Evidence map›Paper›PMID 27288397›Full record

ArticleMolecular systems biology2016

Strand-specific, high-resolution mapping of modified RNA polymerase II.

Laura Milligan, Vân A Huynh-Thu, Clémentine Delan-Forino, Alex Tuck, Elisabeth Petfalski, Rodrigo Lombraña, Guido Sanguinetti, Grzegorz Kudla, David Tollervey

Abstract read
In one paragraph

Article in Molecular systems biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Using TTNature protocols · 2020
    Article
  11. Article
  12. Nascent RNA and the Coordination of Splicing with Transcription.Cold Spring Harbor perspectives in biology · 2019
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  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

9 authors.

Laura MilliganWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh, UK.
Vân A Huynh-ThuSchool of Informatics, University of Edinburgh, Edinburgh, UK Department of Electrical Engineering and Computer Science, University of Liège, Liège, Belgium.
Clémentine Delan-ForinoWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh, UK.
Alex TuckWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh, UK Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI) Wellcome Trust Genome Campus, Cambridge, UK.
Elisabeth PetfalskiWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh, UK.
Rodrigo LombrañaMRC Human Genetics Unit, IGMM, University of Edinburgh, Edinburgh, UK.
Guido SanguinettiSchool of Informatics, University of Edinburgh, Edinburgh, UK d.tollervey@ed.ac.uk gkudla@gmail.com gsanguin@inf.ed.ac.uk.
Grzegorz KudlaMRC Human Genetics Unit, IGMM, University of Edinburgh, Edinburgh, UK d.tollervey@ed.ac.uk gkudla@gmail.com gsanguin@inf.ed.ac.uk.ORCID 0000-0002-7924-2744
David TollerveyWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh, UK d.tollervey@ed.ac.uk gkudla@gmail.com gsanguin@inf.ed.ac.uk.ORCID 0000-0003-2894-2772

Funding

Biotechnology and Biological Sciences Research Council BB/F010656/1European Research Council 306999Medical Research Council MC_UU_12018/23Wellcome Trust 077248Wellcome Trust 092076Wellcome Trust 097383Wellcome Trust 103977
6 · The paper itself

Abstract

Reversible modification of the RNAPII C-terminal domain links transcription with RNA processing and surveillance activities. To better understand this, we mapped the location of RNAPII carrying the five types of CTD phosphorylation on the RNA transcript, providing strand-specific, nucleotide-resolution information, and we used a machine learning-based approach to define RNAPII states. This revealed enrichment of Ser5P, and depletion of Tyr1P, Ser2P, Thr4P, and Ser7P in the transcription start site (TSS) proximal ~150 nt of most genes, with depletion of all modifications close to the poly(A) site. The TSS region also showed elevated RNAPII relative to regions further 3', with high recruitment of RNA surveillance and termination factors, and correlated with the previously mapped 3' ends of short, unstable ncRNA transcripts. A hidden Markov model identified distinct modification states associated with initiating, early elongating and later elongating RNAPII. The initiation state was enriched near the TSS of protein-coding genes and persisted throughout exon 1 of intron-containing genes. Notably, unstable ncRNAs apparently failed to transition into the elongation states seen on protein-coding genes.

Indexed as

Binding SitesMachine LearningMarkov ChainsPhosphorylationRNA, FungalRNA, MessengerRNA Polymerase IISaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsTranscription, GeneticRNA, FungalRNA, MessengerRNA Polymerase IISaccharomyces cerevisiae Proteinshidden Markov modelpolymerase CTD phosphorylationtranscriptionyeast

Identifiers

PMID27288397
PMCPMC4915518

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.