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GM01588 Fibroblast

Description:

ATAXIA-TELANGIECTASIA; AT

Affected:

Yes

Sex:

Male

Age:

No Data

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
  • External Links
  • Culture Protocols

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Hereditary Cancers
Chromosome Abnormalities
Class Repair Defective and Chromosomal Instability Syndromes
Class Syndromes with Increased Chromosome Breakage
Cell Type Fibroblast
Transformant Untransformed
Race White
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks 46,XY; clinically affected. Homozygous for ATM gene mutation ATM:c.103C>T (rs55861249); ARG35TER [mutation verified in GM01588 cell line by an external investigator].

Characterizations

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PDL at Freeze 4.1
Passage Frozen 15
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis and by Chromosome Analysis
 
REPAIR OF UV- OR X RAY-IRRADIATED DNA OR ALKYLATED DNA Bennett & Rainbow (Mutagenesis 3:389-395,1988) examined the UV-enhanced reactivation (UVER) and UV-enhanced mutagenesis (UVEM) of UVirradiated adenovirus in AT fibroblasts. UVER was examined using both V antigen expression as well as progeny production from infected cultures. Viral mutagenesis was studied by examining the induction of phenotypically wild-type revertants among the progeny obtained from fibroblasts infected with a temperature-sensitive early mutant of adenovirus (Ad5ts36). UVER factors for Ad V antigen expression were significantly less than normal in the AT strains tested when infection occurred immediately after UV-irradiation of cells. However, UVER factors were >1 and similar to those found for normal strains when cells were infected 24 h after UV-irradiation, indicating a delay in the expression of UVER for Ad V antigen in AT cells. UV-irradiation of both normal and AT cells 24 h prior to infection also resulted in a significant increase in progeny survival for UV-irradiated Ad. In normal cells, this progeny UVER was concomitant with a significant increase in the mutation frequency for UV-irradiated virus (increase in targeted mutagenesis) suggesting the existence of an inducible errorprone DNA repair mode in normal human cells. In contrast, pre-UV-irradiation of AT cells resulted in a significant decrease in the mutation frequency for UV-irradiated virus. These results suggest that AT cells lack an inducible error-prone DNA mode and that the delayed expression of UVER in AT cells results from a relatively error-free mechanism.
 
Gene ATM
Chromosomal Location 11q22.3
Allelic Variant 2 607585.0008; ATAXIA-TELANGIECTASIA
Identified Mutation ARG35TER; Gilad et al. [Hum. Molec. Genet. 5: 2033 (1996)] reported that a single AT mutation was observed in 32 of 33 defective ATM alleles in Jewish AT families of North African origin, coming from various regions of Morocco and Tunisia. This mutation, a 103C-T transition, results in a stop codon at position 35 of the ATM protein. No ATM protein could be detected in cells from patients with this mutation. Gilad et al. (1996) developed a rapid carrier detection assay for this mutation suitable for population-based screening.
 
Gene ATM
Chromosomal Location 11q22.3
Allelic Variant 8 607585.0008; ATAXIA-TELANGIECTASIA
Identified Mutation ARG35TER; Gilad et al. [Hum. Molec. Genet. 5: 2033 (1996)] reported that a single AT mutation was observed in 32 of 33 defective ATM alleles in Jewish AT families of North African origin, coming from various regions of Morocco and Tunisia. This mutation, a 103C-T transition, results in a stop codon at position 35 of the ATM protein. No ATM protein could be detected in cells from patients with this mutation. Gilad et al. (1996) developed a rapid carrier detection assay for this mutation suitable for population-based screening.

Phenotypic Data

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Remarks 46,XY; clinically affected. Homozygous for ATM gene mutation ATM:c.103C>T (rs55861249); ARG35TER [mutation verified in GM01588 cell line by an external investigator].

Publications

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Liu X, Hu M, Liu P, Jiao M, Zhou M, Lee AK, Li F, Li CY, ATM Paradoxically Promotes Oncogenic Transformation via Transcriptional Reprogramming Cancer research: 2020
PubMed ID: 32060145
 
O'Hagan HM, Ljungman M, Phosphorylation and nuclear accumulation are distinct events contributing to the activation of p53. Mutat Res546(1-2):7-15 2004
PubMed ID: 14757188
 
Alsbeih G, Brock WA, Terry N, Story MD, Analysis of radiation-induced DNA double-strand breaks misrepair is not compromized by broken DNA in human fibroblasts Radiation and environmental biophysics42:107-11 2003
PubMed ID: 12802598
 
Adamson AW, Kim WJ, Shangary S, Baskaran R, Brown KD, ATM is activated in response to N-methyl-N'-nitro-N-nitrosoguanidine-induced DNA alkylation. J Biol Chem277(41):38222-9 2002
PubMed ID: 12151394
 
Bennett CB, Rainbow AJ, Delayed expression of enhanced reactivation and decreased mutagenesis of UV-irradiated adenovirus in UV-irradiated ataxia telangiectasia fibroblasts. Mutagenesis3:389-95 1988
PubMed ID: 3070272
 
Hurt MM, Moses RE, Conversion of replicative intermediates in human DNA-repair defective cells. Exp Cell Res163:396-404 1986
PubMed ID: 3956584
 
Jeeves WP, Rainbow AJ, An aberration in gamma-ray-enhanced reactivation of irradiated adenovirus in ataxia telangiectasia fibroblasts. Carcinogenesis7:381-7 1986
PubMed ID: 3948323
 
Hurt MM, Beaudet AL, Moses RE, Stable low molecular weight DNA in xeroderma pigmentosum cells. Proc Natl Acad Sci U S A80:6987-91 1983
PubMed ID: 6196782
 
Huang, Genetic and biochemical studies with ataxia telangiectasia: A review. Hum Genet59:1-9 1981
PubMed ID: 10819014
 
Moses RE, Beaudet AL, Apurinic DNA endonuclease activities in repair-deficient human cell lines. Nucleic Acids Res5:463-73 1978
PubMed ID: 634794

External Links

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dbSNP dbSNP ID: 22381
NCBI GTR 208900 ATAXIA-TELANGIECTASIA; AT
OMIM 208900 ATAXIA-TELANGIECTASIA; AT
Omim Description AT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED
  AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED
  AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED
  AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED
  AT1
  ATAXIA-TELANGIECTASIA; AT
  LOUIS-BAR SYNDROMEATAXIA-TELANGIECTASIA MUTATED, INCLUDED; ATM, INCLUDED

Culture Protocols

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Passage Frozen 15
Split Ratio 1:4
Temperature 37 C
Percent CO2 5%
Percent O2 AMBIENT
Medium Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Not inactivated
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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