A genome-wide scan for linkage to human exceptional longevity identifies a locus on chromosome 4

被引:244
作者
Puca, AA
Daly, MJ
Brewster, SJ
Matise, TC
Barrett, J
Shea-Drinkwater, M
Kang, S
Joyce, E
Nicoli, J
Benson, E
Kunkel, LM
Perls, T
机构
[1] Harvard Univ, Sch Med, Boston, MA 02215 USA
[2] Childrens Hosp, Howard Hughes Med Inst, Div Genet, Boston, MA 02215 USA
[3] Harvard Univ, Sch Med, Div Aging, Boston, MA 02215 USA
[4] Beth Israel Deaconess Med Ctr, Biometr Ctr, Boston, MA 02215 USA
[5] Beth Israel Deaconess Med Ctr, Gerontol Div, Boston, MA 02215 USA
[6] Centagenetix, Boston, MA 02119 USA
[7] Rutgers State Univ, Dept Genet, Nelson Biol Labs, Piscataway, NJ 08854 USA
[8] Whitehead Inst Biomed Res, Ctr Genome Res, Cambridge, MA 02214 USA
关键词
D O I
10.1073/pnas.181337598
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Substantial evidence supports the familial aggregation of exceptional longevity. The existence of rare families demonstrating clustering for this phenotype suggests that a genetic etiology may be an important component. Previous attempts at localizing loci predisposing for exceptional longevity have been limited to association studies of candidate gene polymorphisms. In this study, a genome-wide scan for such predisposing loci was conducted by using 308 individuals belonging to 137 sibships demonstrating exceptional longevity. By using nonparametric analysis, significant evidence for linkage was noted for chromosome 4 at D4S1564 with a MLS of 3.65 (P = 0.044). The analysis was corroborated by a parametric analysis (P = 0.052). These linkage results indicate the likelihood that there exists a gene, or genes, that exerts a substantial influence on the ability to achieve exceptional old age. Identification of the genes in humans that allow certain individuals to live to extreme old age should lead to insights on cellular pathways that are important to the aging process.
引用
收藏
页码:10505 / 10508
页数:4
相关论文
共 17 条
  • [1] BELL F, 1997, COHORT LIFE TABLES
  • [2] Further evidence for the increased power of LOD scores compared with nonparametric methods
    Durner, M
    Vieland, VJ
    Greenberg, DA
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 64 (01) : 281 - 289
  • [3] Allegro, a new computer program for multipoint linkage analysis
    Gudbjartsson, DF
    Jonasson, K
    Frigge, ML
    Kong, A
    [J]. NATURE GENETICS, 2000, 25 (01) : 12 - 13
  • [4] Hadley EC, 2000, AM J EPIDEMIOL, V152, P1003
  • [5] Centenarians: the older you get, the healthier you have been
    Hitt, R
    Young-Xu, Y
    Silver, M
    Perls, T
    [J]. LANCET, 1999, 354 (9179) : 652 - 652
  • [6] Kruglyak L, 1996, AM J HUM GENET, V58, P1347
  • [7] GENETIC DISSECTION OF COMPLEX TRAITS - GUIDELINES FOR INTERPRETING AND REPORTING LINKAGE RESULTS
    LANDER, E
    KRUGLYAK, L
    [J]. NATURE GENETICS, 1995, 11 (03) : 241 - 247
  • [8] The efficiency of genetic analysis of DNA from aged siblings to detect chromosomal regions implicated in longevity
    Nemani, M
    Sahbatou, M
    Blanché, H
    Thomas, G
    Pascoe, L
    [J]. MECHANISMS OF AGEING AND DEVELOPMENT, 2000, 119 (1-2) : 25 - 39
  • [9] Exceptional familial clustering for extreme longevity in humans
    Perls, T
    Shea-Drinkwater, M
    Bowen-Flynn, J
    Ridge, SB
    Kang, S
    Joyce, E
    Daly, M
    Brewster, SJ
    Kunkel, L
    Puca, AA
    [J]. JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 2000, 48 (11) : 1483 - 1485
  • [10] Siblings of centenarians live longer
    Perls, TT
    Bubrick, E
    Wager, CG
    Vijg, J
    Kruglyak, L
    [J]. LANCET, 1998, 351 (9115) : 1560 - 1560