RNA-RNA interaction and gene splicing.

Cancer biochemistry biophysics Pub Date : 1997-06-01
M Verma, R N Kurl, C Blass, E A Davidson
{"title":"RNA-RNA interaction and gene splicing.","authors":"M Verma,&nbsp;R N Kurl,&nbsp;C Blass,&nbsp;E A Davidson","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The precise excision of intervening sequences during RNA splicing is an interesting example of the high degree of specificity involved in biosynthesis processes. Self-splicing RNA precursors achieve this specificity primarily through intramolecular interactions whereas all other types of RNA splicing requires interaction between cellular factors and specific recognition signals in the RNA precursor. About twelve years ago, the in vitro splicing system was developed and a general scheme of the pre-mRNA was proposed (Hernandez and Keller, 1983; Krainer et al., 1984; Lin et al., 1985; Padgett et al., 1984; Ruskin et al., 1984). A fundamental question in the splicing field is how the 5' and 3' splice sites are recognized and paired during the splicing reaction. Recent work in the splicing field has established that a network of RNA interactions may form the structural foundation of the spliceosomes. Possible solutions to many unsolved puzzles are getting attention. RNA-RNA interactions now appear to underlie many aspects of substrate recognition, reaction partner juxtaposition and catalysis. In this article we have presented the latest mechanisms involved in the pre-mRNA splicing and their implication in applied research including cancer.</p>","PeriodicalId":9552,"journal":{"name":"Cancer biochemistry biophysics","volume":"15 4","pages":"211-20"},"PeriodicalIF":0.0000,"publicationDate":"1997-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer biochemistry biophysics","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The precise excision of intervening sequences during RNA splicing is an interesting example of the high degree of specificity involved in biosynthesis processes. Self-splicing RNA precursors achieve this specificity primarily through intramolecular interactions whereas all other types of RNA splicing requires interaction between cellular factors and specific recognition signals in the RNA precursor. About twelve years ago, the in vitro splicing system was developed and a general scheme of the pre-mRNA was proposed (Hernandez and Keller, 1983; Krainer et al., 1984; Lin et al., 1985; Padgett et al., 1984; Ruskin et al., 1984). A fundamental question in the splicing field is how the 5' and 3' splice sites are recognized and paired during the splicing reaction. Recent work in the splicing field has established that a network of RNA interactions may form the structural foundation of the spliceosomes. Possible solutions to many unsolved puzzles are getting attention. RNA-RNA interactions now appear to underlie many aspects of substrate recognition, reaction partner juxtaposition and catalysis. In this article we have presented the latest mechanisms involved in the pre-mRNA splicing and their implication in applied research including cancer.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
RNA-RNA相互作用和基因剪接。
在RNA剪接过程中,精确切除介入序列是生物合成过程中高度特异性的一个有趣例子。自剪接RNA前体主要通过分子内相互作用实现这种特异性,而所有其他类型的RNA剪接都需要细胞因子和RNA前体中特定识别信号之间的相互作用。大约12年前,体外剪接系统被开发出来,并提出了pre-mRNA的一般方案(Hernandez and Keller, 1983;Krainer et al., 1984;Lin et al., 1985;Padgett et al., 1984;Ruskin et al., 1984)。剪接领域的一个基本问题是如何在剪接反应中识别和配对5'和3'剪接位点。最近在剪接领域的工作已经确定,RNA相互作用的网络可能形成剪接体的结构基础。许多尚未解决的谜题的可能解决方案正在引起人们的注意。RNA-RNA相互作用现在似乎是底物识别,反应伙伴并置和催化的许多方面的基础。在本文中,我们介绍了mrna前剪接的最新机制及其在包括癌症在内的应用研究中的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Lactoferrin expression in human breast cancer. Modulation of the impaired drug metabolism in sarcoma-180-bearing mice by echitamine chloride. Magnetic field induced inhibition of human osteosarcoma cells treated with adriamycin. Modulating effect of new potential antimelanomic agents, spin-labeled triazenes and nitrosoureas on the DOPA-oxidase activity of tyrosinase. Molecular basis of specific inhibition of urokinase plasminogen activator by amiloride.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1