Evidence map›Paper›PMID 25775193›Full record

ArticleRNA biology2015

TINTIN, at the interface of chromatin, transcription elongation, and mRNA processing.

Wajid Bhat, Salar Ahmad, Jacques Côté

Open access · bronzeAbstract read
In one paragraph

Article in RNA biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Building a KATalogue of acetyllysine targeting and function.Briefings in functional genomics · 2016
    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

3 authors at 2 institutions in 2 countries.

Wajid Bhata St-Patrick Research Group in Basic Oncology; Laval University Cancer Research Center; CHU de Quebec Research Center-Oncology Axis; Hôtel-Dieu de Québec (CHU de Québec) ; Quebec City , Quebec , Canada.
Salar Ahmad
Jacques Côté
Cancer Research Center · USSt. Patrick Hospital · US

Funding

Canadian Institutes of Health Research MOP-14308
6 · The paper itself

Abstract

Recent work including high-resolution genome-wide analysis uncovered a new trimeric complex involved in transcription elongation, both as an integral part of the NuA4 histone acetyltransferase and as an independent functional entity. The complex is conserved in eukaryotes and is named TINTIN, for Trimer Independent of NuA4 for transcription Interactions with Nucleosomes. This point of view covers the current knowledge regarding TINTIN's function in modulating chromatin structure and influencing transcription elongation in eukaryotes. It also points to several physical and functional links to co-transcriptional processes, including interactions with the mRNA splicing machinery and the nuclear exosome.

Indexed as

Transcription Elongation, GeneticAnimalsChromatinHumansMultiprotein ComplexesNucleosomesRNA, MessengerRNA Processing, Post-TranscriptionalChromatinMultiprotein ComplexesNucleosomesRNA, MessengeracetylationchromatinEaf3Eaf5Eaf7MRG15MRGBPNuA4TINTINtranscription elongation

Identifiers

PMID25775193
PMCPMC4615837
OpenAlexW1579526033

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.