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U1小核核糖核蛋白在剪接体组装早期是必需的。

U1 small nuclear ribonucleoproteins are required early during spliceosome assembly.

作者信息

Zillmann M, Rose S D, Berget S M

机构信息

Verna and Marrs McLean Department of Biochemistry, Baylor College and Medicine, Houston, Texas 77030.

出版信息

Mol Cell Biol. 1987 Aug;7(8):2877-83. doi: 10.1128/mcb.7.8.2877-2883.1987.

DOI:10.1128/mcb.7.8.2877-2883.1987
PMID:2959853
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC367906/
Abstract

U1 small nuclear ribonucleoproteins (snRNPs) are required for in vitro splicing of pre-mRNA. Sequences within U1 RNA hybridize to, and thus recognize, 5' splice junctions. We have investigated the mechanism of association of U1 snRNPs with the spliceosome. U1-specific antibodies detected U1 association with precursor RNA early during assembly. Removal of the 5' terminal sequences of U1 RNA by oligo-directed cleavage or removal of U1 snRNPs by immunoprecipitation prior to the addition of precursor RNA depressed the association of all snRNPs with precursor RNA as detected by immunoprecipitation of splicing complexes by either Sm or U1-specific antibodies. Assembly of the spliceosome as monitored by gel electrophoresis was also depressed after cleavage of U1 RNA. The dependency of Sm precipitability of precursor RNA upon the presence of U1 snRNPs suggests that U1 snRNPs participate in the early recognition of substrate RNAs by U2 to U6 snRNPs. Although removal of the 5'-terminal sequences of U1 depressed U1 snRNP association with precursor RNA, it did not eliminate it, suggesting semistable association of U1 snRNPs with the assembling spliceosome in the absence of U1 RNA hybridization. This association was not dependent upon 5' splice junction sequences but was dependent upon 3' intronic sequences, indicating that U1 snRNPs interact with factors recognizing 3' intronic sequences. Mutual dependence of 5' and 3' recognition factors suggests significant snRNP-snRNP communication during early assembly.

摘要

U1小核核糖核蛋白(snRNP)是前体mRNA体外剪接所必需的。U1 RNA中的序列与5'剪接位点杂交,从而识别该位点。我们研究了U1 snRNP与剪接体结合的机制。U1特异性抗体在组装早期检测到U1与前体RNA结合。在添加前体RNA之前,通过寡核苷酸定向切割去除U1 RNA的5'末端序列或通过免疫沉淀去除U1 snRNP,会降低所有snRNP与前体RNA的结合,这可通过Sm或U1特异性抗体对剪接复合物进行免疫沉淀来检测。在切割U1 RNA后,通过凝胶电泳监测的剪接体组装也受到抑制。前体RNA的Sm可沉淀性对U1 snRNP存在的依赖性表明,U1 snRNP参与了U2至U6 snRNP对底物RNA的早期识别。虽然去除U1的5'末端序列会降低U1 snRNP与前体RNA的结合,但并未消除这种结合,这表明在没有U1 RNA杂交的情况下,U1 snRNP与正在组装的剪接体存在半稳定结合。这种结合不依赖于5'剪接位点序列,而是依赖于3'内含子序列,表明U1 snRNP与识别3'内含子序列的因子相互作用。5'和3'识别因子的相互依赖性表明在早期组装过程中snRNP之间存在重要的通讯。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3f3/367906/8530a56c5965/molcellb00080-0239-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3f3/367906/f7148aab3f99/molcellb00080-0237-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3f3/367906/b9e21f24c652/molcellb00080-0237-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3f3/367906/19293772f335/molcellb00080-0237-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3f3/367906/a7162c0478c8/molcellb00080-0238-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3f3/367906/6a7a0ddc76e8/molcellb00080-0239-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3f3/367906/8530a56c5965/molcellb00080-0239-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3f3/367906/f7148aab3f99/molcellb00080-0237-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3f3/367906/b9e21f24c652/molcellb00080-0237-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3f3/367906/19293772f335/molcellb00080-0237-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3f3/367906/a7162c0478c8/molcellb00080-0238-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3f3/367906/6a7a0ddc76e8/molcellb00080-0239-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3f3/367906/8530a56c5965/molcellb00080-0239-b.jpg

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U1 small nuclear ribonucleoproteins are required early during spliceosome assembly.U1小核核糖核蛋白在剪接体组装早期是必需的。
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本文引用的文献

1
The 5' terminus of the RNA moiety of U1 small nuclear ribonucleoprotein particles is required for the splicing of messenger RNA precursors.U1小核核糖核蛋白颗粒的RNA部分的5'末端是信使RNA前体剪接所必需的。
Cell. 1984 Aug;38(1):299-307. doi: 10.1016/0092-8674(84)90551-8.
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Lariat RNA's as intermediates and products in the splicing of messenger RNA precursors.套索RNA作为信使RNA前体剪接过程中的中间体和产物。
Science. 1984 Aug 31;225(4665):898-903. doi: 10.1126/science.6206566.
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The U1 small nuclear RNA-protein complex selectively binds a 5' splice site in vitro.
从大肠杆菌中纯化 SRSF1 用于生物物理和生物化学分析。
Curr Protoc. 2024 Apr;4(4):e1017. doi: 10.1002/cpz1.1017.
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Stoichiometries of U2AF35, U2AF65 and U2 snRNP reveal new early spliceosome assembly pathways.U2AF35、U2AF65和U2 snRNP的化学计量揭示了新的早期剪接体组装途径。
Nucleic Acids Res. 2017 Feb 28;45(4):2051-2067. doi: 10.1093/nar/gkw860.
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Splicing of internal large exons is defined by novel cis-acting sequence elements.内部大外显子的剪接由新的顺式作用序列元件定义。
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Regulation of mammalian spliceosome assembly by a protein phosphorylation mechanism.通过蛋白质磷酸化机制对哺乳动物剪接体组装的调控。
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Mol Cell Biol. 1995 Nov;15(11):6377-85. doi: 10.1128/MCB.15.11.6377.
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Proc Natl Acad Sci U S A. 1986 Feb;83(4):887-91. doi: 10.1073/pnas.83.4.887.