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PMID: 12114529 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Predictive identification of exonic splicing enhancers in human genes.

Science (New York, N.Y.) ·Vol. 297 ·No. 5583 ·2002-08-09 ·Pages 1007-13

Fairbrother WG, Yeh RF, Sharp PA, Burge CB

Abstract

Specific short oligonucleotide sequences that enhance pre-mRNA splicing when present in exons, termed exonic splicing enhancers (ESEs), play important roles in constitutive and alternative splicing. A computational method, RESCUE-ESE, was developed that predicts which sequences have ESE activity by statistical analysis of exon-intron and splice site composition. When large data sets of human gene sequences were used, this method identified 10 predicted ESE motifs. Representatives of all 10 motifs were found to display enhancer activity in vivo, whereas point mutants of these sequences exhibited sharply reduced activity. The motifs identified enable prediction of the splicing phenotypes of exonic mutations in human genes.

MeSH Terms
Computational Biology Consensus Sequence DNA, Complementary Databases, Nucleic Acid Exons Genes Genome, Human Humans Hypoxanthine Phosphoribosyltransferase/genetics Introns Oligonucleotides/genetics Point Mutation RNA Splicing Regulatory Sequences, Nucleic Acid Sequence Analysis, DNA
Chemicals
DNA, Complementary Oligonucleotides Hypoxanthine Phosphoribosyltransferase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Fairbrother William G
Department of Biology, Center for Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Yeh Ru-Fang
Sharp Phillip A
Burge Christopher B
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
1095-9203
Published
2002-08-09
Epub
2002-00-11
Pages
1007-13
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NHGRI NIH HHS · 1 R01 HG02439-01 · United States
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