CaMKII oxidation is a critical performance/disease trade-off acquired at the dawn of vertebrate evolution
Author
Wang, QinchuanHernández-Ochoa, Erick O
Viswanathan, Meera C
Blum, Ian D
Do, Danh C
Granger, Jonathan M
Murphy, Kevin R
Wei, An-Chi
Aja, Susan
Liu, Naili
Antonescu, Corina M
Florea, Liliana D
Talbot, C Conover
Mohr, David
Wagner, Kathryn R
Regot, Sergi
Lovering, Richard M
Gao, Peisong
Bianchet, Mario A
Wu, Mark N
Cammarato, Anthony
Schneider, Martin F
Bever, Gabriel S
Anderson, Mark E
Date
2021-05-26Journal
Nature CommunicationsPublisher
Springer NatureType
Article
Metadata
Show full item recordAbstract
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.Keyword
CaMKIIage-related disease
Calcium-Calmodulin-Dependent Protein Kinase Type 2
Evolution, Molecular
Reactive Oxygen Species--adverse effects
Identifier to cite or link to this item
http://hdl.handle.net/10713/15913ae974a485f413a2113503eed53cd6c53
10.1038/s41467-021-23549-3
Scopus Count
Collections
Related articles
- Hyperglycemia Acutely Increases Cytosolic Reactive Oxygen Species via O-linked GlcNAcylation and CaMKII Activation in Mouse Ventricular Myocytes.
- Authors: Lu S, Liao Z, Lu X, Katschinski DM, Mercola M, Chen J, Heller Brown J, Molkentin JD, Bossuyt J, Bers DM
- Issue date: 2020 May 8
- Reactive oxygen species-activated Ca/calmodulin kinase IIδ is required for late I(Na) augmentation leading to cellular Na and Ca overload.
- Authors: Wagner S, Ruff HM, Weber SL, Bellmann S, Sowa T, Schulte T, Anderson ME, Grandi E, Bers DM, Backs J, Belardinelli L, Maier LS
- Issue date: 2011 Mar 4
- Oxidized CaMKII (Ca(2+)/Calmodulin-Dependent Protein Kinase II) Is Essential for Ventricular Arrhythmia in a Mouse Model of Duchenne Muscular Dystrophy.
- Authors: Wang Q, Quick AP, Cao S, Reynolds J, Chiang DY, Beavers D, Li N, Wang G, Rodney GG, Anderson ME, Wehrens XHT
- Issue date: 2018 Apr
- Oxidative activation of the Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) regulates vascular smooth muscle migration and apoptosis.
- Authors: Zhu LJ, Klutho PJ, Scott JA, Xie L, Luczak ED, Dibbern ME, Prasad AM, Jaffer OA, Venema AN, Nguyen EK, Guan X, Anderson ME, Grumbach IM
- Issue date: 2014 Feb
- CaMKIIδ Met281/282 oxidation is not required for recovery of calcium transients during acidosis.
- Authors: Kreitmeier KG, Tarnowski D, Nanadikar MS, Baier MJ, Wagner S, Katschinski DM, Maier LS, Sag CM
- Issue date: 2021 Mar 1