Arking R
Department of Biological Sciences, Wayne State University, Detroit, MI 48202.
Exp Aging Res. 1988 Summer-Autumn;14(2-3):125-35. doi: 10.1080/03610738808259737.
Genetic investigations into the aging processes of Drosophila have a long history. Much of the earlier work attempted the analysis of longevity in already existing and (usually) short-lived strains and mutants, but was unsuccessful because there was no way of assuring that the genes involved actually affected the normal aging processes. Success was achieved only when procedures were devised to specifically select for mutants and/or strains affecting the normal aging processes. Recent work has shown that the life span may be genetically altered either via an acceleration of the normal aging rate or via the stage-specific lengthening of certain portions of the adult life span. A variety of evidence suggests that aging is best viewed as a genetically determined, environmentally modulated, event dependent process. The evidence underlying these observations is discussed, a possible genetic model is presented and future directions are suggested.
对果蝇衰老过程的遗传学研究有着悠久的历史。早期的许多工作试图分析已有的(通常是)短命品系和突变体的寿命,但未获成功,因为无法确保所涉及的基因实际上影响了正常的衰老过程。只有当设计出专门选择影响正常衰老过程的突变体和/或品系的程序时,才取得了成功。最近的研究表明,寿命可能通过加速正常衰老速率或通过成年寿命某些部分的阶段特异性延长而在遗传上发生改变。各种证据表明,衰老最好被视为一个由基因决定、受环境调节的事件依赖性过程。本文讨论了这些观察结果的依据,提出了一个可能的遗传模型,并给出了未来的研究方向。