Evidence map›Paper›PMID 23109428›Full record

ArticleMolecular and cellular biology2013

Effects of the Paf1 complex and histone modifications on snoRNA 3'-end formation reveal broad and locus-specific regulation.

Brett N Tomson, Elia M Crisucci, Lawrence E Heisler, Marinella Gebbia, Corey Nislow, Karen M Arndt

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

21 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Rtf1 Transcriptionally Regulates Neonatal and Adult Cardiomyocyte Biology.Journal of cardiovascular development and disease · 2023
    Article
  8. Review
  9. Article
  10. Article
  11. RNA Binding by Histone Methyltransferases Set1 and Set2.Molecular and cellular biology · 2017
    Article
  12. Different phosphoisoforms of RNA polymerase II engage the Rtt103 termination factor in a structurally analogous manner.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

6 authors at 2 institutions in 3 countries.

Brett N TomsonDepartment of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Elia M Crisucci
Lawrence E Heisler
Marinella Gebbia
Corey Nislow
Karen M Arndt
University of Pittsburgh · USUniversity of Toronto · CA

Funding

TRANSCRIPTION FACTOR MUTANTS OF YEASTR01GM052593 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ARNDT, KAREN M · 1995 to 2020
$7.9M
Mechanisms Underlying Regulation of Non-Coding RNA TranscriptionF32GM093383 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI TOMSON, BRETT NEUMAN · 2010 to 2012
$153k
CIHR MOP-84305NIGMS NIH HHS F32 GM093383NIGMS NIH HHS F32GM093383NIGMS NIH HHS R01 GM052593NIGMS NIH HHS R01-GM52593
6 · The paper itself

Abstract

Across diverse eukaryotes, the Paf1 complex (Paf1C) plays critical roles in RNA polymerase II transcription elongation and regulation of histone modifications. Beyond these roles, the human and Saccharomyces cerevisiae Paf1 complexes also interact with RNA 3'-end processing components to affect transcript 3'-end formation. Specifically, the Saccharomyces cerevisiae Paf1C functions with the RNA binding proteins Nrd1 and Nab3 to regulate the termination of at least two small nucleolar RNAs (snoRNAs). To determine how Paf1C-dependent functions regulate snoRNA formation, we used high-density tiling arrays to analyze transcripts in paf1Δ cells and uncover new snoRNA targets of Paf1. Detailed examination of Paf1-regulated snoRNA genes revealed locus-specific requirements for Paf1-dependent posttranslational histone modifications. We also discovered roles for the transcriptional regulators Bur1-Bur2, Rad6, and Set2 in snoRNA 3'-end formation. Surprisingly, at some snoRNAs, this function of Rad6 appears to be primarily independent of its role in histone H2B monoubiquitylation. Cumulatively, our work reveals a broad requirement for the Paf1C in snoRNA 3'-end formation in S. cerevisiae, implicates the participation of transcriptional proteins and histone modifications in this process, and suggests that the Paf1C contributes to the fine tuning of nuanced levels of regulation that exist at individual loci.

Indexed as

Gene Expression Regulation, FungalCell Cycle ProteinsCyclin-Dependent KinasesCyclinsHistonesMethyltransferasesMutationNuclear ProteinsProtein Processing, Post-TranslationalRNA, Small NucleolarSaccharomyces cerevisiae ProteinsTATA-Box Binding ProteinTranscriptional Elongation FactorsUbiquitinationUbiquitin-Conjugating EnzymesBur2 protein, S cerevisiaeCell Cycle ProteinsCTR9 protein, S cerevisiaeCyclin-Dependent KinasesCyclinsHistonesMethyltransferasesNuclear ProteinsPAF1 protein, S cerevisiaeRAD6 protein, S cerevisiaeRNA, Small NucleolarRTF1 protein, S cerevisiaeSaccharomyces cerevisiae ProteinsSet2 protein, S cerevisiaeSGV1 protein, S cerevisiaeTATA-Box Binding ProteinTranscriptional Elongation FactorsUbiquitin-Conjugating Enzymes

Identifiers

PMID23109428
PMCPMC3536304
OpenAlexW2105064729

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.