MITOCHONDRIAL-DNA DELETIONS IN HUMAN BRAIN - REGIONAL VARIABILITY AND INCREASE WITH ADVANCED AGE

被引:741
作者
CORRALDEBRINSKI, M
HORTON, T
LOTT, MT
SHOFFNER, JM
BEAL, MF
WALLACE, DC
机构
[1] EMORY UNIV,SCH MED,DEPT GENET & MOLEC MED,ATLANTA,GA 30322
[2] EMORY UNIV,SCH MED,DEPT NEUROL,ATLANTA,GA 30322
[3] MASSACHUSETTS GEN HOSP,DEPT NEUROL,BOSTON,MA 02114
[4] HARVARD UNIV,SCH MED,BOSTON,MA 02114
关键词
D O I
10.1038/ng1292-324
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We have examined the role of somatic mitochondrial DNA (mtDNA) mutations in human ageing by quantitating the accumulation of the common 4977 nucleotide pair (np) deletion (mtDNA4977) in the cortex, putamen and cerebellum. A significant increase in the mtDNA4977 deletion was seen in elderly individuals. In the cortex, the deleted to total mtDNA ratio ranged from 0.00023 to 0.012 in 67-77 year old brains and up to 0.034 in subjects over 80. In the putamen, the deletion level ranged from 0.0016 to 0.010 in 67 to 77 years old up to 0.12 in individuals over the age of 80. The cerebellum remained relatively devoid of mtDNA deletions. Similar changes were observed with a different 7436 np deletion. These changes suggest that somatic mtDNA deletions might contribute to the neurological impairment often associated with ageing.
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页码:324 / 329
页数:6
相关论文
共 40 条
[21]  
MIQUEL J, 1986, FREE RADICALS AGING, V51
[22]   THE CONSORTIUM TO ESTABLISH A REGISTRY FOR ALZHEIMERS-DISEASE (CERAD) .2. STANDARDIZATION OF THE NEUROPATHOLOGIC ASSESSMENT OF ALZHEIMERS-DISEASE [J].
MIRRA, SS ;
HEYMAN, A ;
MCKEEL, D ;
SUMI, SM ;
CRAIN, BJ ;
BROWNLEE, LM ;
VOGEL, FS ;
HUGHES, JP ;
VANBELLE, G ;
BERG, L .
NEUROLOGY, 1991, 41 (04) :479-486
[23]  
MORRIS JC, 1991, GERIATRICS, V46, P47
[24]   CYTOCHROME-C-OXIDASE DEFICIENT FIBERS IN THE LIMB MUSCLE AND DIAPHRAGM OF MAN WITHOUT MUSCULAR DISEASE - AN AGE-RELATED ALTERATION [J].
MULLERHOCKER, J .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1990, 100 (1-2) :14-21
[25]  
MULLERHOCKER J, 1989, AM J PATHOL, V134, P1167
[26]   MULTIPLE MITOCHONDRIAL-DNA DELETIONS EXIST IN CARDIOMYOCYTES OF PATIENTS WITH HYPERTROPHIC OR DILATED CARDIOMYOPATHY [J].
OZAWA, T ;
TANAKA, M ;
SUGIYAMA, S ;
HATTORI, K ;
ITO, T ;
OHNO, K ;
TAKAHASHI, A ;
SATO, W ;
TAKADA, G ;
MAYUMI, B ;
YAMAMOTO, K ;
ADACHI, K ;
KOGA, Y ;
TOSHIMA, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 170 (02) :830-836
[27]  
PARKER WD, 1992, ANN NY ACAD SCI, V640, P59
[28]   STUDIES OF SEQUENCE HETEROGENEITY OF MITOCHONDRIAL-DNA FROM RAT AND MOUSE-TISSUES - EVIDENCE FOR AN INCREASED FREQUENCY OF DELETIONS-ADDITIONS WITH AGING [J].
PIKO, L ;
HOUGHAM, AJ ;
BULPITT, KJ .
MECHANISMS OF AGEING AND DEVELOPMENT, 1988, 43 (03) :279-293
[29]   NORMAL OXIDATIVE DAMAGE TO MITOCHONDRIAL AND NUCLEAR-DNA IS EXTENSIVE [J].
RICHTER, C ;
PARK, JW ;
AMES, BN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (17) :6465-6467
[30]   SPONTANEOUS KEARNS-SAYRE CHRONIC EXTERNAL OPHTHALMOPLEGIA PLUS SYNDROME ASSOCIATED WITH A MITOCHONDRIAL-DNA DELETION - A SLIP REPLICATION MODEL AND METABOLIC THERAPY [J].
SHOFFNER, JM ;
LOTT, MT ;
VOLJAVEC, AS ;
SOUEIDAN, SA ;
COSTIGAN, DA ;
WALLACE, DC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (20) :7952-7956