Evidence map›Paper›PMID 20704715›Full record

ArticleGenome biology2010

Intronic motif pairs cooperate across exons to promote pre-mRNA splicing.

Shengdong Ke, Lawrence A Chasin

Open access · goldAbstract read
In one paragraph

Article in Genome biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.2field-weighted citation impact, top 21% of its field
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

22 citing papers in PubMed, 30 citations in OpenAlex.

  1. Single Antisense Oligonucleotides Correct Diverse Splicing Mutations in Hotspot Exons.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  2. Review
  3. Article
  4. Article
  5. Pseudoexons of the DMD Gene.Journal of neuromuscular diseases · 2020
    Review
  6. Review
  7. A birth of bipartite exon by intragenic deletion.Molecular genetics & genomic medicine · 2017
    Article
  8. Article
  9. Article
  10. Article
  11. Identifying splicing regulatory elements with de Bruijn graphs.Journal of computational biology : a journal of computational molecular cell biology · 2014
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

2 authors at 1 institution in 1 country.

Shengdong KeDepartment of Biological Sciences, Columbia University, 1212 Amsterdam Ave, MC 2433, New York, NY 10027, USA. sk2410@columbia.edu
Lawrence A Chasin
Columbia University · US

Funding

Exon recognition during constitutive pre-mRNA splicingR01GM072740 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI CHASIN, LAWRENCE ALLEN · 2005 to 2013
$3.1M
Exon recognition during constitutive pre-mRNA splicingR56GM072740 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI CHASIN, LAWRENCE ALLEN · 2009 to 2009
$292k
NIGMS NIH HHS GM072740
6 · The paper itself

Abstract

backgroundA very early step in splice site recognition is exon definition, a process that is as yet poorly understood. Communication between the two ends of an exon is thought to be required for this step. We report genome-wide evidence for exons being defined through the combinatorial activity of motifs located in flanking intronic regions.

resultsStrongly co-occurring motifs were found to specifically reside in four intronic regions surrounding a large number of human exons. These paired motifs occur around constitutive and alternative exons but not pseudo exons. Most co-occurring motifs are limited to intronic regions within 100 nucleotides of the exon. They are preferentially associated with weaker exons. Their pairing is conserved in evolution and they exhibit a lower frequency of single nucleotide polymorphism when paired. Paired motifs display specificity with respect to distance from the exon borders and in constitutive versus alternative splicing. Many resemble binding sites for heterogeneous nuclear ribonucleoproteins. Specific pairs are associated with tissue-specific genes, the higher expression of which coincides with that of the pertinent RNA binding proteins. Tested pairs acted synergistically to enhance exon inclusion, and this enhancement was found to be exon-specific.

conclusionsThe exon-flanking sequence pairs identified here by genomic analysis promote exon inclusion and may play a role in the exon definition step in pre-mRNA splicing. We propose a model in which multiple concerted interactions are required between exonic sequences and flanking intronic sequences to effect exon definition.

Indexed as

RNA SplicingAlgorithmsBase SequenceComputational BiologyExonsGenome, HumanGenomicsHumansIntronsModels, GeneticRNA PrecursorsRNA Precursors

Identifiers

PMID20704715
PMCPMC2945786
OpenAlexW2168574026

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.