Longevity network: Construction and implications

被引:69
作者
Budovsky, Arie
Abramovich, Amir
Cohen, Raphael
Chalifa-Caspi, Vered
Fraifeld, Vadim
机构
[1] Ben Gurion Univ Negev, Fac Hlth Sci, Dept Microbiol & Immunol, Ctr Multidisciplinary Res Aging, IL-84105 Beer Sheva, Israel
[2] Ben Gurion Univ Negev, Natl Inst Biotechnol Negev, Bioinformat Support Unit, IL-84105 Beer Sheva, Israel
关键词
longevity genes and proteins; protein-protein interactions; longevity network; age-related diseases;
D O I
10.1016/j.mad.2006.11.018
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The vast majority of studies on longevity have focused on individual genes/proteins, without adequately addressing the possible role of interactions between them. This study is the first attempt towards constructing a "longevity network" via analysis of human protein-protein interactions (PPIs). For this purpose, we (i) compiled a complete list of established longevity genes from different species, including those that most probably affect the longevity in humans, (ii) defined the human orthologs of the longevity genes, and (iii) determined whether the encoded proteins could be organized as a network. The longevity gene-encoded proteins together with their interacting proteins form a continuous network, which fits the criteria for a scale-free network with an extremely high contribution of hubs to the network connectivity. Most of them have never been annotated before in connection with longevity. Remarkably, almost all of the hubs of the "longevity network" were reported to be involved in at least one age-related disease (ARD), with many being involved in several ARDs. This may be one of the ways by which the proteins with multiple interactions affect the longevity. The hubs offer the potential of being primary targets for longevity-promoting interventions. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:117 / 124
页数:8
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