Mitochondrial DNA polymorphisms associated with longevity in a Finnish population

被引:213
作者
Niemi, AK
Hervonen, A
Hurme, M
Kurhunen, PJ
Jylhä, M
Majamaa, K
机构
[1] Oulu Univ, Dept Neurol, Oulu 90014, Finland
[2] Oulu Univ, Dept Med Biochem & Mol Biol, Oulu 90014, Finland
[3] Oulu Univ, Bioctr, Oulu 90014, Finland
[4] Tampere Univ, Sch Publ Hlth, Gerontol Lab, FIN-33101 Tampere, Finland
[5] Tampere Univ, Sch Med, Dept Microbiol & Immunol, FIN-33101 Tampere, Finland
[6] Tampere Univ, Sch Med, Dept Forens Med, FIN-33101 Tampere, Finland
[7] Tampere Univ Hosp, Ctr Lab Med, Tampere, Finland
基金
英国医学研究理事会; 芬兰科学院;
关键词
D O I
10.1007/s00439-002-0843-y
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Sequence variation in mitochondrial DNA (mtDNA) may cause slight differences both in the functioning of the respiratory chain and in free radical production, and an association between certain mtDNA haplogroups and longevity has been suggested. In order to determine further the role of mtDNA in longevity, we studied the frequencies of mtDNA haplogroups and haplogroup clusters among elderly subjects and controls in a Finnish population. Samples were obtained from 225 persons aged 90-91 years (Vitality 90+) and from 400 middle-aged controls and 257 infants. MtDNA haplogroups were determined by restriction fragment length polymorphism. The haplogroup frequencies of the Vitality 90+ group differed from both those of the middle-aged controls (P = 0.01) and the infants (P = 0.00005), haplogroup H being less frequent than among the middle-aged subjects (P = 0.001) and infants (P = 0.00001), whereas haplogroups U and J were more frequent. Haplogroup clusters also,differed between Vitality 90+ and both the middle-aged subjects (P = 0.002) and infants (P = 0.00001), the frequency of haplogroup cluster HV being lower in the former and that of UK and WIX being higher. These data suggest an association between certain mtDNA haplogroups or haplogroup clusters and longevity. Furthermore, our data appear to favour the presence of advantageous polymorphisms and support a role for mitochondria and mtDNA in the degenerative processes involved in ageing.
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页码:29 / 33
页数:5
相关论文
共 35 条
[1]   FAMILIAL COMPONENT IN LONGEVITY - STUDY OF OFFSPRING OF NONAGENARIANS .3. INTRAFAMILIAL STUDIES [J].
ABBOTT, MH ;
ABBEY, H ;
BOLLING, DR ;
MURPHY, EA .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1978, 2 (02) :105-120
[2]   FAMILY PATTERNS OF CORONARY HEART-DISEASE MORTALITY - THE FRAMINGHAM LONGEVITY STUDY [J].
BRAND, FN ;
KIELY, DK ;
KANNEL, WB ;
MYERS, RH .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 1992, 45 (02) :169-174
[3]  
Brown MD, 1997, AM J HUM GENET, V60, P381
[4]   Mitochondrial DNA inherited variants are associated with successful aging and longevity in humans [J].
De Benedictis, G ;
Rose, G ;
Carrieri, G ;
De Luca, M ;
Falcone, E ;
Passarino, G ;
Bonafé, M ;
Monti, D ;
Baggio, G ;
Bertolini, S ;
Mari, D ;
Mattace, R ;
Franceschi, C .
FASEB JOURNAL, 1999, 13 (12) :1532-1536
[5]  
De Benedictis G, 2000, ANN NY ACAD SCI, V908, P208
[6]  
Excoffier, 2000, ARLEQUIN VERSION 2 0
[7]   Phylogenetic network for European mtDNA [J].
Finnilä, S ;
Lehtonen, MS ;
Majamaa, K .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (06) :1475-1484
[8]   Phylogenetic network of the mtDNA haplogroup U in northern Finland based on sequence analysis of the complete coding region by conformation-sensitive gel electrophoresis [J].
Finnilä, S ;
Hassinen, IE ;
Ala-Kokko, L ;
Majamaa, K .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (03) :1017-1026
[9]   Does nonneutral evolution shape observed patterns of DNA variation in animal mitochondrial genomes? [J].
Gerber, AS ;
Loggins, R ;
Kumar, S ;
Dowling, TE .
ANNUAL REVIEW OF GENETICS, 2001, 35 :539-566
[10]   Mitochondrial DNA mutations, oxidative stress, and aging [J].
Golden, TR ;
Melov, S .
MECHANISMS OF AGEING AND DEVELOPMENT, 2001, 122 (14) :1577-1589