Paradoxes in longevity:: sequence analysis of mtDNA haplogroup J in centenarians

被引:93
作者
Rose, G
Passarino, G
Carrieri, G
Altomare, K
Greco, V
Bertolini, S
Bonafè, M
Franceschi, C
De Benedictis, G [1 ]
机构
[1] Univ Calabria, Dept Cell Biol, I-87030 Arcavacata Di Rende, Italy
[2] Univ Genoa, Dept Internal Med, Genoa, Italy
[3] Univ Bologna, Dept Expt Pathol, I-40126 Bologna, Italy
[4] Natl Inst Aging Res, Ancona, Italy
关键词
aging; longevity; mitochondrial DNA;
D O I
10.1038/sj.ejhg.5200703
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Previous studies have shown that mitochondrial DNA (mtDNA) haplogroup J is significantly over-represented in healthy centenarians with respect to younger controls, thus suggesting that this haplogroup predisposes to successful aging and longevity. On the other hand, the same haplogroup is reported to have elevated frequency in some complex diseases. To verify if centenarians clustered in a particular lineage within J we have sequenced the D-loop region from 18 centenarians and 18 younger controls, previously characterized to be J. Then the entire mtDNA molecule was sequenced in a sub-sample of nine centenarians to find possible functional mutations associated with haplogroup J in successful aging. No clustering of the J haplogroup mtDNA from centenarians was observed. In addition, most of the mutations found are known as disease-associated mutations. The general picture that emerges from the study is that the J haplogroup of centenarians is surprisingly similar to that found in complex diseases, as well as in Leber Hereditary Optic Neuropathy. This finding implies that the same mutations could predispose to disease or longevity, probably according to individual-specific genetic backgrounds and stochastic events. This data reveals another paradox of centenarians and confirms the complexity of the longevity trait.
引用
收藏
页码:701 / 707
页数:7
相关论文
共 42 条
[31]   mtDNA haplogroup J:: a contributing factor of optic neuritis [J].
Reynier, P ;
Penisson-Besnier, I ;
Moreau, C ;
Savagner, F ;
Vielle, B ;
Emile, J ;
Dubas, F ;
Malthièry, Y .
EUROPEAN JOURNAL OF HUMAN GENETICS, 1999, 7 (03) :404-406
[32]   Phylogeography of mitochondrial DNA in western Europe [J].
Richards, MB ;
Macaulay, VA ;
Bandelt, HJ ;
Sykes, BC .
ANNALS OF HUMAN GENETICS, 1998, 62 :241-260
[33]  
ROBINE JM, 1999, PARADOXES LONGEVITY
[34]  
ROHLL A, 1997, MATH SEM U HAMB
[35]  
ROSS OA, 2001, IN PRESS EXP GERONTO
[36]   Human mtDNA haplogroups associated with high or reduced spermatozoa motility [J].
Ruiz-Pesini, E ;
Lapeña, AC ;
Díez-Sánchez, C ;
Pérez-Martos, A ;
Montoya, J ;
Alvarez, E ;
Díaz, M ;
Urriéis, A ;
Montoro, L ;
López-Pérez, MJ ;
Enríquez, JA .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (03) :682-696
[37]   Mitochondrial genotype associated with longevity [J].
Tanaka, M ;
Gong, JS ;
Zhang, J ;
Yoneda, M ;
Yagi, K .
LANCET, 1998, 351 (9097) :185-186
[38]  
Torroni A, 1997, AM J HUM GENET, V60, P1107
[39]   Mitochondrial DNA variation in human evolution and disease [J].
Wallace, DC ;
Brown, MD ;
Lott, MT .
GENE, 1999, 238 (01) :211-230
[40]   Mitochondrial diseases in man and mouse [J].
Wallace, DC .
SCIENCE, 1999, 283 (5407) :1482-1488