4.8 Article

Distribution of SR protein exonic splicing enhancer motifs in human protein-coding genes

期刊

NUCLEIC ACIDS RESEARCH
卷 33, 期 16, 页码 5053-5062

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OXFORD UNIV PRESS
DOI: 10.1093/nar/gki810

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资金

  1. NCI NIH HHS [R33 CA088351, CA88351, R21 CA088351] Funding Source: Medline
  2. NHGRI NIH HHS [HG01696, R01 HG001696] Funding Source: Medline
  3. NIGMS NIH HHS [R37 GM042699, GM42699, R01 GM042699] Funding Source: Medline
  4. NATIONAL CANCER INSTITUTE [R33CA088351, R21CA088351] Funding Source: NIH RePORTER
  5. NATIONAL HUMAN GENOME RESEARCH INSTITUTE [R01HG001696] Funding Source: NIH RePORTER
  6. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM042699] Funding Source: NIH RePORTER

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Exonic splicing enhancers (ESEs) are pre-mRNA cis-acting elements required for splice-site recognition. We previously developed a web-based program called ESEfinder that scores any sequence for the presence of ESE motifs recognized by the human SR proteins SF2/ASF, SRp40, SRp55 and SC35 (http://rulai.cshl.edu/tools/ESE/). Using ESEfinder, we have undertaken a large-scale analysis of ESE motif distribution in human protein-coding genes. Significantly higher frequencies of ESE motifs were observed in constitutive internal protein-coding exons, compared with both their flanking intronic regions and with pseudo exons. Statistical analysis of ESE motif frequency distributions revealed a complex relationship between splice-site strength and increased or decreased frequencies of particular SR protein motifs. Comparison of constitutively and alternatively spliced exons demonstrated slightly weaker splice-site scores, as well as significantly fewer ESE motifs, in the alternatively spliced group. Our results underline the importance of ESE-mediated SR protein function in the process of exon definition, in the context of both constitutive splicing and regulated alternative splicing.

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