Evidence map›Paper›PMID 34083046›Full record

ReviewMutation research. Reviews in mutation research

Function and molecular mechanisms of APE2 in genome and epigenome integrity.

Yunfeng Lin, Anne McMahon, Garrett Driscoll, Sharon Bullock, Jianjun Zhao, Shan Yan

Open access · greenAbstract readReview
In one paragraph

Review in Mutation research. Reviews in mutation research. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

13 citing papers in PubMed, 21 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 2 institutions in 1 country.

Yunfeng LinDepartment of Biological Sciences, University of North Carolina at Charlotte, Charlotte, NC, 28223, United States.
Anne McMahonDepartment of Biological Sciences, University of North Carolina at Charlotte, Charlotte, NC, 28223, United States.
Garrett DriscollDepartment of Biological Sciences, University of North Carolina at Charlotte, Charlotte, NC, 28223, United States.
Sharon BullockDepartment of Biological Sciences, University of North Carolina at Charlotte, Charlotte, NC, 28223, United States.
Jianjun ZhaoDepartment of Cancer Biology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, 44195, United States.
Shan YanDepartment of Biological Sciences, University of North Carolina at Charlotte, Charlotte, NC, 28223, United States. Electronic address: shan.yan@uncc.edu.
University of North Carolina at Charlotte · USCleveland Clinic Lerner College of Medicine · US

Funding

Mechanism of APE1 in DNA damage responseR01CA225637 · NCI · UNIVERSITY OF NORTH CAROLINA CHARLOTTE · PI YAN, SHAN · 2018 to 2022
$1.9M
Role of APE2 in DNA damage responseR15GM114713 · NIGMS · UNIVERSITY OF NORTH CAROLINA CHARLOTTE · PI YAN, SHAN · 2015 to 2015
$363k
NCI NIH HHS R01 CA225637NIGMS NIH HHS R15 GM114713
6 · The paper itself

Abstract

APE2 is a rising vital player in the maintenance of genome and epigenome integrity. In the past several years, a series of studies have shown the critical roles and functions of APE2. We seek to provide the first comprehensive review on several aspects of APE2 in genome and epigenome integrity. We first summarize the distinct functional domains or motifs within APE2 including EEP (endonuclease/exonuclease/phosphatase) domain, PIP box and Zf-GRF motifs from eight species (i.e., Homo sapiens, Mus musculus, Xenopus laevis, Ciona intestinalis, Arabidopsis thaliana, Schizosaccharomyces pombe, Saccharomyces cerevisiae, and Trypanosoma cruzi). Then we analyze various APE2 nuclease activities and associated DNA substrates, including AP endonuclease, 3'-phosphodiesterase, 3'-phosphatase, and 3'-5' exonuclease activities. We also examine several APE2 interaction proteins, including PCNA, Chk1, APE1, Myh1, and homologous recombination (HR) factors such as Rad51, Rad52, BRCA1, BRCA2, and BARD1. Furthermore, we provide insights into the roles of APE2 in various DNA repair pathways (base excision repair, single-strand break repair, and double-strand break repair), DNA damage response (DDR) pathways (ATR-Chk1 and p53-dependent), immunoglobulin class switch recombination and somatic hypermutation, as well as active DNA demethylation. Lastly, we summarize critical functions of APE2 in growth, development, and diseases. In this review, we provide the first comprehensive perspective which dissects all aspects of the multiple-function protein APE2 in genome and epigenome integrity.

Indexed as

AnimalsArabidopsis ProteinsDNA DamageDNA DemethylationDNA RepairEndonucleasesEpigenomeHumansImmunityRad51 RecombinaseSaccharomyces cerevisiaeApe2 protein, ArabidopsisArabidopsis ProteinsATRAD51 protein, ArabidopsisEndonucleasesRad51 RecombinaseAPE2ATR-Chk1 pathwayDNA demethylationDNA repairGenome and epigenome integrityImmune response

Identifiers

PMID34083046
PMCPMC8287789
OpenAlexW3103060414

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.