With the consensus sequence information of the serum glucocorticoid-induced protein kinase-1 (SGK1) phosphorylation site {R-X-R-X-X-(S/T)φ where φ is any hydrophobic amino acid}, we noticed that the transient receptor potential vanilloid 4 (TRPV4) cation channel, a member of the TRP vanilloid subfamily, harbors the putative SGK1 phosphorylation site (on its Ser 824). We have demonstrated that TRPV4 is an SGK1 authentic substrate protein, with the phosphorylation on the Ser 824 of TRPV4 by SGK1. Further, using TRPV4 mutants (S824A and S824D), we noted that the modification of the Ser 824 activates its Ca2+ entry, and sensitizes the TRPV4 channel to 4-α-phorbol 12,13-didecanoate (4-αPDD) or heat, simultaneously enhancing its active state. Additionally, we determined that the modification of the Ser 824 controls both its plasma membrane localization and its protein interactions with calmodulin. Thus, we have proposed herein that phosphorylation on the Ser 824 of TRPV4 is one of the control points for the regulation of its functions. © 2010 Korean Society for Integrative Biology.
CITATION STYLE
Lee, E. J., Shin, S. H., Chun, J., Hyun, S., Kim, Y., & Kang, S. S. (2010). The modulation of TRPV4 channel activity through its Ser 824 residue phosphorylation by SGK1. Animal Cells and Systems, 14(2), 99–114. https://doi.org/10.1080/19768354.2010.486939
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