Evidence map›Paper›PMID 16709259›Full record

ArticleBMC bioinformatics2006

The effects of multiple features of alternatively spliced exons on the K(A)/K(S) ratio test.

Feng-Chi Chen, Trees-Juen Chuang

Abstract readComparative Study
In one paragraph

Article in BMC bioinformatics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Position-dependent correlations between DNA methylation and the evolutionary rates of mammalian coding exons.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  3. Article
  4. Article
  5. Article
4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Feng-Chi ChenGenomics Research Center, Academia Sinica, Academia Road, Nankang, Taipei 11529, Taiwan. fcchen@iis.sinica.edu.tw
Trees-Juen Chuang

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe evolution of alternatively spliced exons (ASEs) is of primary interest because these exons are suggested to be a major source of functional diversity of proteins. Many exon features have been suggested to affect the evolution of ASEs. However, previous studies have relied on the KA/KS ratio test without taking into consideration information sufficiency (i.e., exon length > 75 bp, cross-species divergence > 5%) of the studied exons, leading to potentially biased interpretations. Furthermore, which exon feature dominates the results of the KA/KS ratio test and whether multiple exon features have additive effects have remained unexplored.

resultsIn this study, we collect two different datasets for analysis - the ASE dataset (which includes lineage-specific ASEs and conserved ASEs) and the ACE dataset (which includes only conserved ASEs). We first show that information sufficiency can significantly affect the interpretation of relationship between exons features and the KA/KS ratio test results. After discarding exons with insufficient information, we use a Boolean method to analyze the relationship between test results and four exon features (namely length, protein domain overlapping, inclusion level, and exonic splicing enhancer (ESE) frequency) for the ASE dataset. We demonstrate that length and protein domain overlapping are dominant factors, and they have similar impacts on test results of ASEs. In addition, despite the weak impacts of inclusion level and ESE motif frequency when considered individually, combination of these two factors still have minor additive effects on test results. However, the ACE dataset shows a slightly different result in that inclusion level has a marginally significant effect on test results. Lineage-specific ASEs may have contributed to the difference. Overall, in both ASEs and ACEs, protein domain overlapping is the most dominant exon feature while ESE frequency is the weakest one in affecting test results.

conclusionThe proposed method can easily find additive effects of individual or multiple factors on the KA/KS ratio test results of exons. Therefore, the system can analyze complex conditions in evolution where multiple features are involved. More factors can also be added into the system to extend the scope of evolutionary analysis of exons. In addition, our method may be useful when orthologous exons can not be found for the KA/KS ratio test.

Indexed as

Alternative SplicingEvolution, MolecularAnimalsBase SequenceConserved SequenceDatabases, GeneticEnhancer Elements, GeneticExonsHumansMiceModels, GeneticProteinsProtein Structure, TertiaryRNA, MessengerRNA Splice SitesSequence AlignmentProteinsRNA, MessengerRNA Splice Sites

Identifiers

PMID16709259
PMCPMC1526763

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.