Evidence map›Paper›PMID 25815464›Full record

ArticlePLoS genetics2015

GAGA factor maintains nucleosome-free regions and has a role in RNA polymerase II recruitment to promoters.

Nicholas J Fuda, Michael J Guertin, Sumeet Sharma, Charles G Danko, André L Martins, Adam Siepel, John T Lis

Abstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing 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

76 citing papers in PubMed.

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  15. bioRxiv : the preprint server for biology · 2024
    Article
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16 more citing papers are in PubMed but not listed here.

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

7 authors.

Nicholas J FudaDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, New York, United States of America.
Michael J GuertinDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, New York, United States of America.
Sumeet SharmaDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, New York, United States of America.
Charles G DankoDepartment of Biological Statistics and Computational Biology, Cornell University, Ithaca, New York, United States of America.
André L MartinsDepartment of Biological Statistics and Computational Biology, Cornell University, Ithaca, New York, United States of America.
Adam SiepelDepartment of Biological Statistics and Computational Biology, Cornell University, Ithaca, New York, United States of America.
John T LisDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, New York, United States of America.

Funding

PREDOCTORAL TRAINING IN CELLULAR AND MOLECULAR BIOLOGYT32GM007273 · NIGMS · CORNELL UNIVERSITY ITHACA · PI BRETSCHER, ANTHONY P. · 1985 to 2019
$11.6M
COORDINATE GENE REGULATION IN ANIMAL CELLSR01GM025232 · NIGMS · CORNELL UNIVERSITY ITHACA · PI LIS, JOHN T · 1985 to 2020
$8.4M
COORDINATE GENE REGULATION IN ANIMAL CELLSR37GM025232 · NIGMS · CORNELL UNIVERSITY ITHACA · PI LIS, JOHN THOMAS · 1995 to 2004
$2.5M
NIGMS NIH HHS GM25232NIGMS NIH HHS R01 GM025232NIGMS NIH HHS R37 GM025232NIGMS NIH HHS T32 GM007273
6 · The paper itself

Abstract

Previous studies have shown that GAGA Factor (GAF) is enriched on promoters with paused RNA Polymerase II (Pol II), but its genome-wide function and mechanism of action remain largely uncharacterized. We assayed the levels of transcriptionally-engaged polymerase using global run-on sequencing (GRO-seq) in control and GAF-RNAi Drosophila S2 cells and found promoter-proximal polymerase was significantly reduced on a large subset of paused promoters where GAF occupancy was reduced by knock down. These promoters show a dramatic increase in nucleosome occupancy upon GAF depletion. These results, in conjunction with previous studies showing that GAF directly interacts with nucleosome remodelers, strongly support a model where GAF directs nucleosome displacement at the promoter and thereby allows the entry Pol II to the promoter and pause sites. This action of GAF on nucleosomes is at least partially independent of paused Pol II because intergenic GAF binding sites with little or no Pol II also show GAF-dependent nucleosome displacement. In addition, the insulator factor BEAF, the BEAF-interacting protein Chriz, and the transcription factor M1BP are strikingly enriched on those GAF-associated genes where pausing is unaffected by knock down, suggesting insulators or the alternative promoter-associated factor M1BP protect a subset of GAF-bound paused genes from GAF knock-down effects. Thus, GAF binding at promoters can lead to the local displacement of nucleosomes, but this activity can be restricted or compensated for when insulator protein or M1BP complexes also reside at GAF bound promoters.

Indexed as

Transcription, GeneticAnimalsBinding SitesDNA-Binding ProteinsDrosophila melanogasterDrosophila ProteinsEye ProteinsGene Knockdown TechniquesNucleosomesPromoter Regions, GeneticRNA Polymerase IITranscription FactorsBEAF-32 protein, DrosophilaDNA-Binding ProteinsDrosophila ProteinsEye ProteinsM1BP protein, DrosophilaNucleosomesRNA Polymerase IITranscription FactorsTrl protein, Drosophila

Identifiers

PMID25815464
PMCPMC4376892

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Registered trials

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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.