Evidence map›Paper›PMID 28039323›Full record

ArticleNucleic acids research2017

Succession of splicing regulatory elements determines cryptic 5΄ss functionality.

Anna-Lena Brillen, Katrin Schöneweis, Lara Walotka, Linda Hartmann, Lisa Müller, Johannes Ptok, Wolfgang Kaisers, Gereon Poschmann, Kai Stühler, Emanuele Buratti and 2 more

Abstract read
In one paragraph

Article in Nucleic acids research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Let It Go: HIV-1Journal of virology · 2021
    Review
  8. Modifying splice site usage withComputational and structural biotechnology journal · 2021
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. 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

12 authors.

Anna-Lena BrillenInstitute for Virology, Heinrich-Heine-University Düsseldorf, 40225 Düsseldorf, Germany.
Katrin SchöneweisDepartment of Infectious Diseases, Molecular Virology, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Lara WalotkaInstitute for Virology, Heinrich-Heine-University Düsseldorf, 40225 Düsseldorf, Germany.
Linda HartmannInstitute for Virology, Heinrich-Heine-University Düsseldorf, 40225 Düsseldorf, Germany.
Lisa MüllerInstitute for Virology, Heinrich-Heine-University Düsseldorf, 40225 Düsseldorf, Germany.
Johannes PtokInstitute for Virology, Heinrich-Heine-University Düsseldorf, 40225 Düsseldorf, Germany.
Wolfgang KaisersDepartment of Anesthesiology, University Hospital Düsseldorf, Heinrich-Heine-University Düsseldorf, 40225 Düsseldorf, Germany.
Gereon PoschmannMolecular Proteomics Laboratory, BMFZ, Heinrich-Heine-University Düsseldorf, 40225 Düsseldorf, Germany.
Kai StühlerMolecular Proteomics Laboratory, BMFZ, Heinrich-Heine-University Düsseldorf, 40225 Düsseldorf, Germany.
Emanuele BurattiInternational Centre for Genetic Engineering and Biotechnology (ICGEB), Area Science Park, 34149 Trieste, Italy.
Stephan TheissInstitute of Clinical Neuroscience and Medical Psychology, Heinrich-Heine-University Düsseldorf, 40225.
Heiner SchaalInstitute for Virology, Heinrich-Heine-University Düsseldorf, 40225 Düsseldorf, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A critical step in exon definition is the recognition of a proper splice donor (5΄ss) by the 5' end of U1 snRNA. In the selection of appropriate 5΄ss, cis-acting splicing regulatory elements (SREs) are indispensable. As a model for 5΄ss recognition, we investigated cryptic 5΄ss selection within the human fibrinogen Bβ-chain gene (FGB) exon 7, where we identified several exonic SREs that simultaneously acted on up- and downstream cryptic 5΄ss. In the FGB exon 7 model system, 5΄ss selection iteratively proceeded along an alternating sequence of U1 snRNA binding sites and interleaved SREs which in principle supported different 3' exon ends. Like in a relay race, SREs either suppressed a potential 5΄ss and passed the splicing baton on or splicing actually occurred. From RNA-Seq data, we systematically selected 19 genes containing exons with silent U1 snRNA binding sites competing with nearby highly used 5΄ss. Extensive SRE analysis by different algorithms found authentic 5΄ss significantly more supported by SREs than silent U1 snRNA binding sites, indicating that our concept may permit generalization to a model for 5΄ss selection and 3' exon end definition.

Indexed as

Regulatory Sequences, Ribonucleic AcidRNA Splice SitesExonsFibrinogenHeLa CellsHumansMutationRNA, Small NuclearSerine-Arginine Splicing FactorsFGB protein, humanFibrinogenRegulatory Sequences, Ribonucleic AcidRNA, Small NuclearRNA Splice SitesSerine-Arginine Splicing FactorsU1 small nuclear RNA

Identifiers

PMID28039323
PMCPMC5397162

What OpenQuestion holds

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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.