Determination of life-span in Caenorhabditis elegans by four clock genes

被引:408
作者
Lakowski, B [1 ]
Hekimi, S [1 ]
机构
[1] MCGILL UNIV,DEPT BIOL,MONTREAL,PQ H3A 1B1,CANADA
关键词
D O I
10.1126/science.272.5264.1010
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
The nematode worm Caenorhabditis elegans is a model system for the study of the genetic basis of aging. Maternal-effect mutations in four genes-clk-1, clk-2, clk-3, and gro-1-interact genetically to determine both the duration of development and life-span. Analysis of the phenotypes of these mutants suggests the existence of a general physiological clock in the worm. Mutations in certain genes involved in dauer formation (an alternative larval stage induced by adverse conditions in which development is arrested) can also extend life-span, but the life extension of Clock mutants appears to be independent of these genes. The daf-2(e1370) clk-1(e2519) worms, which carry life-span-extending mutations from two different pathways, live nearly five times as long as wild-type worms.
引用
收藏
页码:1010 / 1013
页数:4
相关论文
共 25 条
  • [1] [Anonymous], BIOL MECH AGING
  • [2] CROSSLINKAGE THEORY OF AGING
    BJORKSTEN, J
    [J]. JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 1968, 16 (04) : 408 - +
  • [3] COMFORT A, 1979, BIOL SENESCENCE
  • [4] DORMAN JB, 1995, GENETICS, V141, P1399
  • [5] FINCH DL, 1990, LONGEVITY SENESCENCE
  • [6] ROLE OF OXIDATIVE STRESS IN DROSOPHILA AGING
    FLEMING, JE
    REVEILLAUD, I
    NIEDZWIECKI, A
    [J]. MUTATION RESEARCH, 1992, 275 (3-6): : 267 - 279
  • [7] FRIEDMAN DB, 1988, GENETICS, V118, P75
  • [8] AGING - A THEORY BASED ON FREE-RADICAL AND RADIATION-CHEMISTRY
    HARMAN, D
    [J]. JOURNALS OF GERONTOLOGY, 1956, 11 (03): : 298 - 300
  • [9] THE AGING PROCESS
    HARMAN, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (11): : 7124 - 7128
  • [10] HEKIMI S, 1995, GENETICS, V141, P1351