Regulation of brain-specific kinases 1 and 2 (BRSK1/2) by Ca2+/calmodulin

• BRSK1 and BRSK2 are identified as novel Ca 2+ /CaM-interacting kinases • Ca 2+ /CaM inhibits LKB1-catalyzed phosphorylation and activation of BRSK1/2 • Ca 2+ /CaM interacts with BRSK1 kinase domain to inhibit Thr189 phosphorylation • Ca 2+ /CaM interacts with phosphorylated BRSK1 without inhibiting its kinase activity We conducted a genome-wide calmodulin (CaM) interaction screening of 462 GST-fused human protein kinases to identify novel CaM-dependent protein kinases (CaMKs). In addition to known CaMKs, including myosin light chain kinases, CaMK2γ, and death-associated kinase 2, we identified the brain-specific protein kinase 2 (BRSK2, also known as SAD-A) as a novel CaM interactant. Proximity biotinylation and CaM–sepharose chromatography assays revealed that rat BRSK isoforms (BRSK1/2) interact with CaM in a Ca 2+ -dependent manner in vitro . We found that CaM suppresses the activation-loop phosphorylation of BRSK1 (at Thr189) and BRSK2 (at Thr175) by liver kinase B1 (LKB1), an activating kinase, in a Ca 2+ -dependent manner (IC 50 of ∼7 µM), thereby inhibiting BRSK activation. LKB1-catalyzed phosphorylation of the catalytic domain mutant of BRSK1 (residues 1–294) at Thr189 was suppressed by the addition of Ca 2+ /CaM, consistent with direct CaM binding of the kinase domain, as well as wild-type BRSK1. We confirmed that the LKB1 activity was not directly suppressed by Ca 2+ /CaM, supporting the hypothesis that the direct interaction of Ca 2+ /CaM with the kinase domain blocks the phosphorylation/activation of BRSK1/2 by LKB1. The kinase activity and PP2Cα-catalyzed dephosphorylation of LKB1-phosphorylated BRSK1 were not altered by Ca 2+ /CaM, although it was demonstrated to bind to Ca 2+ /CaM like that of unphosphorylated BRSK1. This unrecognized mechanism of BRSK1/2 regulation, involving the direct role of Ca 2+ /CaM binding, which inhibits phosphorylation/activation by LKB1, may open a new Ca 2+ signal transduction pathway in neurons.

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Journal
Cell Calcium
Published
2026-03-20
DOI
https://doi.org/10.1016/j.ceca.2026.103134
Primary Topic
Melanoma and MAPK Pathways
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article
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article

Regulation of brain-specific kinases 1 and 2 (BRSK1/2) by Ca2+/calmodulin

Ryo Morishita, Satomi Ohtsuka, Naoyuki Washida, Masaki Magari et al.
Cell Calcium
Melanoma and MAPK Pathways
article

Regulation of brain-specific kinases 1 and 2 (BRSK1/2) by Ca2+/calmodulin

Ryo Morishita, Satomi Ohtsuka, Naoyuki Washida, Masaki Magari, Haruki Yamauchi, Hiroshi Tokumitsu, Anna R. Brun, Moe Kataoka, Uryu Takezaki, Ko Hijikawa
article en

Abstract

• BRSK1 and BRSK2 are identified as novel Ca 2+ /CaM-interacting kinases • Ca 2+ /CaM inhibits LKB1-catalyzed phosphorylation and activation of BRSK1/2 • Ca 2+ /CaM interacts with BRSK1 kinase domain to inhibit Thr189 phosphorylation • Ca 2+ /CaM interacts with phosphorylated BRSK1 without inhibiting its kinase activity We conducted a genome-wide calmodulin (CaM) interaction screening of 462 GST-fused human protein kinases to identify novel CaM-dependent protein kinases (CaMKs). In addition to known CaMKs, including myosin light chain kinases, CaMK2γ, and death-associated kinase 2, we identified the brain-specific protein kinase 2 (BRSK2, also known as SAD-A) as a novel CaM interactant. Proximity biotinylation and CaM–sepharose chromatography assays revealed that rat BRSK isoforms (BRSK1/2) interact with CaM in a Ca 2+ -dependent manner in vitro . We found that CaM suppresses the activation-loop phosphorylation of BRSK1 (at Thr189) and BRSK2 (at Thr175) by liver kinase B1 (LKB1), an activating kinase, in a Ca 2+ -dependent manner (IC 50 of ∼7 µM), thereby inhibiting BRSK activation. LKB1-catalyzed phosphorylation of the catalytic domain mutant of BRSK1 (residues 1–294) at Thr189 was suppressed by the addition of Ca 2+ /CaM, consistent with direct CaM binding of the kinase domain, as well as wild-type BRSK1. We confirmed that the LKB1 activity was not directly suppressed by Ca 2+ /CaM, supporting the hypothesis that the direct interaction of Ca 2+ /CaM with the kinase domain blocks the phosphorylation/activation of BRSK1/2 by LKB1. The kinase activity and PP2Cα-catalyzed dephosphorylation of LKB1-phosphorylated BRSK1 were not altered by Ca 2+ /CaM, although it was demonstrated to bind to Ca 2+ /CaM like that of unphosphorylated BRSK1. This unrecognized mechanism of BRSK1/2 regulation, involving the direct role of Ca 2+ /CaM binding, which inhibits phosphorylation/activation by LKB1, may open a new Ca 2+ signal transduction pathway in neurons.

Cell CalciumVol. 135
Okayama University (JP), EM Strasbourg Business School (FR), CellFree Sciences (Japan) (JP), École Supérieure de Biotechnologie de Strasbourg (FR)
Zero hunger
Openalex Percentile: Top 14%
Melanoma and MAPK Pathways
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