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  • Secreted kinase phosphorylates extracellular proteins that regulate biomineralization.

Secreted kinase phosphorylates extracellular proteins that regulate biomineralization.

Science (New York, N.Y.) (2012-05-15)
Vincent S Tagliabracci, James L Engel, Jianzhong Wen, Sandra E Wiley, Carolyn A Worby, Lisa N Kinch, Junyu Xiao, Nick V Grishin, Jack E Dixon
ABSTRACT

Protein phosphorylation is a fundamental mechanism regulating nearly every aspect of cellular life. Several secreted proteins are phosphorylated, but the kinases responsible are unknown. We identified a family of atypical protein kinases that localize within the Golgi apparatus and are secreted. Fam20C appears to be the Golgi casein kinase that phosphorylates secretory pathway proteins within S-x-E motifs. Fam20C phosphorylates the caseins and several secreted proteins implicated in biomineralization, including the small integrin-binding ligand, N-linked glycoproteins (SIBLINGs). Consequently, mutations in Fam20C cause an osteosclerotic bone dysplasia in humans known as Raine syndrome. Fam20C is thus a protein kinase dedicated to the phosphorylation of extracellular proteins.