Evidence map›Paper›PMID 11157773›Full record

ArticleGenes & development2001

Domain structure, localization, and function of DNA polymerase eta, defective in xeroderma pigmentosum variant cells.

P Kannouche, B C Broughton, M Volker, F Hanaoka, L H Mullenders, A R Lehmann

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 127 papers.

0numbers the graph read from it
0cells of the map it votes in
127citing 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

127 citing papers in PubMed, 281 citations in OpenAlex.

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67 more citing papers are in PubMed but not listed here.

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 2 countries.

P KannoucheMRC Cell Mutation Unit, University of Sussex, Falmer, Brighton BN1 9RR, UK.
B C Broughton
M Volker
F Hanaoka
L H Mullenders
A R Lehmann
Leiden University Medical Center · NLUniversity of Sussex · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA polymerase eta carries out translesion synthesis past UV photoproducts and is deficient in xeroderma pigmentosum (XP) variants. We report that poleta is mostly localized uniformly in the nucleus but is associated with replication foci during S phase. Following treatment of cells with UV irradiation or carcinogens, it accumulates at replication foci stalled at DNA damage. The C-terminal third of poleta is not required for polymerase activity. However, the C-terminal 70 aa are needed for nuclear localization and a further 50 aa for relocalization into foci. Poleta truncations lacking these domains fail to correct the defects in XP-variant cells. Furthermore, we have identified mutations in two XP variant patients that leave the polymerase motifs intact but cause loss of the localization domains.

Indexed as

Amino Acid SequenceBase SequenceCell Line, TransformedCell NucleusDNADNA-Binding ProteinsDNA DamageDNA-Directed DNA PolymeraseDNA PrimersDNA RepairGenetic VariationGreen Fluorescent ProteinsHumansLuminescent ProteinsMolecular Sequence DataMutationDNADNA-Binding ProteinsDNA-Directed DNA PolymeraseDNA PrimersGreen Fluorescent ProteinsLuminescent ProteinsProliferating Cell Nuclear AntigenRad30 proteinRAD51 protein, humanRad51 RecombinaseRecombinant Fusion ProteinsY-Family DNA Polymerases

Identifiers

PMID11157773
PMCPMC312610
OpenAlexW2156419287

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.