Evidence map›Paper›PMID 19155327›Full record

ArticleRNA (New York, N.Y.)2009

Splicing of designer exons reveals unexpected complexity in pre-mRNA splicing.

Xiang H-F Zhang, Mauricio A Arias, Shengdong Ke, Lawrence A Chasin

Abstract read
In one paragraph

Article in RNA (New York, N.Y.), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

  1. Article
  2. Deciphering RNA splicing logic with interpretable machine learning.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  3. Review
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  15. Introns and gene expression: cellular constraints, transcriptional regulation, and evolutionary consequences.BioEssays : news and reviews in molecular, cellular and developmental biology · 2015
    Article
  16. Article
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  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

4 authors.

Xiang H-F ZhangDepartment of Biological Sciences, Columbia University, New York, New York 10027, USA.
Mauricio A Arias
Shengdong Ke
Lawrence A Chasin

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 GM072740NIGMS NIH HHS R01 GM072740NIGMS NIH HHS R56 GM072740
6 · The paper itself

Abstract

Pre-messengerRNA (mRNA) splicing requires the accurate recognition of splice sites by the cellular RNA processing machinery. In addition to sequences that comprise the branchpoint and the 3' and 5' splice sites, the cellular splicing machinery relies on additional information in the form of exonic and intronic splicing enhancer and silencer sequences. The high abundance of these motifs makes it difficult to investigate their effects using standard genetic perturbations, since their disruption often leads to the formation of yet new elements. To lessen this problem, we have designed synthetic exons comprised of multiple copies of a single prototypical exonic enhancer and a single prototypical exonic silencer sequence separated by neutral spacer sequences. The spacer sequences buffer the exon against the formation of new elements as the number and order of the original elements are varied. Over 100 such designer exons were constructed by random ligation of enhancer, silencer, and neutral elements. Each exon was positioned as the central exon in a 3-exon minigene and tested for exon inclusion after transient transfection. The level of inclusion of the test exons was seen to be dependent on the provision of enhancers and could be decreased by the provision of silencers. In general, there was a good quantitative correlation between the proportion of enhancers and splicing. However, widely varying inclusion levels could be produced by different permutations of the enhancer and silencer elements, indicating that even in this simplified system splicing decisions rest on complex interplays of yet to be determined parameters.

Indexed as

ExonsRegulatory Sequences, Ribonucleic AcidRNA Splice SitesAnimalsCricetinaeCricetulusHumansRNA, MessengerRNA SplicingRegulatory Sequences, Ribonucleic AcidRNA, MessengerRNA Splice Sites

Identifiers

PMID19155327
PMCPMC2657016

What OpenQuestion holds

Textmetadata
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.