Evidence map›Paper›PMID 19843163›Full record

ArticleThe FEBS journal2009

The nucleosome-binding protein HMGN2 modulates global genome repair.

Mangalam Subramanian, Rhiannon W Gonzalez, Hemangi Patil, Takahiro Ueda, Jae-Hwan Lim, Kenneth H Kraemer, Michael Bustin, Michael Bergel

Open access · greenAbstract read
In one paragraph

Article in The FEBS journal, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Biological Functions of HMGN Chromosomal Proteins.International journal of molecular sciences · 2020
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. [Inhibitory effects of high mobility group chromosomal protein N2 on human tongue carcinoma transplanted in nude mice].Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2014
    Article
  11. Article
  12. Article
  13. Article
  14. HMGNs, DNA repair and cancer.Biochimica et biophysica acta
    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

8 authors at 4 institutions in 3 countries.

Mangalam SubramanianDepartment of Biology, Texas Woman's University, Denton, TX 76204-5799, USA.
Rhiannon W Gonzalez
Hemangi Patil
Takahiro Ueda
Jae-Hwan Lim
Kenneth H Kraemer
Michael Bustin
Michael Bergel
Texas Woman's University · USNational Institutes of Health · USCenter for Cancer Research · USNational Cancer Institute · US

Funding

DNA Repair in Human Cancer-Prone Genetic DiseasesZIABC004517 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KRAEMER, KENNETH H · 2009 to 2024
$26.5M
Chromosomal Proteins and Chromosomal FunctionsZIABC004496 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI BUSTIN, MICHAEL · 2009 to 2023
$12.9M
Biological Functions of Chromosomal ProteinsZIABC011154 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI BUSTIN, MICHAEL · 2009 to 2023
$11.0M
Chromosomal Proteins and FunctionsZ01BC004496 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI BUSTIN, MICHAEL · 1997 to 2008
$3.0M
MBRS PROGRAM AT TEXAS WOMANS UNIVERSITYR25GM055380 · NIGMS · TEXAS WOMAN'S UNIVERSITY · PI UPHOUSE, LYNDA L · 1997 to 2008
$2.9M
DNA REPAIR IN HUMAN CANCER-PRONE GENETIC DISEASESZ01BC004517 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KRAEMER, KENNETH H · 1996 to 2008
$2.7M
Intramural NIH HHS Z01 BC004496Intramural NIH HHS Z01 BC004517Intramural NIH HHS ZIA BC004496NIGMS NIH HHS GM 55380NIGMS NIH HHS R25 GM055380
6 · The paper itself

Abstract

The HMGN family comprises nuclear proteins that bind to nucleosomes and alter the structure of chromatin. Here, we report that DT40 chicken cells lacking either HMGN2 or HMGN1a, or lacking both HMGN1a and HMGN2, are hypersensitive to killing by UV irradiation. Loss of both HMGN1a and HMGN2 or only HMGN2 increases the extent of UV-induced G(2)-M checkpoint arrest and the rate of apoptosis. HMGN null mutant cells showed slower removal of UV-induced DNA lesions from native chromatin, but the nucleotide excision repair remained intact, as measured by host cell reactivation assays. These results identify HMGN2 as a component of the global genome repair subpathway of the nucleotide excision repair pathway, and may indicate that HMGN2 facilitates the ability of the DNA repair proteins to access and repair UV-induced DNA lesions in chromatin. Our finding that HMGNs play a role in global DNA repair expands the role of these proteins in the maintenance of genome integrity.

Indexed as

DNA RepairAnimalsApoptosisBlotting, SouthwesternBlotting, WesternCell CycleCell SurvivalChickensChromatinGenomeHMGN1 ProteinHMGN2 ProteinUltraviolet RaysChromatinHMGN1 ProteinHMGN2 Protein

Identifiers

PMID19843163
PMCPMC3460546
OpenAlexW1595081529

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.