Evidence map›Paper›PMID 23172856›Full record

ArticleGenetics2013

The relationship between long-range chromatin occupancy and polymerization of the Drosophila ETS family transcriptional repressor Yan.

Jemma L Webber, Jie Zhang, Lauren Cote, Pavithra Vivekanand, Xiaochun Ni, Jie Zhou, Nicolas Nègre, Richard W Carthew, Kevin P White, Ilaria Rebay

Abstract read
In one paragraph

Article in Genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
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  8. Polycomb group (PcG) proteins and Pax6 cooperate to inhibitDevelopment (Cambridge, England) · 2018
    Article
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  14. Review
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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

10 authors.

Jemma L WebberBen May Department for Cancer Research, University of Chicago, Chicago, IL 60637, USA.
Jie Zhang
Lauren Cote
Pavithra Vivekanand
Xiaochun Ni
Jie Zhou
Nicolas Nègre
Richard W Carthew
Kevin P White
Ilaria Rebay

Funding

CORE: ADMINISTRATIVEP50GM081892 · NIGMS · UNIVERSITY OF CHICAGO · PI WHITE, KEVIN P. · 2008 to 2013
$15.9M
Molecular Mechanisms of Gene Silencing by RNAiR01GM068743 · NIGMS · NORTHWESTERN UNIVERSITY · PI CARTHEW, RICHARD W. · 2003 to 2014
$4.1M
Function and Regulation of the ETS Transcriptional Repressor Tel-1/YANR01GM080372 · NIGMS · UNIVERSITY OF CHICAGO · PI REBAY, ILARIA · 2007 to 2022
$3.9M
MicroRNA Regulation of Biological MechanismsR01GM077581 · NIGMS · NORTHWESTERN UNIVERSITY · PI CARTHEW, RICHARD W. · 2006 to 2015
$2.9M
NIGMS NIH HHS P50 GM081892NIGMS NIH HHS R01 GM068743NIGMS NIH HHS R01 GM077581NIGMS NIH HHS R01 GM080372NIGMS NIH HHS R01 GM80372
6 · The paper itself

Abstract

ETS family transcription factors are evolutionarily conserved downstream effectors of Ras/MAPK signaling with critical roles in development and cancer. In Drosophila, the ETS repressor Yan regulates cell proliferation and differentiation in a variety of tissues; however, the mechanisms of Yan-mediated repression are not well understood and only a few direct target genes have been identified. Yan, like its human ortholog TEL1, self-associates through an N-terminal sterile α-motif (SAM), leading to speculation that Yan/TEL1 polymers may spread along chromatin to form large repressive domains. To test this hypothesis, we created a monomeric form of Yan by recombineering a point mutation that blocks SAM-mediated self-association into the yan genomic locus and compared its genome-wide chromatin occupancy profile to that of endogenous wild-type Yan. Consistent with the spreading model predictions, wild-type Yan-bound regions span multiple kilobases. Extended occupancy patterns appear most prominent at genes encoding crucial developmental regulators and signaling molecules and are highly conserved between Drosophila melanogaster and D. virilis, suggesting functional relevance. Surprisingly, although occupancy is reduced, the Yan monomer still makes extensive multikilobase contacts with chromatin, with an overall pattern similar to that of wild-type Yan. Despite its near-normal chromatin recruitment, the repressive function of the Yan monomer is significantly impaired, as evidenced by elevated target gene expression and failure to rescue a yan null mutation. Together our data argue that SAM-mediated polymerization contributes to the functional output of the active Yan repressive complexes that assemble across extended stretches of chromatin, but does not directly mediate recruitment to DNA or chromatin spreading.

Indexed as

Protein MultimerizationAmino Acid MotifsAnimalsChromatinDrosophilaDrosophila ProteinsEye ProteinsGene ExpressionGenome, InsectMutationProtein BindingProtein Structure, TertiaryRepressor ProteinsAOP protein, DrosophilaChromatinDrosophila ProteinsEye ProteinsRepressor Proteins

Identifiers

PMID23172856
PMCPMC3567750

What OpenQuestion holds

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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.