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细胞类型特异性剪接因子与可变RNA剪接的调控

Cell-type-specific splicing factors and the regulation of alternative RNA splicing.

作者信息

Latchman D S

机构信息

Department of Biochemistry, University College and Middlesex School of Medicine, London.

出版信息

New Biol. 1990 Apr;2(4):297-303.

PMID:2126955
Abstract

A very wide variety of biological processes are regulated by alternative splicing. By this means, a gene can be transcribed in several different tissues but in each tissue the RNA transcript is spliced in a particular way to produce a different mRNA and hence a different protein. It is now clear that alternative splicing is regulated by factors which are expressed in a tissue-specific manner and which are necessary for the splicing events to occur. This review will discuss the evidence for the existence of these factors, their nature, and the mechanisms by which they regulate splicing by interacting with sequences in the RNA.

摘要

多种生物学过程受可变剪接调控。通过这种方式,一个基因可在几种不同组织中进行转录,但在每个组织中,RNA转录本以特定方式进行剪接,从而产生不同的mRNA,进而产生不同的蛋白质。现在已经清楚,可变剪接受以组织特异性方式表达的因子调控,这些因子是剪接事件发生所必需的。本综述将讨论这些因子存在的证据、它们的性质,以及它们通过与RNA中的序列相互作用来调控剪接的机制。

相似文献

1
Cell-type-specific splicing factors and the regulation of alternative RNA splicing.细胞类型特异性剪接因子与可变RNA剪接的调控
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2
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Essential nucleotides direct neuron-specific splicing of gamma 2 pre-mRNA.必需核苷酸指导γ2前体mRNA的神经元特异性剪接。
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Developmental and muscle-specific regulation of avian fast skeletal troponin T isoform expression by mRNA splicing.通过mRNA剪接对禽类快速骨骼肌肌钙蛋白T同工型表达进行发育和肌肉特异性调控。
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Broad specificity of SR (serine/arginine) proteins in the regulation of alternative splicing of pre-messenger RNA.SR(丝氨酸/精氨酸)蛋白在调控信使前体RNA可变剪接中的广泛特异性。
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Alternative production of calcitonin and CGRP mRNA is regulated at the calcitonin-specific splice acceptor.降钙素和降钙素基因相关肽信使核糖核酸的交替产生在降钙素特异性剪接受体处受到调控。
Nature. 1989 Sep 7;341(6237):76-80. doi: 10.1038/341076a0.
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引用本文的文献

1
Alternative splicing of the latency-related transcript of bovine herpesvirus 1 yields RNAs containing unique open reading frames.牛疱疹病毒1型潜伏相关转录本的可变剪接产生含有独特开放阅读框的RNA。
J Virol. 1998 Sep;72(9):7294-301. doi: 10.1128/JVI.72.9.7294-7301.1998.
2
The blocks to human immunodeficiency virus type 1 Tat and Rev functions in mouse cell lines are independent.人免疫缺陷病毒1型Tat和Rev功能在小鼠细胞系中的阻断作用是相互独立的。
J Virol. 1993 Apr;67(4):2349-54. doi: 10.1128/JVI.67.4.2349-2354.1993.
3
The snRNP core protein SmB and tissue-specific SmN protein are differentially distributed between snRNP particles.
小核核糖核蛋白(snRNP)核心蛋白SmB和组织特异性SmN蛋白在snRNP颗粒之间呈差异分布。
Nucleic Acids Res. 1993 Aug 25;21(17):4047-53. doi: 10.1093/nar/21.17.4047.
4
Distinct protein forms are produced from alternatively spliced bicistronic glutamic acid decarboxylase mRNAs during development.
Mol Cell Biol. 1994 Nov;14(11):7535-45. doi: 10.1128/mcb.14.11.7535-7545.1994.
5
Mice lacking Snrpn expression show normal regulation of neuronal alternative splicing events.
Mol Biol Rep. 1994 Jul;20(1):19-25. doi: 10.1007/BF00999851.
6
Differential expression of the mouse U1a and U1b SnRNA genes is not dependent on sequence differences in the octamer motif.小鼠U1a和U1b SnRNA基因的差异表达不依赖于八聚体基序中的序列差异。
Biochem J. 1991 Aug 1;277 ( Pt 3)(Pt 3):719-22. doi: 10.1042/bj2770719.
7
Isolation of hnRNP complexes from Drosophila melanogaster.从黑腹果蝇中分离异质核糖核蛋白复合物。
J Cell Biol. 1992 Jan;116(2):245-55. doi: 10.1083/jcb.116.2.245.
8
Gene regulation.
BMJ. 1992 Apr 25;304(6834):1103-5. doi: 10.1136/bmj.304.6834.1103.