Evidence map›Paper›PMID 17626050›Full record

ArticleNucleic acids research2007

A correlation with exon expression approach to identify cis-regulatory elements for tissue-specific alternative splicing.

Debopriya Das, Tyson A Clark, Anthony Schweitzer, Miki Yamamoto, Henry Marr, Josh Arribere, Simon Minovitsky, Alexander Poliakov, Inna Dubchak, John E Blume and 1 more

Abstract readEvaluation Study
In one paragraph

Article in Nucleic acids research, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing 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

52 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Sensitive period-regulating genetic pathways and exposure to adversity shape risk for depression.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
    Article
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  7. The regulatory genome of the malaria vectorNAR genomics and bioinformatics · 2021
    Article
  8. Review
  9. Developmental regulation of RNA processing by Rbfox proteins.Wiley interdisciplinary reviews. RNA · 2017
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. RNA binding proteins in the regulation of heart development.The international journal of biochemistry & cell biology · 2013
    Review
  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

11 authors.

Debopriya DasLife Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.
Tyson A Clark
Anthony Schweitzer
Miki Yamamoto
Henry Marr
Josh Arribere
Simon Minovitsky
Alexander Poliakov
Inna Dubchak
John E Blume
John G Conboy

Funding

RED CELL BAND 41--DEVELOPMENTAL CHANGES IN RNA SPLICINGR01HL045182 · NHLBI · UNIVERSITY OF CALIFORNIA BERKELEY · PI CONBOY, JOHN G · 1990 to 2010
$4.8M
Red Cell Band 4.1 - Developmental Changes in RNA SplicingR56HL045182 · NHLBI · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI CONBOY, JOHN G · 2008 to 2008
$500k
Programmed Changes in Alternative Splicing Within the Erythroid TranscriptomeR21DK075021 · NIDDK · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI CONBOY, JOHN G · 2006 to 2007
$462k
NHLBI NIH HHS HL45182NHLBI NIH HHS R01 HL045182NHLBI NIH HHS R56 HL045182NIDDK NIH HHS R21 DK075021
6 · The paper itself

Abstract

Correlation of motif occurrences with gene expression intensity is an effective strategy for elucidating transcriptional cis-regulatory logic. Here we demonstrate that this approach can also identify cis-regulatory elements for alternative pre-mRNA splicing. Using data from a human exon microarray, we identified 56 cassette exons that exhibited higher transcript-normalized expression in muscle than in other normal adult tissues. Intron sequences flanking these exons were then analyzed to identify candidate regulatory motifs for muscle-specific alternative splicing. Correlation of motif parameters with gene-normalized exon expression levels was examined using linear regression and linear splines on RNA words and degenerate weight matrices, respectively. Our unbiased analysis uncovered multiple candidate regulatory motifs for muscle-specific splicing, many of which are phylogenetically conserved among vertebrate genomes. The most prominent downstream motifs were binding sites for Fox1- and CELF-related splicing factors, and a branchpoint-like element acuaac; pyrimidine-rich elements resembling PTB-binding sites were most significant in upstream introns. Intriguingly, our systematic study indicates a paucity of novel muscle-specific elements that are dominant in short proximal intronic regions. We propose that Fox and CELF proteins play major roles in enforcing the muscle-specific alternative splicing program, facilitating expression of unique isoforms of cytoskeletal proteins critical to muscle cell function.

Indexed as

Alternative SplicingIntronsRegulatory Sequences, Ribonucleic AcidAnimalsBase SequenceBinding SitesComputational BiologyConserved SequenceCytoskeletal ProteinsExonsGene Expression ProfilingHumansMuscle, SkeletalMyocardiumRNA-Binding ProteinsRNA, MessengerCytoskeletal ProteinsRegulatory Sequences, Ribonucleic AcidRNA-Binding ProteinsRNA, MessengerRNA Precursors

Identifiers

PMID17626050
PMCPMC1950531

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.