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Alternative splicing modulates the frequency‐dependent response of CaMKII to Ca 2+ oscillations
Author(s) -
Bayer K. Ulrich,
Koninck Paul De,
Schulman Howard
Publication year - 2002
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1093/emboj/cdf360
Subject(s) - biology , alternative splicing , rna splicing , microbiology and biotechnology , genetics , exon , gene , rna
Ca 2+ oscillations are required in various signal trans duction pathways, and contain information both in their amplitude and frequency. Remarkably, the Ca 2+ /calmodulin(CaM)‐dependent protein kinase II (CaMKII) can decode such frequencies. A Ca 2+ /CaM‐stimulated autophosphorylation leads to Ca 2+ /CaM‐independent (autonomous) activity of the kinase that outlasts the initial stimulation. This autonomous activity increases exponentially with the frequency of Ca 2+ oscillations. Here we show that three β‐CaMKII splice variants (β M , β and β e ′) have very similar specific activity and maximal autonomy. However, their autonomy generated by Ca 2+ oscillations differs significantly. A mechanistic basis was found in alterations of the CaM activation constant and of the initial rate of autophosphorylation. Structurally, the splice variants differ only in a variable ‘linker’ region between the kinase and association domains. Therefore, we propose that differences in relative positioning of kinase domains within multimeric holoenzymes are responsible for the observed effects. Notably, the β‐CaMKII splice variants are differ entially expressed, even among individual hippocampal neurons. Taken together, our results suggest that alternative splicing provides cells with a mechanism to modulate their sensitivity to Ca 2+ oscillations.