Detection of the '4977 bp' mitochondrial DNA deletion in human atherosclerotic lesions

被引:39
作者
Bogliolo, M
Izzotti, A
De Flora, S
Carli, C
Abbondandolo, A
Degan, P
机构
[1] Univ Genoa, Inst Hyg & Prevent Med, I-16132 Genoa, Italy
[2] Ist Nazl Ric Canc, CSTA, Lab Mutagenesis, I-16132 Genoa, Italy
[3] Univ Genoa, Ctr Interuniv Ric Cancro, I-16132 Genoa, Italy
[4] Sampierdarena Hosp, Dept Pathol Anat, I-16149 Genoa, Italy
[5] Univ Genoa, Dept Clin & Expt Oncol, I-16132 Genoa, Italy
关键词
D O I
10.1093/mutage/14.1.77
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The presence of the 4977 bp deletion ('common deletion') in the mitochondrial DNA (mtDNA) is associated with defects in the metabolic machinery acquired during ageing as a hallmark of a degenerative phenotype, We analysed 27 samples (18 from surgical patients and nine from autopsy cases) of DNA extracted from smooth muscle cells of abdominal aorta fragments affected by atherosclerotic lesions. The deletion was detected by PCR amplification-gel electrophoresis and characterized by sequencing of the PCR product. The mtDNA 'common deletion' was detected in all analysed samples. However, its levels were not particularly high, which may be ascribed to the fact that smooth muscle cells in atherosclerotic lesions have a lower energy requirement and an appreciable proliferation rate, as compared for instance with cardiac myocytes, When the subjects were divided into two numerically equivalent age classes (60-72 Sears plus a 45-year-old subject versus 73-95 years), the deletion had significantly higher levels in the older subjects. Conversely, its presence did not correlate with source (surgical or autoptic), sex, cigarettes consumption, other clinical and anamnestic parameters or with the levels of adducts and 8-hydroxy-2'-deoxyguanosine measured in the nuclear DNA of the same samples, A previously unreported deletion of 5111 bp was additionally found in the mtDNA from a 45-year-old woman. The origin of this lesion seems to be compatible with the slipped mispairing model proposed for the 'common deletion'.
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页码:77 / 82
页数:6
相关论文
共 26 条
[21]   THE PATHOGENESIS OF ATHEROSCLEROSIS - A PERSPECTIVE FOR THE 1990S [J].
ROSS, R .
NATURE, 1993, 362 (6423) :801-809
[22]   SPECTRUM OF MITOCHONDRIAL-DNA REARRANGEMENTS IN THE PEARSON MARROW-PANCREAS SYNDROME [J].
ROTIG, A ;
BOURGERON, T ;
CHRETIEN, D ;
RUSTIN, P ;
MUNNICH, A .
HUMAN MOLECULAR GENETICS, 1995, 4 (08) :1327-1330
[23]   A DIRECT REPEAT IS A HOTSPOT FOR LARGE-SCALE DELETION OF HUMAN MITOCHONDRIAL-DNA [J].
SCHON, EA ;
RIZZUTO, R ;
MORAES, CT ;
NAKASE, H ;
ZEVIANI, M ;
DIMAURO, S .
SCIENCE, 1989, 244 (4902) :346-349
[24]   DISEASES OF THE MITOCHONDRIAL-DNA [J].
WALLACE, DC .
ANNUAL REVIEW OF BIOCHEMISTRY, 1992, 61 :1175-1212
[25]   THE OXIDATION HYPOTHESIS OF ATHEROSCLEROSIS [J].
WITZTUM, JL .
LANCET, 1994, 344 (8925) :793-795
[26]  
ZEVIANI M, 1988, NEUROLOGY, V38, P1339