Dorman J B, Albinder B, Shroyer T, Kenyon C
Department of Biochemistry and Biophysics, University of California, San Francisco 94143-0554, USA.
Genetics. 1995 Dec;141(4):1399-406. doi: 10.1093/genetics/141.4.1399.
Recessive mutations in two genes, daf-2 and age-1, extend the lifespan of Caenorhabditis elegans significantly. The daf-2 gene also regulates formation of an alternative developmental state called the dauer. Here we asked whether these two genes function in the same or different lifespan pathways. We found that the longevity of both age-1 and daf-2 mutants requires the activities of the same two genes, daf-16 and daf-18. In addition, the daf-2(e1370); age-1(hx546) double mutant did not live significantly longer than the daf-2 single mutant. We also found that, like daf-2 mutations, the age-1(hx546) mutation affects certain aspects of dauer formation. These findings suggest that age-1 and daf-2 mutations do act in the same lifespan pathway and extend lifespan by triggering similar if not identical processes.
两个基因daf - 2和age - 1中的隐性突变显著延长了秀丽隐杆线虫的寿命。daf - 2基因还调控一种称为滞育的交替发育状态的形成。在此,我们探究这两个基因在相同还是不同的寿命途径中发挥作用。我们发现,age - 1和daf - 2突变体的长寿都需要相同的两个基因daf - 16和daf - 18的活性。此外,daf - 2(e1370); age - 1(hx546)双突变体的寿命并不比daf - 2单突变体显著延长。我们还发现,与daf - 2突变一样,age - 1(hx546)突变影响滞育形成的某些方面。这些发现表明,age - 1和daf - 2突变确实在相同的寿命途径中起作用,并通过触发相似(如果不是完全相同)的过程来延长寿命。