Evidence map›Paper›PMID 27473169›Full record

ArticleRNA (New York, N.Y.)2016

Identification of new branch points and unconventional introns in Saccharomyces cerevisiae.

Genevieve M Gould, Joseph M Paggi, Yuchun Guo, David V Phizicky, Boris Zinshteyn, Eric T Wang, Wendy V Gilbert, David K Gifford, Christopher B Burge

Abstract 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 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

  1. Article
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  4. Review
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  16. Pre-mRNA modifications and their role in nuclear processing.Quantitative biology (Beijing, China) · 2018
    Article
  17. Article
  18. Tracing themBio · 2018
    Article
  19. Article
  20. Review
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

9 authors.

Genevieve M GouldDepartment of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Joseph M PaggiDepartment of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA Computer Science and Artificial Intelligence Laboratory, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Yuchun GuoComputer Science and Artificial Intelligence Laboratory, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
David V PhizickyDepartment of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Boris ZinshteynDepartment of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Eric T WangDepartment of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Wendy V GilbertDepartment of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
David K GiffordComputer Science and Artificial Intelligence Laboratory, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Christopher B BurgeDepartment of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.

Funding

PRE-DOCTORAL TRAINING IN THE BIOLOGICAL SCIENCEST32GM007287 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BELL, STEPHEN P., KEATING, AMY E · 1985 to 2019
$40.8M
Regulation and Function of snoRNA GenesR01GM101316 · NIGMS · YALE UNIVERSITY · PI Wendy Victoria Gilbert · 2014 to 2026
$3.9M
NIGMS NIH HHS R01 GM101316NIGMS NIH HHS T32 GM007287
6 · The paper itself

Abstract

Spliced messages constitute one-fourth of expressed mRNAs in the yeast Saccharomyces cerevisiae, and most mRNAs in metazoans. Splicing requires 5' splice site (5'SS), branch point (BP), and 3' splice site (3'SS) elements, but the role of the BP in splicing control is poorly understood because BP identification remains difficult. We developed a high-throughput method, Branch-seq, to map BPs and 5'SSs of isolated RNA lariats. Applied to S. cerevisiae, Branch-seq detected 76% of expressed, annotated BPs and identified a comparable number of novel BPs. We performed RNA-seq to confirm associated 3'SS locations, identifying some 200 novel splice junctions, including an AT-AC intron. We show that several yeast introns use two or even three different BPs, with effects on 3'SS choice, protein coding potential, or RNA stability, and identify novel introns whose splicing changes during meiosis or in response to stress. Together, these findings show unanticipated complexity of splicing in yeast.

Indexed as

IntronsRNA Splice SitesNucleotide MotifsRNA SplicingSaccharomyces cerevisiaeSequence Analysis, RNARNA Splice Sitesbranch point sequencepre-mRNA splicingstress response

Identifiers

PMID27473169
PMCPMC5029451

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.