Evidence map›Paper›PMID 15743907›Full record

ArticleMolecular biology of the cell2005

ATRIP binding to replication protein A-single-stranded DNA promotes ATR-ATRIP localization but is dispensable for Chk1 phosphorylation.

Heather L Ball, Jeremy S Myers, David Cortez

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 153 papers.

0numbers the graph read from it
0cells of the map it votes in
153citing papers in PubMed
6.9field-weighted citation impact, top 2% 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

153 citing papers in PubMed, 238 citations in OpenAlex.

  1. Article
  2. Review
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  6. Cellular Senescence Triggered by Food and Environmental Genotoxins.International journal of molecular sciences · 2026
    Review
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  9. TheCancer management and research · 2026
    Review
  10. A NovelCurrent oncology (Toronto, Ont.) · 2025
    Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. Article

93 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

3 authors at 1 institution in 1 country.

Heather L BallDepartment of Biochemistry, Vanderbilt University, Nashville, TN 37232, USA.
Jeremy S Myers
David Cortez
Vanderbilt University · US

Funding

Structural Biology Facility CoreP30ES000267 · NIEHS · VANDERBILT UNIVERSITY · PI GUENGERICH, F PETER · 1985 to 2014
$20.3M
BIOCHEMICAL &CHEMICAL TRAINING FOR CANCER RESEARCHT32CA009582 · NCI · VANDERBILT UNIVERSITY · PI David K Cortez · 1987 to 2026
$8.8M
Function of the ATR-ATRIP ComplexR01CA102729 · NCI · VANDERBILT UNIVERSITY · PI CORTEZ, DAVID K · 2003 to 2018
$4.2M
TRAINING PROGRAM IN BREAST CANCER RESEARCHT32CA078136 · NCI · VANDERBILT UNIVERSITY · PI ARTEAGA, CARLOS L · 1998 to 2007
$2.4M
Signaling by the ATM and ATR KinasesK01CA093701 · NCI · VANDERBILT UNIVERSITY · PI CORTEZ, DAVID K · 2002 to 2006
$746k
NCI NIH HHS K01 CA093701NCI NIH HHS K01CA93701NCI NIH HHS R01 CA102729NCI NIH HHS R01CA102729NCI NIH HHS T32 CA009582NCI NIH HHS T32 CA078136NCI NIH HHS T32 CA78136NIEHS NIH HHS P30 ES000267NIEHS NIH HHS P30ES00267-38
6 · The paper itself

Abstract

ATR associates with the regulatory protein ATRIP that has been proposed to localize ATR to sites of DNA damage through an interaction with single-stranded DNA (ssDNA) coated with replication protein A (RPA). We tested this hypothesis and found that ATRIP is required for ATR accumulation at intranuclear foci induced by DNA damage. A domain at the N terminus of ATRIP is necessary and sufficient for interaction with RPA-ssDNA. Deletion of the ssDNA-RPA interaction domain of ATRIP greatly diminished accumulation of ATRIP into foci. However, the ATRIP-RPA-ssDNA interaction is not sufficient for ATRIP recognition of DNA damage. A splice variant of ATRIP that cannot bind to ATR revealed that ATR association is also essential for proper ATRIP localization. Furthermore, the ATRIP-RPA-ssDNA interaction is not absolutely essential for ATR activation because ATR phosphorylates Chk1 in cells expressing only a mutant of ATRIP that does not bind to RPA-ssDNA. These data suggest that binding to RPA-ssDNA is not the essential function of ATRIP in ATR-dependent checkpoint signaling and ATR has an important function in properly localizing the ATR-ATRIP complex.

Indexed as

Adaptor Proteins, Signal TransducingAtaxia Telangiectasia Mutated ProteinsBase SequenceBinding SitesCell Cycle ProteinsCell LineCell NucleusCheckpoint Kinase 1DNA-Binding ProteinsDNA DamageDNA, Single-StrandedExodeoxyribonucleasesHumansIn Vitro TechniquesPhosphoproteinsPhosphorylationAdaptor Proteins, Signal TransducingAtaxia Telangiectasia Mutated ProteinsATRIP protein, humanATR protein, humanCell Cycle ProteinsCheckpoint Kinase 1CHEK1 protein, humanDNA-Binding ProteinsDNA, Single-StrandedExodeoxyribonucleasesPhosphoproteinsProtein KinasesProtein Serine-Threonine KinasesReplication Protein ARNA, Small InterferingRPA1 protein, humanthree prime repair exonuclease 1

Identifiers

PMID15743907
PMCPMC1087242
OpenAlexW2125299927

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.