Trisomy 21 and accelerated aging: DNA-repair parameters in peripheral lymphocytes of Down's syndrome patients

被引:36
作者
Raji, NS [1 ]
Rao, KS [1 ]
机构
[1] Univ Hyderabad, Sch Life Sci, Dept Biochem, Hyderabad 500046, Andhra Pradesh, India
关键词
Down's syndrome; DNA-repair; unscheduled DNA synthesis; premature aging; DNA-polymerases; DNases;
D O I
10.1016/S0047-6374(97)00121-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Down's syndrome (DS) cases from 1-40 years of age and showing no other anomalies or deficiencies were categorized into three age groups: group 1, less than or equal to 12 years; group 2, 13-25 years; and group 3, greater than or equal to 26 years. The DNA-repair markers like unscheduled DNA synthesis (UDS), activities of DNA polymerases, (Total, beta and epsilon) and two endodeoxyribonucleases, (UV-and AP-DNases) were assessed in the peripheral lymphocytes of these subjects (under different conditions) along with age and sex matched normal healthy human subjects. The DS group showed lower DNA-repair efficiency and also an accelerated decline in DNA-repair capacity with age. These results indicate that deteriorated DNA-repair potential could be one of the probable reasons for premature aging seen in this chromosomal disorder. (C) 1998 Elsevier Science Ireland Ltd.
引用
收藏
页码:85 / 101
页数:17
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