Evidence map›Paper›PMID 27694478›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2017

Role of FEN1 S187 phosphorylation in counteracting oxygen-induced stress and regulating postnatal heart development.

Lina Zhou, Huifang Dai, Jian Wu, Mian Zhou, Hua Yuan, Juan Du, Lu Yang, Xiwei Wu, Hong Xu, Yuejin Hua and 3 more

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.2field-weighted citation impact, top 35% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

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  4. Observational
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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

13 authors at 5 institutions in 3 countries.

Lina ZhouCollege of Life Sciences and Institute of Nuclear-Agricultural Sciences, Zhejiang University, Hangzhou, China.
Huifang DaiDepartment of Cancer Genetics and Epigenetics and Beckman Research Institute of City of Hope, Duarte, California, USA.
Jian WuCenter for Craniofacial Molecular Biology, Herman Ostrow School of Dentistry, University of Southern California, Los Angeles, California, USA.
Mian ZhouDepartment of Cancer Genetics and Epigenetics and Beckman Research Institute of City of Hope, Duarte, California, USA.
Hua YuanDepartment of Diagnostic Ultrasound, Shaoxing Women and Children's Hospital, Shaoxing, China.
Juan DuDepartment of Cancer Genetics and Epigenetics and Beckman Research Institute of City of Hope, Duarte, California, USA.
Lu YangDepartment of Molecular and Cellular Biology, Beckman Research Institute of City of Hope, Duarte, California, USA; and.
Xiwei WuDepartment of Molecular and Cellular Biology, Beckman Research Institute of City of Hope, Duarte, California, USA; and.
Hong XuKey Laboratory of Chinese Ministry of Agriculture for Nuclear-Agricultural Sciences, Institute of Nuclear-Agricultural Sciences, Zhejiang University, Hangzhou, China.
Yuejin HuaKey Laboratory of Chinese Ministry of Agriculture for Nuclear-Agricultural Sciences, Institute of Nuclear-Agricultural Sciences, Zhejiang University, Hangzhou, China.
Jian XuCenter for Craniofacial Molecular Biology, Herman Ostrow School of Dentistry, University of Southern California, Los Angeles, California, USA.
Li ZhengDepartment of Cancer Genetics and Epigenetics and Beckman Research Institute of City of Hope, Duarte, California, USA; lzheng@coh.org.
Binghui ShenDepartment of Cancer Genetics and Epigenetics and Beckman Research Institute of City of Hope, Duarte, California, USA; bshen@coh.org.
Ministry of Agriculture · LVUniversity of Southern California · USBeckman Research InstituteCity Of Hope National Medical Center · USShaoxing City Women and Children Hospital · CN

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI STANLEY R. HAMILTON · 1985 to 2026
$86.3M
Function Analysis of FEN-1 Nuclease in Genome StabilityR01CA073764 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI BINGHUI SHEN · 2002 to 2026
$7.9M
Functional Analysis of Structure Specific Nucleases in Genome Stability and CancersR50CA211397 · NCI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI ZHENG, LI · 2016 to 2025
$3.3M
NCI NIH HHS P30 CA033572NCI NIH HHS R01 CA073764NCI NIH HHS R50 CA211397
6 · The paper itself

Abstract

Flap endonuclease 1 (FEN1) phosphorylation is proposed to regulate the action of FEN1 in DNA repair as well as Okazaki fragment maturation. However, the biologic significance of FEN1 phosphorylation in response to DNA damage remains unknown. Here, we report an in vivo role for FEN1 phosphorylation, using a mouse line carrying S187A FEN1, which abolishes FEN1 phosphorylation. Although S187A mouse embryonic fibroblast cells showed normal proliferation under low oxygen levels (2%), the mutant cells accumulated oxidative DNA damage, activated DNA damage checkpoints, and showed G

Indexed as

OxygenAmino Acid SequenceAnimalsDNA DamageFemaleFibroblastsFlap EndonucleasesG1 Phase Cell Cycle CheckpointsGene Expression Regulation, DevelopmentalHeartMaleMiceOxidative StressPhosphorylationPoint MutationFen1 protein, mouseFlap EndonucleasesOxygendilated heartflap endonuclease 1G1-phase arrestp53 signaling

Identifiers

PMID27694478
PMCPMC5161519
OpenAlexW2526619989

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.