Evidence map›Paper›PMID 27198229›Full record

ArticleGenes & development2016

The Enok acetyltransferase complex interacts with Elg1 and negatively regulates PCNA unloading to promote the G1/S transition.

Fu Huang, Anita Saraf, Laurence Florens, Thomas Kusch, Selene K Swanson, Leanne T Szerszen, Ge Li, Arnob Dutta, Michael P Washburn, Susan M Abmayr and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Tctp, a unique Ing5-binding partner, inhibits the chromatin binding of Enok inProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  5. Review
  6. Article
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  8. Article
  9. Review
  10. Review
  11. Article
  12. 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

11 authors at 4 institutions in 2 countries.

Fu HuangStowers Institute for Medical Research, Kansas City, Missouri 64110, USA; Institute of Biological Chemistry, Academia Sinica, Taipei 11529, Taiwan;
Anita SarafStowers Institute for Medical Research, Kansas City, Missouri 64110, USA;
Laurence FlorensStowers Institute for Medical Research, Kansas City, Missouri 64110, USA;
Thomas KuschDepartment of Molecular Biology and Biochemistry, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854, USA;
Selene K SwansonStowers Institute for Medical Research, Kansas City, Missouri 64110, USA;
Leanne T SzerszenStowers Institute for Medical Research, Kansas City, Missouri 64110, USA;
Ge LiStowers Institute for Medical Research, Kansas City, Missouri 64110, USA;
Arnob DuttaStowers Institute for Medical Research, Kansas City, Missouri 64110, USA;
Michael P WashburnStowers Institute for Medical Research, Kansas City, Missouri 64110, USA; Pathology and Laboratory Medicine, University of Kansas Medical Center, Kansas City, Kansas 66160, USA;
Susan M AbmayrStowers Institute for Medical Research, Kansas City, Missouri 64110, USA; Department of Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City, Kansas 66160, USA.
Jerry L WorkmanStowers Institute for Medical Research, Kansas City, Missouri 64110, USA;
Stowers Institute for Medical Research · USInstitute of Biological Chemistry, Academia Sinica · TWRutgers, The State University of New Jersey · USUniversity of Kansas Medical Center · US

Funding

Transcription regulation in chromatinR35GM118068 · NIGMS · STOWERS INSTITUTE FOR MEDICAL RESEARCH · PI JERRY L WORKMAN · 2016 to 2026
$4.2M
Analysis of metazoan SAGA complex function in gene expressionR01GM099945 · NIGMS · STOWERS INSTITUTE FOR MEDICAL RESEARCH · PI ABMAYR, SUSAN M, WORKMAN, JERRY L · 2012 to 2015
$1.2M
NIGMS NIH HHS R01 GM099945NIGMS NIH HHS R35 GM118068
6 · The paper itself

Abstract

KAT6 histone acetyltransferases (HATs) are highly conserved in eukaryotes and are involved in cell cycle regulation. However, information regarding their roles in regulating cell cycle progression is limited. Here, we report the identification of subunits of the Drosophila Enok complex and demonstrate that all subunits are important for its HAT activity. We further report a novel interaction between the Enok complex and the Elg1 proliferating cell nuclear antigen (PCNA)-unloader complex. Depletion of Enok in S2 cells resulted in a G1/S cell cycle block, and this block can be partially relieved by depleting Elg1. Furthermore, depletion of Enok reduced the chromatin-bound levels of PCNA in both S2 cells and early embryos, suggesting that the Enok complex may interact with the Elg1 complex and down-regulate its PCNA-unloading function to promote the G1/S transition. Supporting this hypothesis, depletion of Enok also partially rescued the endoreplication defects in Elg1-depleted nurse cells. Taken together, our study provides novel insights into the roles of KAT6 HATs in cell cycle regulation through modulating PCNA levels on chromatin.

Indexed as

AnimalsCell Cycle CheckpointsCells, CulturedChromatinDown-RegulationDrosophila melanogasterDrosophila ProteinsFemaleG1 Phase Cell Cycle CheckpointsHistone AcetyltransferasesProliferating Cell Nuclear AntigenProtein BindingProtein SubunitsChromatinDrosophila ProteinsElg1 protein, DrosophilaEnok protein, DrosophilaHistone AcetyltransferasesProliferating Cell Nuclear AntigenProtein Subunitscell cycle progressionchromatinhistone acetyltransferasePCNA unloading

Identifiers

PMID27198229
PMCPMC4888840
OpenAlexW2395152483

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.