The ataxia-telangiectasia gene product, a constitutively expressed nuclear protein that is not up-regulated following genome damage

被引:137
作者
Brown, KD
Ziv, Y
Sadanandan, SN
Chessa, L
Collins, FS
Shiloh, Y
Tagle, DA
机构
[1] NATL HUMAN GENOME RES INST, NIH, LAB GENE TRANSFER, BETHESDA, MD 20892 USA
[2] TEL AVIV UNIV, SACKLER SCH MED, DEPT HUMAN GENET, IL-69978 RAMAT AVIV, ISRAEL
[3] UNIV ROMA LA SAPIENZA, DIPARTIMENTO MED SPERIMENTALE, I-00161 ROME, ITALY
关键词
D O I
10.1073/pnas.94.5.1840
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The product of the ataxia-telangiectasia gene (ATM) was identified by using an antiserum developed to a peptide corresponding to the deduced amino acid sequence, The ATM protein is a single, high-molecular weight protein predominantly confined to the nucleus of human fibroblasts, but is present in both nuclear and microsomal fractions from human lymphoblast cells and peripheral blood lymphocytes, ATM protein levels and localization remain constant throughout all stages of the cell cycle, Truncated ATM protein was not detected in lymphoblasts from ataxia-telangiectasia patients homozygous for mutations leading to premature protein termination, Exposure of normal human cells to gamma-irradiation and the radiomimetic drug neocarzinostatin had no effect on ATR;I protein levels, in contrast to a noted rise in p53 levels over the same time interval, These findings are consistent with a role for the ATM protein in ensuring the fidelity of DNA repair and cell cycle regulation following genome damage.
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页码:1840 / 1845
页数:6
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