Argon Yair, Gidalevitz Tali
Division of Cell Pathology, Department of Pathology and Lab Medicine, The Children's Hospital of Philadelphia and the University of Pennsylvania, 3615 Civic Center Blvd., 19104, Philadelphia, PA, USA,
Adv Exp Med Biol. 2015;847:45-72. doi: 10.1007/978-1-4939-2404-2_2.
Because aging is a multifactorial, pleiotropic process where many interacting mechanisms contribute to the organismal decline, the candidate gene approach rarely provides a clear message. This chapter discusses some of the inherent complexity, focusing on aspects that impinge upon protein homeostasis and maintain a healthy proteome. We discuss candidate genes that operate in these pathways, and compare their actions in invertebrates, mice and humans. We highlight several themes that emerge from recent research—the interconnections of pathways that regulate aging, the pleiotropic effects of mutations and other manipulations of the candidate proteins and the tissue specificity in these pleiotropic outcomes. This body of knowledge highlights the need for multiple specific readouts of manipulating longevity genes, beyond measuring lifespan, as well as the need to understand the integrated picture, beyond examining the immediate outputs of individual longevity pathways.
由于衰老过程是一个多因素、多效性的过程,其中许多相互作用的机制导致机体衰退,候选基因方法很少能给出明确的结论。本章将讨论一些内在的复杂性,重点关注影响蛋白质稳态并维持健康蛋白质组的方面。我们将讨论在这些途径中起作用的候选基因,并比较它们在无脊椎动物、小鼠和人类中的作用。我们强调了近期研究中出现的几个主题——调节衰老的途径之间的相互联系、候选蛋白质突变和其他操作的多效性影响以及这些多效性结果中的组织特异性。这一系列知识凸显了除测量寿命外,对操纵长寿基因进行多种特定读数的需求,以及除研究单个长寿途径的直接输出外,理解整体情况的必要性。