Evidence map›Paper›PMID 20048052›Full record

ArticleMolecular and cellular biology2010

Sterile alpha motif domain-mediated self-association plays an essential role in modulating the activity of the Drosophila ETS family transcriptional repressor Yan.

Jie Zhang, Thomas G W Graham, Pavithra Vivekanand, Lauren Cote, Maureen Cetera, Ilaria Rebay

Abstract read
In one paragraph

Article in Molecular and cellular biology, 2010. 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
1.9field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
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  4. Sticky, Adaptable, and Many-sided: SAM protein versatility in normal and pathological hematopoietic states.BioEssays : news and reviews in molecular, cellular and developmental biology · 2023
    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

6 authors at 3 institutions in 2 countries.

Jie ZhangUniversity of Chicago, Ben May Department for Cancer Research, Chicago, IL 60637, USA.
Thomas G W Graham
Pavithra Vivekanand
Lauren Cote
Maureen Cetera
Ilaria Rebay
University of Chicago · USFranklin & Marshall College · USUniversity of Cambridge · GB

Funding

CORE: ADMINISTRATIVEP50GM081892 · NIGMS · UNIVERSITY OF CHICAGO · PI WHITE, KEVIN P. · 2008 to 2013
$15.9M
Function and Regulation of the ETS Transcriptional Repressor Tel-1/YANR01GM080372 · NIGMS · UNIVERSITY OF CHICAGO · PI REBAY, ILARIA · 2007 to 2022
$3.9M
Undergraduate Training Program in Chemical & Physical B*T90DK070076 · NIDDK · UNIVERSITY OF CHICAGO · PI KRON, STEPHEN J. · 2006 to 2007
$550k
NIDDK NIH HHS T90 DK070076NIDDK NIH HHS T90-DK070076NIGMS NIH HHS P50 GM081892NIGMS NIH HHS R01 GM080372NIGMS NIH HHS R01 GM80372
6 · The paper itself

Abstract

The ETS family transcriptional repressor Yan is an important downstream target and effector of the receptor tyrosine kinase (RTK) signaling pathway in Drosophila melanogaster. Structural and biochemical studies have shown that the N-terminal sterile alpha motif (SAM) of Yan is able to self associate to form a helical polymeric structure in vitro, although the extent and functional significance of self-association of full-length Yan remain unclear. In this study, we demonstrated that full-length Yan self associates via its SAM domain to form higher-order complexes in living cells. Introduction of SAM domain missense mutations that restrict Yan to a monomeric state reduces Yan's transcriptional repression activity and impairs its function during embryonic and retinal development. Coexpression of combinations of SAM domain mutations that permit the formation of Yan dimers, but not higher-order oligomers, increases activity relative to that of monomeric Yan, but not to the level obtained with wild-type Yan. Mechanistically, self-association directly promotes transcriptional repression of target genes independent of its role in limiting mitogen-activated protein kinase (MAPK)-mediated phosphorylation and nuclear export of Yan. Thus, we propose that the formation of higher-order Yan oligomers contributes to proper repression of target gene expression and RTK signaling output in developing tissues.

Indexed as

AnimalsAnimals, Genetically ModifiedBase SequenceCell LineDNA PrimersDrosophila melanogasterDrosophila ProteinsEyeEye ProteinsFluorescence Recovery After PhotobleachingGene Expression Regulation, DevelopmentalGenes, InsectGreen Fluorescent ProteinsMAP Kinase Signaling SystemMutation, MissensePhosphorylationAOP protein, DrosophilaDNA PrimersDrosophila Proteinsenhanced green fluorescent proteinEye ProteinsGreen Fluorescent ProteinsProto-Oncogene Proteins c-etsReceptor Protein-Tyrosine KinasesRecombinant Fusion ProteinsRepressor Proteins

Identifiers

PMID20048052
PMCPMC2820895
OpenAlexW2159205683

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.