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Measurement and analysis of yeast pre-mRNA sequence contribution to splicing efficiency.

作者信息

Rymond B C, Pikielny C, Seraphin B, Legrain P, Rosbash M

出版信息

Methods Enzymol. 1990;181:122-47. doi: 10.1016/0076-6879(90)81116-c.

DOI:10.1016/0076-6879(90)81116-c
PMID:2116568
Abstract
摘要

相似文献

1
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.
2
Exon mutations uncouple 5' splice site selection from U1 snRNA pairing.外显子突变使5'剪接位点选择与U1 snRNA配对解偶联。
Cell. 1990 Nov 2;63(3):619-29. doi: 10.1016/0092-8674(90)90457-p.
3
A non-conserved sequence in the 5'region of the CYH2 intron from Saccharomyces cerevisiae controls splicing efficiency of the pre-mRNA.来自酿酒酵母的CYH2内含子5'区域的一个非保守序列控制着前体mRNA的剪接效率。
Yeast. 1988 Sep;4(3):209-17. doi: 10.1002/yea.320040306.
4
Evidence for an essential non-Watson-Crick interaction between the first and last nucleotides of a nuclear pre-mRNA intron.核前体mRNA内含子第一个和最后一个核苷酸之间存在关键的非沃森-克里克相互作用的证据。
Nature. 1993 Feb 18;361(6413):660-2. doi: 10.1038/361660a0.
5
Some cis- and trans-acting mutants for splicing target pre-mRNA to the cytoplasm.
Cell. 1989 May 19;57(4):573-83. doi: 10.1016/0092-8674(89)90127-x.
6
Size and position of intervening sequences are critical for the splicing efficiency of pre-mRNA in the yeast Saccharomyces cerevisiae.间隔序列的大小和位置对于酿酒酵母中前体mRNA的剪接效率至关重要。
Nucleic Acids Res. 1985 Jun 11;13(11):3791-804. doi: 10.1093/nar/13.11.3791.
7
Yeast pre-messenger RNA splicing efficiency depends on critical spacing requirements between the branch point and 3' splice site.酵母前体信使核糖核酸剪接效率取决于分支点与3'剪接位点之间的关键间距要求。
EMBO J. 1986 May;5(5):1023-30. doi: 10.1002/j.1460-2075.1986.tb04317.x.
8
Cooperative interaction of branch signals in the actin intron of Saccharomyces cerevisiae.酿酒酵母肌动蛋白内含子中分支信号的协同相互作用。
Nucleic Acids Res. 1998 Sep 15;26(18):4137-45. doi: 10.1093/nar/26.18.4137.
9
Nuclear pre-mRNA splicing in Saccharomyces cerevisiae.酿酒酵母中的核前体mRNA剪接
Biochem Soc Symp. 1989;55:69-75.
10
Impairment of yeast pre-mRNA splicing by potential secondary structure-forming sequences near the conserved branchpoint sequence.保守分支点序列附近潜在的二级结构形成序列对酵母前体mRNA剪接的损害。
Nucleic Acids Res. 1988 Nov 25;16(22):10413-23. doi: 10.1093/nar/16.22.10413.

引用本文的文献

1
Coupling of spliceosome complexity to intron diversity.剪接体复杂性与内含子多样性的偶联。
Curr Biol. 2021 Nov 22;31(22):4898-4910.e4. doi: 10.1016/j.cub.2021.09.004. Epub 2021 Sep 22.
2
Rds3p is required for stable U2 snRNP recruitment to the splicing apparatus.Rds3p是稳定招募U2 snRNP至剪接装置所必需的。
Mol Cell Biol. 2003 Oct;23(20):7339-49. doi: 10.1128/MCB.23.20.7339-7349.2003.
3
Genetic interactions with CLF1 identify additional pre-mRNA splicing factors and a link between activators of yeast vesicular transport and splicing.
与CLF1的遗传相互作用鉴定出了其他前体mRNA剪接因子以及酵母囊泡运输激活因子与剪接之间的联系。
Genetics. 2003 Jul;164(3):895-907. doi: 10.1093/genetics/164.3.895.
4
Generation of temperature-sensitive cbp1 strains of Saccharomyces cerevisiae by PCR mutagenesis and in vivo recombination: characteristics of the mutant strains imply that CBP1 is involved in stabilization and processing of cytochrome b pre-mRNA.通过PCR诱变和体内重组产生酿酒酵母温度敏感型cbp1菌株：突变菌株的特征表明CBP1参与细胞色素b前体mRNA的稳定和加工。
Genetics. 1993 Dec;135(4):981-91. doi: 10.1093/genetics/135.4.981.
5
Protein splicing removes intervening sequences in an archaea DNA polymerase.
Nucleic Acids Res. 1992 Dec 11;20(23):6153-7. doi: 10.1093/nar/20.23.6153.
6
TFC3: gene encoding the B-block binding subunit of the yeast transcription factor IIIC.TFC3：编码酵母转录因子IIIC的β-块结合亚基的基因。
Proc Natl Acad Sci U S A. 1992 Nov 1;89(21):10512-6. doi: 10.1073/pnas.89.21.10512.