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Sequence requirements in different steps of the pre-mRNA splicing reaction: analysis by the RNA modification-exclusion technique.

作者信息

Lang K M, Keller W

机构信息

Department of Cell Biology, Biocenter of the University of Basel, Switzerland.

出版信息

Mol Cell Biol. 1990 Sep;10(9):4942-7. doi: 10.1128/mcb.10.9.4942-4947.1990.

DOI:10.1128/mcb.10.9.4942-4947.1990
PMID:2201909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC361115/
Abstract

The stepwise assembly of splicing complexes and the subsequent splicing reaction were analyzed by the RNA modification-exclusion technique, which generates the equivalent of a complete set of point mutations in a single reaction. We found that although the sequences surrounding the 5' splice site, the branch point, and the 3' splice site, including the 3' AG, were required for presplicing complex formation, modified nucleotides at these positions were not completely excluded. The same sequences were required for splicing complex formation; however, modified nucleotides in these sequences were excluded to a much greater extent.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c65e/361115/204c4259ace5/molcellb00045-0516-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c65e/361115/204c4259ace5/molcellb00045-0516-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c65e/361115/204c4259ace5/molcellb00045-0516-a.jpg

相似文献

1
Sequence requirements in different steps of the pre-mRNA splicing reaction: analysis by the RNA modification-exclusion technique.
Mol Cell Biol. 1990 Sep;10(9):4942-7. doi: 10.1128/mcb.10.9.4942-4947.1990.
2
Effect of 5' splice site mutations on splicing of the preceding intron.5'剪接位点突变对前一个内含子剪接的影响。
Mol Cell Biol. 1990 Dec;10(12):6299-305. doi: 10.1128/mcb.10.12.6299-6305.1990.
3
The organization of 3' splice-site sequences in mammalian introns.哺乳动物内含子中3'剪接位点序列的组织方式。
Genes Dev. 1989 Dec;3(12B):2113-23. doi: 10.1101/gad.3.12b.2113.
4
Analysis of RNase-A-resistant regions of adenovirus 2 major late precursor-mRNA in splicing extracts reveals an ordered interaction of nuclear components with the substrate RNA.在剪接提取物中对腺病毒2型主要晚期前体mRNA的核糖核酸酶A抗性区域进行分析,揭示了核成分与底物RNA之间的有序相互作用。
J Mol Biol. 1987 Aug 5;196(3):559-73. doi: 10.1016/0022-2836(87)90032-5.
5
Stepwise assembly of a pre-mRNA splicing complex requires U-snRNPs and specific intron sequences.前体mRNA剪接复合体的逐步组装需要U型小核核糖核蛋白颗粒(U-snRNPs)和特定的内含子序列。
Cell. 1985 Aug;42(1):355-67. doi: 10.1016/s0092-8674(85)80131-8.
6
Measurement and analysis of yeast pre-mRNA sequence contribution to splicing efficiency.
Methods Enzymol. 1990;181:122-47. doi: 10.1016/0076-6879(90)81116-c.
7
A chemical modification/interference study of yeast pre-mRNA spliceosome assembly and splicing.酵母前体信使核糖核酸剪接体组装与剪接的化学修饰/干扰研究
Genes Dev. 1988 Apr;2(4):428-39. doi: 10.1101/gad.2.4.428.
8
Yeast pre-mRNA splicing requires a minimum distance between the 5' splice site and the internal branch acceptor site.酵母前体mRNA剪接需要5'剪接位点与内部分支受体位点之间有最小距离。
Mol Cell Biol. 1987 Nov;7(11):4010-6. doi: 10.1128/mcb.7.11.4010-4016.1987.
9
A mutational analysis of the polypyrimidine tract of introns. Effects of sequence differences in pyrimidine tracts on splicing.内含子多嘧啶序列的突变分析。嘧啶序列差异对剪接的影响。
J Biol Chem. 1993 May 25;268(15):11222-9.
10
Polyoma virus small tumor antigen pre-mRNA splicing requires cooperation between two 3' splice sites.多瘤病毒小肿瘤抗原前体信使核糖核酸剪接需要两个3'剪接位点之间的协同作用。
Proc Natl Acad Sci U S A. 1990 May;87(9):3338-42. doi: 10.1073/pnas.87.9.3338.

引用本文的文献

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Characterization of human RNA splice signals by iterative functional selection of splice sites.通过剪接位点的迭代功能选择对人类RNA剪接信号进行表征。
RNA. 2000 Apr;6(4):528-44. doi: 10.1017/s1355838200992033.
2
Bimolecular exon ligation by the human spliceosome bypasses early 3' splice site AG recognition and requires NTP hydrolysis.人类剪接体介导的双分子外显子连接绕过早期3'剪接位点AG识别且需要NTP水解。
RNA. 2000 Jan;6(1):16-25. doi: 10.1017/s1355838200001862.
3
Modification interference approach to detect ribose moieties important for the optimal activity of a ribozyme.

本文引用的文献

1
Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei.从分离的哺乳动物细胞核的可溶性提取物中,RNA聚合酶II进行准确的转录起始。
Nucleic Acids Res. 1983 Mar 11;11(5):1475-89. doi: 10.1093/nar/11.5.1475.
2
Purification of a protein required for the splicing of pre-mRNA and its separation from the lariat debranching enzyme.前体信使核糖核酸剪接所需蛋白质的纯化及其与套索脱支酶的分离。
EMBO J. 1985 Dec 16;4(13A):3571-81. doi: 10.1002/j.1460-2075.1985.tb04119.x.
3
Role of the 3' splice site consensus sequence in mammalian pre-mRNA splicing.
用于检测对核酶最佳活性至关重要的核糖部分的修饰干扰方法。
Nucleic Acids Res. 1993 Jan 11;21(1):21-6. doi: 10.1093/nar/21.1.21.
4
Exon recognition and nucleocytoplasmic partitioning determine AMPD1 alternative transcript production.外显子识别和核质分配决定了AMPD1可变转录本的产生。
Mol Cell Biol. 1991 Oct;11(10):5356-63. doi: 10.1128/mcb.11.10.5356-5363.1991.
5
Cleavage and polyadenylation factor CPF specifically interacts with the pre-mRNA 3' processing signal AAUAAA.切割与聚腺苷酸化因子CPF特异性地与前体mRNA的3'加工信号AAUAAA相互作用。
EMBO J. 1991 Dec;10(13):4241-9. doi: 10.1002/j.1460-2075.1991.tb05002.x.
6
Phosphorothioate substitution identifies phosphate groups important for pre-mRNA splicing.硫代磷酸酯取代鉴定出对前体mRNA剪接重要的磷酸基团。
Nucleic Acids Res. 1992 Apr 25;20(8):1949-57. doi: 10.1093/nar/20.8.1949.
3'剪接位点共有序列在哺乳动物前体mRNA剪接中的作用。
Nature. 1985;317(6039):732-4. doi: 10.1038/317732a0.
4
The "spliceosome": yeast pre-messenger RNA associates with a 40S complex in a splicing-dependent reaction.“剪接体”:酵母前体信使核糖核酸在剪接依赖性反应中与一个40S复合体结合。
Science. 1985 May 24;228(4702):963-7. doi: 10.1126/science.3890181.
5
Intron sequences involved in lariat formation during pre-mRNA splicing.前体mRNA剪接过程中参与套索形成的内含子序列。
Cell. 1985 May;41(1):95-105. doi: 10.1016/0092-8674(85)90064-9.
6
Sequence requirements for splicing of higher eukaryotic nuclear pre-mRNA.高等真核生物细胞核前体mRNA剪接的序列要求。
Cell. 1986 Nov 21;47(4):555-65. doi: 10.1016/0092-8674(86)90620-3.
7
A compensatory base change in U1 snRNA suppresses a 5' splice site mutation.U1小核核糖核酸中的一种补偿性碱基变化抑制了5'剪接位点突变。
Cell. 1986 Sep 12;46(6):827-35. doi: 10.1016/0092-8674(86)90064-4.
8
Two spliceosomes can form simultaneously and independently on synthetic double-intron messenger RNA precursors.两个剪接体可以在合成的双内含子信使核糖核酸前体上同时且独立地形成。
EMBO J. 1987 Jun;6(6):1747-55. doi: 10.1002/j.1460-2075.1987.tb02427.x.
9
Effect of mutations at the lariat branch acceptor site on beta-globin pre-mRNA splicing in vitro.套索分支接受位点突变对β-珠蛋白前体mRNA体外剪接的影响。
Nature. 1986;324(6097):589-91. doi: 10.1038/324589a0.
10
Specific small nuclear RNAs are associated with yeast spliceosomes.特定的小核RNA与酵母剪接体相关。
Cell. 1986 Jun 20;45(6):869-77. doi: 10.1016/0092-8674(86)90561-1.