Identification of Splicing Silencers and Enhancers in Sense Alu s: a Role for Pseudoacceptors in Splice Site Repression
Author:
Affiliation:
1. University of Southampton School of Medicine, Division of Human Genetics, Southampton SO16 6YD, United Kingdom
2. Karolinska Institute at NOVUM, Department of Biosciences, S-141 57 Huddinge, Sweden
Abstract
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Link
https://journals.asm.org/doi/pdf/10.1128/MCB.25.16.6912-6920.2005
Reference70 articles.
1. Arrisi-Mercado, P., M. Romano, A. F. Muro, and F. E. Baralle. 2004. An exonic splicing enhancer offsets the atypical GU-rich 3′ splice site of human apolipoprotein A-II exon 3. J. Biol. Chem. 279 : 39331-39339.
2. Batzer, M. A., and P. L. Deininger. 2002. Alu repeats and human genomic diversity. Nat. Rev. Genet. 3 : 370-379.
3. Berget, S. M. 1995. Exon recognition in vertebrate splicing. J. Biol. Chem. 270 : 2411-2414.
4. RNA Splicing at Human Immunodeficiency Virus Type 1 3′ Splice Site A2 Is Regulated by Binding of hnRNP A/B Proteins to an Exonic Splicing Silencer Element
5. Blanchette, M., and B. Chabot. 1999. Modulation of exon skipping by high-affinity hnRNP A1-binding sites and by intron elements that repress splice site utilization. EMBO J. 18 : 1939-1952.
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