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

Author:

Wang QinchuanORCID,Hernández-Ochoa Erick O.,Viswanathan Meera C.,Blum Ian D.ORCID,Do Danh C.,Granger Jonathan M.,Murphy Kevin R.ORCID,Wei An-Chi,Aja Susan,Liu Naili,Antonescu Corina M.,Florea Liliana D.ORCID,Talbot C. ConoverORCID,Mohr David,Wagner Kathryn R.,Regot SergiORCID,Lovering Richard M.,Gao PeisongORCID,Bianchet Mario A.ORCID,Wu Mark N.,Cammarato Anthony,Schneider Martin F.,Bever Gabriel S.,Anderson Mark E.ORCID

Abstract

AbstractAntagonistic 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.

Funder

U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute

U.S. Department of Health & Human Services | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

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