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2
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3
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Optimal antisense target reducing INS intron 1 retention is adjacent to a parallel G quadruplex.减少胰岛素(INS)基因内含子1保留的最佳反义靶点与一个平行G-四链体相邻。
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本文引用的文献

1
Systematic identification and analysis of exonic splicing silencers.外显子剪接沉默子的系统鉴定与分析
Cell. 2004 Dec 17;119(6):831-45. doi: 10.1016/j.cell.2004.11.010.
2
Variation in sequence and organization of splicing regulatory elements in vertebrate genes.脊椎动物基因中剪接调控元件的序列和组织变异。
Proc Natl Acad Sci U S A. 2004 Nov 2;101(44):15700-5. doi: 10.1073/pnas.0404901101. Epub 2004 Oct 25.
3
Branch site haplotypes that control alternative splicing.控制可变剪接的分支位点单倍型。
Hum Mol Genet. 2004 Dec 15;13(24):3189-202. doi: 10.1093/hmg/ddh334. Epub 2004 Oct 20.
4
An exonic splicing enhancer offsets the atypical GU-rich 3' splice site of human apolipoprotein A-II exon 3.一个外显子剪接增强子可抵消人类载脂蛋白A-II外显子3非典型富含GU的3'剪接位点的影响。
J Biol Chem. 2004 Sep 17;279(38):39331-9. doi: 10.1074/jbc.M405566200. Epub 2004 Jul 7.
5
Computational definition of sequence motifs governing constitutive exon splicing.调控组成型外显子剪接的序列基序的计算定义
Genes Dev. 2004 Jun 1;18(11):1241-50. doi: 10.1101/gad.1195304. Epub 2004 May 14.
6
Minimal conditions for exonization of intronic sequences: 5' splice site formation in alu exons.内含子序列外显子化的最低条件:alu外显子中5'剪接位点的形成。
Mol Cell. 2004 Apr 23;14(2):221-31. doi: 10.1016/s1097-2765(04)00181-9.
7
Regulation of alternative RNA splicing by exon definition and exon sequences in viral and mammalian gene expression.病毒和哺乳动物基因表达中通过外显子定义和外显子序列对可变RNA剪接的调控。
J Biomed Sci. 2004 May-Jun;11(3):278-94. doi: 10.1007/BF02254432.
8
A variable dinucleotide repeat in the CFTR gene contributes to phenotype diversity by forming RNA secondary structures that alter splicing.囊性纤维化跨膜传导调节因子(CFTR)基因中的可变二核苷酸重复序列通过形成改变剪接的RNA二级结构,导致表型多样性。
Proc Natl Acad Sci U S A. 2004 Mar 9;101(10):3504-9. doi: 10.1073/pnas.0400182101. Epub 2004 Mar 1.
9
Analysis of a high-throughput yeast two-hybrid system and its use to predict the function of intracellular proteins encoded within the human MHC class III region.高通量酵母双杂交系统的分析及其在预测人类MHC III类区域编码的细胞内蛋白质功能中的应用。
Genomics. 2004 Jan;83(1):153-67. doi: 10.1016/s0888-7543(03)00235-0.
10
Two essential splice lariat branchpoint sequences in one intron in a xeroderma pigmentosum DNA repair gene: mutations result in reduced XPC mRNA levels that correlate with cancer risk.着色性干皮病DNA修复基因的一个内含子中有两个必需的剪接套索分支点序列:突变导致XPC mRNA水平降低,这与癌症风险相关。
Hum Mol Genet. 2004 Feb 1;13(3):343-52. doi: 10.1093/hmg/ddh026. Epub 2003 Dec 8.

有义Alu元件中剪接沉默子和增强子的鉴定:假受体在剪接位点抑制中的作用

Identification of splicing silencers and enhancers in sense Alus: a role for pseudoacceptors in splice site repression.

作者信息

Lei Haixin, Vorechovsky Igor

机构信息

University of Southampton School of Medicine, Division of Human Genetics, Duthie Building, UK.

出版信息

Mol Cell Biol. 2005 Aug;25(16):6912-20. doi: 10.1128/MCB.25.16.6912-6920.2005.

DOI:10.1128/MCB.25.16.6912-6920.2005
PMID:16055705
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1190243/
Abstract

Auxiliary splicing signals in introns play an important role in splice site selection, but these elements are poorly understood. We show that a subset of serine/arginine (SR)-rich proteins activate a cryptic 3' splice site in a sense Alu repeat located in intron 4 of the human LST1 gene. Utilization of this cryptic splice site is controlled by juxtaposed Alu-derived splicing silencers and enhancers between closely linked short tandem repeats TNFd and TNFe. Systematic mutagenesis of these elements showed that AG dinucleotides that were not preceded by purine residues were critical for repressing exon inclusion of a chimeric splicing reporter. Since the splice acceptor-like sequences are present in excess in exonic splicing silencers, these signals may contribute to inhibition of a large number of pseudosites in primate genomes.

摘要

内含子中的辅助剪接信号在剪接位点选择中起重要作用,但对这些元件的了解甚少。我们发现,富含丝氨酸/精氨酸(SR)的蛋白质子集激活了人类LST1基因第4内含子中一个有义Alu重复序列内的一个隐蔽3'剪接位点。该隐蔽剪接位点的利用受紧密连锁的短串联重复序列TNFd和TNFe之间并列的Alu衍生剪接沉默子和增强子控制。对这些元件的系统诱变表明,嘌呤残基之前不存在的AG二核苷酸对于抑制嵌合剪接报告基因的外显子包含至关重要。由于剪接受体样序列在外显子剪接沉默子中大量存在,这些信号可能有助于抑制灵长类基因组中的大量假位点。