CaMKII oxidation is a critical performance/disease trade-off acquired at the dawn of vertebrate evolution

CaMKII氧化是脊椎动物进化初期获得的一种关键的性能/疾病权衡。

阅读:4
作者:Qinchuan Wang ,Erick O Hernández-Ochoa ,Meera C Viswanathan ,Ian D Blum ,Danh C Do ,Jonathan M Granger ,Kevin R Murphy ,An-Chi Wei ,Susan Aja ,Naili Liu ,Corina M Antonescu ,Liliana D Florea ,C Conover Talbot Jr ,David Mohr ,Kathryn R Wagner ,Sergi Regot ,Richard M Lovering ,Peisong Gao ,Mario A Bianchet ,Mark N Wu ,Anthony Cammarato ,Martin F Schneider ,Gabriel S Bever ,Mark E Anderson

Abstract

Antagonistic pleiotropy is a foundational theory that predicts aging-related diseases are the result of evolved genetic traits conferring advantages early in life. Here we examine CaMKII, a pluripotent signaling molecule that contributes to common aging-related diseases, and find that its activation by reactive oxygen species (ROS) was acquired more than half-a-billion years ago along the vertebrate stem lineage. Functional experiments using genetically engineered mice and flies reveal ancestral vertebrates were poised to benefit from the union of ROS and CaMKII, which conferred physiological advantage by allowing ROS to increase intracellular Ca2+ and activate transcriptional programs important for exercise and immunity. Enhanced sensitivity to the adverse effects of ROS in diseases and aging is thus a trade-off for positive traits that facilitated the early and continued evolutionary success of vertebrates.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。