Evidence map›Paper›PMID 21725360›Full record

ArticleOncogene2012

And-1 is required for the stability of histone acetyltransferase Gcn5.

Y Li, A N Jaramillo-Lambert, Y Yang, R Williams, N H Lee, W Zhu

Abstract read
In one paragraph

Article in Oncogene, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

28 citing papers in PubMed, 34 citations in OpenAlex.

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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 1 institution in 1 country.

Y LiDepartment of Biochemistry and Molecular Biology, The George Washington University Medical School, Washington, DC 20037, USA.
A N Jaramillo-Lambert
Y Yang
R Williams
N H Lee
W Zhu
George Washington University · US

Funding

Mapping Gene Networks in Colon CancerR01CA120316 · NCI · GEORGE WASHINGTON UNIVERSITY · PI LEE, NORMAN H · 2007 to 2010
$1.6M
DNA Replication Control and Its Application to Selective Killing of Cancer CellsR00CA136555 · NCI · GEORGE WASHINGTON UNIVERSITY · PI ZHU, WENGE · 2010 to 2012
$732k
NCI NIH HHS 4R00CA136555NCI NIH HHS CA120316NCI NIH HHS R00 CA136555NCI NIH HHS R01 CA120316
6 · The paper itself

Abstract

Histone acetyltransferases (HATs) have a central role in the modification of chromatin as well as in the pathogenesis of a broad set of diseases including cancers. Gcn5 is the first identified transcription-related HAT that has been implicated in the regulation of diverse cellular functions. However, how Gcn5 proteins are regulated remains largely unknown. Here we show that acidic nucleoplasmic DNA-binding protein (And-1, a high mobility group domain-containing protein) has remarkable capability to regulate the stability of Gcn5 proteins and thereby histone H3 acetylation. We find that And-1 forms a complex with both histone H3 and Gcn5. Downregulation of And-1 results in Gcn5 degradation, leading to the reduction of H3K9 and H3K56 acetylation. And-1 overexpression stabilizes Gcn5 through protein-protein interactions in vivo. Furthermore, And-1 expression is increased in cancer cells in a manner correlating with increased Gcn5 and H3K9Ac and H3K56Ac. Thus, our data reveal not only a functional link between Gcn5 and And-1 that is essential for Gcn5 protein stability and histone H3 acetylation, but also a potential role of And-1 in cancer.

Indexed as

AcetylationCell CycleCell LineCell Line, TumorChromatin ImmunoprecipitationDNA-Binding ProteinsHCT116 CellsHEK293 CellsHeLa CellsHistonesHumansImmunoblottingLysineNeoplasmsp300-CBP-Associated Factorp300-CBP Transcription FactorsDNA-Binding ProteinsHistonesLysinep300-CBP-Associated Factorp300-CBP Transcription FactorsWDHD1 protein, human

Identifiers

PMID21725360
PMCPMC3191320
OpenAlexW2033003216

What OpenQuestion holds

Textmetadata
LicenceTDM
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.