Evidence map›Paper›PMID 27264558›Full record

ReviewDNA repair2016

When DNA repair goes wrong: BER-generated DNA-protein crosslinks to oxidative lesions.

Jason Luis Quiñones, Bruce Demple

Open access · greenAbstract readReview
In one paragraph

Review in DNA repair, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 40 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

2 authors at 1 institution in 1 country.

Jason Luis QuiñonesStony Brook University School of Medicine, Department of Pharmacological Sciences, Stony Brook, NY, 11794, USA.
Bruce DempleStony Brook University School of Medicine, Department of Pharmacological Sciences, Stony Brook, NY, 11794, USA. Electronic address: bruce.demple@stonybrook.edu.
Stony Brook University · US

Funding

The Ape1-NPM1 Axis and Telomere MaintenanceR21CA191856 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI DEMPLE, BRUCE F. · 2016 to 2017
$374k
Single- and multinucleotide base excision DNA repair pathways in vivoR21CA198752 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI DEMPLE, BRUCE F. · 2015 to 2016
$374k
Formation and Fate of Oxidative DNA-Protein CrosslinksF31GM109747 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI QUINONES, JASON LUIS · 2014 to 2016
$90k
NCI NIH HHS R21 CA191856NCI NIH HHS R21 CA198752NIGMS NIH HHS F31 GM109747
6 · The paper itself

Abstract

Free radicals generate an array of DNA lesions affecting all parts of the molecule. The damage to deoxyribose receives less attention than base damage, even though the former accounts for ∼20% of the total. Oxidative deoxyribose fragments (e.g., 3'-phosphoglycolate esters) are removed by the Ape1 AP endonuclease and other enzymes in mammalian cells to enable DNA repair synthesis. Oxidized abasic sites are initially incised by Ape1, thus recruiting these lesions into base excision repair (BER) pathways. Lesions such as 2-deoxypentos-4-ulose can be removed by conventional (single-nucleotide) BER, which proceeds through a covalent Schiff base intermediate with DNA polymerase β (Polβ) that is resolved by hydrolysis. In contrast, the lesion 2-deoxyribonolactone (dL) must be processed by multinucleotide ("long-patch") BER: attempted repair via the single-nucleotide pathway leads to a dead-end, covalent complex with Polβ cross- linked to the DNA by an amide bond. We recently detected these stable DNA-protein crosslinks (DPC) between Polβ and dL in intact cells. The features of the DPC formation in vivo are exactly in keeping with the mechanistic properties seen in vitro: Polβ-DPC are formed by oxidative agents in line with their ability to form the dL lesion; they are not formed by non-oxidative agents; DPC formation absolutely requires the active-site lysine-72 that attacks the 5'-deoxyribose; and DPC formation depends on Ape1 to incise the dL lesion first. The Polβ-DPC are rapidly processed in vivo, the signal disappearing with a half-life of 15-30min in both mouse and human cells. This removal is blocked by inhibiting the proteasome, which leads to the accumulation of ubiquitin associated with the Polβ-DPC. While other proteins (e.g., topoisomerases) also form DPC under these conditions, 60-70% of the trapped ubiquitin depends on Polβ. The mechanism of ubiquitin targeting to Polβ-DPC, the subsequent processing of the expected 5'-peptidyl-dL, and the biological consequences of unrepaired DPC are important to assess. Many other lyase enzymes that attack dL can also be trapped in DPC, so the processing mechanisms may apply quite broadly.

Indexed as

DNA RepairAnimalsDeoxyriboseDNADNA-(Apurinic or Apyrimidinic Site) LyaseDNA DamageDNA Polymerase betaHalf-LifeHumansKetosesKineticsMiceOxidative StressProteasome Endopeptidase ComplexProtein BindingProteolysis2,4,5-trihydroxypentanoic acid gamma-lactoneAPEX1 protein, humanDeoxyriboseDNADNA-(Apurinic or Apyrimidinic Site) LyaseDNA Polymerase betaKetosesProteasome Endopeptidase ComplexSugar Acids2-deoxyribonolactoneAP lyaseBase excision DNA repairDNA polymerase βDNA-protein crosslinksOxidative DNA damage

Identifiers

PMID27264558
PMCPMC6420214
OpenAlexW2403797112

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.