Evidence map›Paper›PMID 26647463›Full record

ArticleRNA (New York, N.Y.)2016

Sequencing of lariat termini in S. cerevisiae reveals 5' splice sites, branch points, and novel splicing events.

Daoming Qin, Lei Huang, Alissa Wlodaver, Jorge Andrade, Jonathan P Staley

Open access · bronzeAbstract read
In one paragraph

Article in RNA (New York, N.Y.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

29 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Impact on splicing inRNA (New York, N.Y.) · 2023
    Article
  7. Review
  8. Article
  9. Article
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  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Pre-mRNA Splicing in the Nuclear Landscape.Cold Spring Harbor symposia on quantitative biology · 2019
    Article
  18. Article
  19. Article
  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

5 authors at 2 institutions in 1 country.

Daoming QinDepartment of Molecular Genetics and Cell Biology, University of Chicago, Chicago, Illinois 60637, USA.
Lei HuangCenter for Research Informatics, University of Chicago, Chicago, Illinois 60637, USA.
Alissa WlodaverDepartment of Molecular Genetics and Cell Biology, University of Chicago, Chicago, Illinois 60637, USA.
Jorge AndradeCenter for Research Informatics, University of Chicago, Chicago, Illinois 60637, USA.
Jonathan P StaleyDepartment of Molecular Genetics and Cell Biology, University of Chicago, Chicago, Illinois 60637, USA.
University of Chicago · USUniversity of Illinois Chicago · US

Funding

TRANSLATIONAL RESEARCH UNIVERSITY OF CHICAGO: CLINICAL TRIALSUL1RR024999 · NCRR · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2007 to 2011
$25.3M
Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
Mechanisms for Rearranging RNA during Pre-mRNA Splicing - Renewal 01R01GM062264 · NIGMS · UNIVERSITY OF CHICAGO · PI STALEY, JONATHAN P · 2001 to 2019
$5.3M
Analyzing pre-mRNA splicing by deep sequencing of splice sitesR21HG005262 · NHGRI · UNIVERSITY OF CHICAGO · PI STALEY, JONATHAN P · 2010 to 2011
$455k
NCATS NIH HHS UL1 TR000430NCRR NIH HHS UL1 RR024999NHGRI NIH HHS R21 HG005262NHGRI NIH HHS R21HG5262NIGMS NIH HHS R01 GM062264NIGMS NIH HHS R01GM62264
6 · The paper itself

Abstract

Pre-mRNA splicing is a central step in the shaping of the eukaryotic transcriptome and in the regulation of gene expression. Yet, due to a focus on fully processed mRNA, common approaches for defining pre-mRNA splicing genome-wide are suboptimal-especially with respect to defining the branch point sequence, a key cis-element that initiates the chemistry of splicing. Here, we report a complementary intron-centered approach designed to more efficiently, simply, and directly define splicing events genome-wide. Specifically, we developed a method distinguished by deep sequencing of lariat intron termini (LIT-seq). In a test of LIT-seq using the budding yeast Saccharomyces cerevisiae, we not only successfully captured the majority of annotated, expressed splicing events but also uncovered 45 novel splicing events, establishing the sensitivity of LIT-seq. Moreover, our libraries were highly enriched with reads that reported on splice sites; by a simple and direct inspection of sequencing reads, we empirically defined both 5' splice sites and branch sites, as well as their consensus sequences, with nucleotide resolution. Additionally, our study revealed that the 3' termini of lariat introns are subject to nontemplated addition of adenosines, characteristic of signals sensed by 3' to 5' RNA turnover machinery. Collectively, this work defines a novel, genome-wide approach for analyzing splicing with unprecedented depth, specificity, and resolution.

Indexed as

Genome, FungalBase SequenceGene Expression Regulation, FungalIntronsMolecular Sequence DataMutationNucleic Acid ConformationRNA, FungalRNA NucleotidyltransferasesRNA PrecursorsRNA Splice SitesRNA SplicingSaccharomyces cerevisiaeSpliceosomeslariat debranching enzymeRNA, FungalRNA NucleotidyltransferasesRNA PrecursorsRNA Splice Sitesbranch-pointlariat intronpre-mRNA splicingRNA-seqsplice site

Identifiers

PMID26647463
PMCPMC4712674
OpenAlexW2196128333

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.