。
Curr Opin Genet Dev. 1996 Apr;6(2):215-20. doi: 10.1016/s0959-437x(96)80053-0.
2
Factors involved in the activation of pre-mRNA splicing from downstream splicing enhancers.参与从下游剪接增强子激活前体mRNA剪接的因素。
J Biochem. 1996 Jul;120(1):53-60. doi: 10.1093/oxfordjournals.jbchem.a021393.
3
SR proteins promote the first specific recognition of Pre-mRNA and are present together with the U1 small nuclear ribonucleoprotein particle in a general splicing enhancer complex.SR蛋白促进对前体信使核糖核酸(Pre-mRNA)的首次特异性识别,并与U1小核核糖核蛋白颗粒一起存在于一个通用剪接增强子复合体中。
Mol Cell Biol. 1994 Nov;14(11):7670-82. doi: 10.1128/mcb.14.11.7670-7682.1994.
4
A two-step mechanism for 5' and 3' splice-site pairing.5'和3'剪接位点配对的两步机制。
Nature. 1995 Jun 8;375(6531):510-3. doi: 10.1038/375510a0.
5
Purine-rich enhancers function in the AT-AC pre-mRNA splicing pathway and do so independently of intact U1 snRNP.富含嘌呤的增强子在AT-AC前体mRNA剪接途径中发挥作用,且其作用独立于完整的U1 snRNP。
RNA. 1998 Dec;4(12):1664-73. doi: 10.1017/s1355838298981432.
6
Deletion of the N-terminus of SF2/ASF permits RS-domain-independent pre-mRNA splicing.删除 SF2/ASF 的 N 端允许 RS 结构域独立的前体 mRNA 剪接。
PLoS One. 2007 Sep 5;2(9):e854. doi: 10.1371/journal.pone.0000854.
7
Pre-mRNA splicing of IgM exons M1 and M2 is directed by a juxtaposed splicing enhancer and inhibitor.免疫球蛋白M(IgM)外显子M1和M2的前体信使核糖核酸(pre-mRNA)剪接受并列的剪接增强子和抑制剂指导。
Genes Dev. 1999 Feb 15;13(4):462-71. doi: 10.1101/gad.13.4.462.
8
Mechanism for cryptic splice site activation during pre-mRNA splicing.前体mRNA剪接过程中隐蔽剪接位点激活的机制。
Proc Natl Acad Sci U S A. 1990 Aug;87(16):6253-7. doi: 10.1073/pnas.87.16.6253.
9
Pre-mRNA splicing in the absence of an SR protein RS domain.缺乏SR蛋白RS结构域时的前体mRNA剪接
Genes Dev. 2000 Dec 15;14(24):3166-78. doi: 10.1101/gad.189500.
10
A downstream splicing enhancer is essential for in vitro pre-mRNA splicing.下游剪接增强子对体外前体mRNA剪接至关重要。
FEBS Lett. 1999 May 14;451(1):10-4. doi: 10.1016/s0014-5793(99)00521-9.

引用本文的文献

1
DHX9 helicase impacts on splicing decisions by modulating U2 snRNP recruitment in Ewing sarcoma cells.DHX9解旋酶通过调节尤因肉瘤细胞中U2小核核糖核蛋白的募集来影响剪接决定。
Nucleic Acids Res. 2025 Feb 8;53(4). doi: 10.1093/nar/gkaf068.
2
Structural insights into the cross-exon to cross-intron spliceosome switch.结构洞察跨外显子到跨内含子剪接体开关。
Nature. 2024 Jun;630(8018):1012-1019. doi: 10.1038/s41586-024-07458-1. Epub 2024 May 22.
3
Loss-of-function mutation in PRMT9 causes abnormal synapse development by dysregulation of RNA alternative splicing.
PRMT9 功能丧失性突变通过调控 RNA 可变剪接导致异常突触发育。
Nat Commun. 2024 Apr 1;15(1):2809. doi: 10.1038/s41467-024-47107-9.
4
Somatic Mutations in Core Spliceosome Components Promote Tumorigenesis and Generate an Exploitable Vulnerability in Human Cancer.核心剪接体成分中的体细胞突变促进肿瘤发生并在人类癌症中产生可利用的脆弱性。
Cancers (Basel). 2022 Apr 4;14(7):1827. doi: 10.3390/cancers14071827.
5
Splicing efficiency of minor introns in a mouse model of SMA predominantly depends on their branchpoint sequence and can involve the contribution of major spliceosome components.在 SMA 的小鼠模型中,次要内含子的剪接效率主要取决于其分支点序列,并可能涉及主要剪接体成分的贡献。
RNA. 2022 Mar;28(3):303-319. doi: 10.1261/rna.078329.120. Epub 2021 Dec 10.
6
Evolution of the Early Spliceosomal Complex-From Constitutive to Regulated Splicing.早期剪接体复合物的演变——从组成型剪接至调控性剪接。
Int J Mol Sci. 2021 Nov 18;22(22):12444. doi: 10.3390/ijms222212444.
7
An Exon Skipping in Is Associated with Perturbed Chloroplast Development in Maize.外显子跳跃与玉米叶绿体发育异常有关。
Int J Mol Sci. 2021 Oct 1;22(19):10668. doi: 10.3390/ijms221910668.
8
Splice and Dice: Intronic microRNAs, Splicing and Cancer.剪接与切割:内含子微小RNA、剪接与癌症
Biomedicines. 2021 Sep 19;9(9):1268. doi: 10.3390/biomedicines9091268.
9
Expression of a human cDNA in moss results in spliced mRNAs and fragmentary protein isoforms.人类cDNA在苔藓中的表达产生了剪接的mRNA和片段化的蛋白质异构体。
Commun Biol. 2021 Aug 12;4(1):964. doi: 10.1038/s42003-021-02486-3.
10
At the Intersection of Major and Minor Spliceosomes: Crosstalk Mechanisms and Their Impact on Gene Expression.在主要和次要剪接体的交汇处:相互作用机制及其对基因表达的影响。
Front Genet. 2021 Jul 20;12:700744. doi: 10.3389/fgene.2021.700744. eCollection 2021.