Evidence map›Paper›PMID 20019791›Full record

ArticlePLoS computational biology2009

Predicting functional alternative splicing by measuring RNA selection pressure from multigenome alignments.

Hongchao Lu, Lan Lin, Seiko Sato, Yi Xing, Christopher J Lee

Abstract read
In one paragraph

Article in PLoS computational biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

  1. Src dependency of the regulation of LTP by alternative splicing ofPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. PDZD7 and hearing loss: More than just a modifier.American journal of medical genetics. Part A · 2015
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. The function of introns.Frontiers in genetics · 2012
    Article
  15. Article
  16. Article
  17. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Hongchao LuMolecular Biology Institute, Center for Computational Biology, Institute for Genomics and Proteomics, Department of Chemistry and Biochemistry, University of California Los Angeles, Los Angeles, California, USA.
Lan Lin
Seiko Sato
Yi Xing
Christopher J Lee

Funding

Center for Computational Biology (RMI)U54RR021813 · NCRR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TOGA, ARTHUR W · 2004 to 2010
$25.3M
Statistical Analysis of Exon ArraysR01HG004634 · NHGRI · STANFORD UNIVERSITY · PI WONG, WING H. · 2008 to 2011
$1.4M
NCRR NIH HHS U54 RR021813NHGRI NIH HHS 1R01HG004634NHGRI NIH HHS R01 HG004634
6 · The paper itself

Abstract

High-throughput methods such as EST sequencing, microarrays and deep sequencing have identified large numbers of alternative splicing (AS) events, but studies have shown that only a subset of these may be functional. Here we report a sensitive bioinformatics approach that identifies exons with evidence of a strong RNA selection pressure ratio (RSPR)--i.e., evolutionary selection against mutations that change only the mRNA sequence while leaving the protein sequence unchanged--measured across an entire evolutionary family, which greatly amplifies its predictive power. Using the UCSC 28 vertebrate genome alignment, this approach correctly predicted half to three-quarters of AS exons that are known binding targets of the NOVA splicing regulatory factor, and predicted 345 strongly selected alternative splicing events in human, and 262 in mouse. These predictions were strongly validated by several experimental criteria of functional AS such as independent detection of the same AS event in other species, reading frame-preservation, and experimental evidence of tissue-specific regulation: 75% (15/20) of a sample of high-RSPR exons displayed tissue specific regulation in a panel of ten tissues, vs. only 20% (4/20) among a sample of low-RSPR exons. These data suggest that RSPR can identify exons with functionally important splicing regulation, and provides biologists with a dataset of over 600 such exons. We present several case studies, including both well-studied examples (GRIN1) and novel examples (EXOC7). These data also show that RSPR strongly outperforms other approaches such as standard sequence conservation (which fails to distinguish amino acid selection pressure from RNA selection pressure), or pairwise genome comparison (which lacks adequate statistical power for predicting individual exons).

Indexed as

Alternative SplicingModels, GeneticAnimalsCarrier ProteinsComputational BiologyExpressed Sequence TagsGenomeHumansMiceNerve Tissue ProteinsOligonucleotide Array Sequence AnalysisReceptors, N-Methyl-D-AspartateReproducibility of ResultsReverse Transcriptase Polymerase Chain ReactionRNASequence AlignmentCarrier ProteinsExoc7 protein, mouseGprin1 protein, mouseGRIN1 protein, humanNerve Tissue ProteinsReceptors, N-Methyl-D-AspartateRNAVesicular Transport Proteins

Identifiers

PMID20019791
PMCPMC2784930

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.