Krøll J
Hafnia Unit of Biogerontology, Godthåbsvej 111,3, DK-2000, Frederiksberg, Denmark.
Biogerontology. 2005;6(5):357-61. doi: 10.1007/s10522-005-4809-z.
That evolution of longevity may depend on alterations in the expression of relatively few regulatory genes has been inferred from the rapid increase in lifespan during evolution of the hominid species (Cutler RG (1979) Mech Ageing Dev 9: 337-354). Also the inherent immortality of the embryonic stem cells implies that replicative senescence (Hayflick L (1997) Biochem Mosc 62: 1180-1190) as possibly aging of species are epigenetic phenomena. Evidence is presented to suggest that the epigenetic changes of the longevity determinants to a significant extend concerns the molecular chaperones. Specific involvement of RNA chaperones in cell immortalization and defective RecQ-DNA chaperones in syndromes of premature aging suggest that DNA/RNA - chaperones probably rank high among the determinants of cellular and species longevity.
人类物种进化过程中寿命的快速增长表明,寿命的进化可能取决于相对较少的调控基因表达的改变(Cutler RG (1979) Mech Ageing Dev 9: 337 - 354)。此外,胚胎干细胞固有的永生性意味着复制性衰老(Hayflick L (1997) Biochem Mosc 62: 1180 - 1190)以及物种衰老可能是表观遗传现象。有证据表明,寿命决定因素的表观遗传变化在很大程度上与分子伴侣有关。RNA伴侣在细胞永生化中的特定作用以及RecQ - DNA伴侣缺陷与早衰综合征的关系表明,DNA/RNA伴侣可能在细胞和物种寿命的决定因素中占据重要地位。