Evidence map›Paper›PMID 25077176›Full record

ArticleMolecular genetics & genomic medicine2014

A-TWinnipeg: Pathogenesis of rare ATM missense mutation c.6200C>A with decreased protein expression and downstream signaling, early-onset dystonia, cancer, and life-threatening radiotoxicity.

Kotoka Nakamura, Francesca Fike, Sara Haghayegh, Rachel Saunders-Pullman, Angelika J Dawson, Thilo Dörk, Richard A Gatti

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics & genomic medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Myoclonus-Dystonia Presentation ofMovement disorders clinical practice · 2022
    Article
  5. Review
  6. Article
  7. Article
  8. Article
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

7 authors at 4 institutions in 3 countries.

Kotoka NakamuraDepartment of Pathology and Laboratory Medicine, UCLA School of Medicine Los Angeles, California.
Francesca FikeDepartment of Pathology and Laboratory Medicine, UCLA School of Medicine Los Angeles, California.
Sara HaghayeghDepartment of Pathology and Laboratory Medicine, UCLA School of Medicine Los Angeles, California.
Rachel Saunders-PullmanDepartment of Neurology, Albert Einstein College of Medicine Bronx, New York.
Angelika J DawsonCytogenetics Laboratory, Division of Laboratory Medicine & Pathology, Departments of Biochemistry & Medical Genetics and Pediatrics & Child Health, Diagnostic Services of Manitoba, University of Manitoba Winnipeg, Manitoba, Canada.
Thilo DörkGynaecology Research Unit, Hannover Medical School Hannover, Germany.
Richard A GattiDepartment of Pathology and Laboratory Medicine, UCLA School of Medicine Los Angeles, California ; Department of Human Genetics, UCLA School of Medicine Los Angeles, California ; Molecular Biology Institute, UCLA Los Angeles, California.
University of California, Los Angeles · USAlbert Einstein College of Medicine · USMedizinische Hochschule Hannover · DEUniversity of Manitoba · CA

Funding

DRUG-INDUCED ATM READTHROUGH OF PTC MUTATIONSR01NS052528 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GATTI, RICHARD A · 2007 to 2011
$1.8M
Phenotypic Spectrum of LRRK2 MutationsK02NS073836 · NINDS · BETH ISRAEL MEDICAL CTR (NEW YORK) · PI SAUNDERS-PULLMAN, RACHEL · 2011 to 2015
$879k
NINDS NIH HHS K02 NS073836NINDS NIH HHS R01 NS052528
6 · The paper itself

Abstract

We studied 10 Mennonite patients who carry the c.6200C>A missense mutation (p.A2067D) in the ATM gene, all of whom exhibited a phenotypic variant of ataxia-telangiectasia (A-T) that is characterized by early-onset dystonia and late-onset mild ataxia, as previously described. This report provides the pathogenetic evidence for this mutation on cellular functions. Several patients have developed cancer and subsequently experienced life-threatening adverse reactions to radiation (radiotoxicity) and/or chemotherapy. As the c.6200C>A mutation is, thus far, unique to the Mennonite population and is always associated with the same haplotype or haplovariant, it was important to rule out any possible confounding DNA variant on the same haplotype. Lymphoblastoid cells derived from Mennonite patients expressed small amounts of ATM protein, which had no autophosphorylation activity at ATM Ser1981, and trace-to-absent transphosphorylation of downstream ATM targets. A-T lymphoblastoid cells stably transfected with ATM cDNA which had been mutated for c.6200C>A did not show a detectable amount of ATM protein. The same stable cell line with mutated ATM cDNA also showed a trace-to-absent transphosphorylation of downstream ATM targets SMC1pSer966 and KAP1pSer824. From these results, we conclude that c.6200A is the disease-causing ATM mutation on this haplotype. The presence of at least trace amounts of ATM kinase activity on some immunoblots may account for the late-onset, mild ataxia of these patients. The cause of the dystonia remains unclear. Because this dystonia-ataxia phenotype is often encountered in the Mennonite population in association with cancer and adverse reactions to chemotherapy, an early diagnosis is important.

Indexed as

AtaxiaATMcancer susceptibilitycDNA sequencingdystoniamissense mutationradiosensitivitytelangiectasia

Identifiers

PMID25077176
PMCPMC4113274
OpenAlexW2055808786

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Registered trials

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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.