Porcine dentin sialophosphoprotein - Length polymorphisms, glycosylation, phosphorylation, and stability

作者：Yamakoshi Yasuo; Lu Yuhe; Hu Jan C C; Kim Jung Wook; Iwata Takanori; Kobayashi Kazuyuki; Nagano Takatoshi; Yamakoshi Fumiko; Hu Yuanyuan; Fukae Makoto; Simmer James P^*

来源：Journal of Biological Chemistry, 2008, 283(21): 14835-14844.

DOI：10.1074/jbc.M800633200

Dentin sialophosphoprotein (DSPP) is critical for proper mineralization of tooth dentin, and mutations in DSPP cause inherited dentin defects. Dentin phosphoprotein (DPP) is the C-terminal cleavage product of DSPP that binds collagen and induces intrafibrillar mineralization. We isolated DPP from individual pigs and determined that its N-terminal and C-terminal domains are glycosylated and that DPP averages 155 phosphates per molecule. Porcine DPP is unstable at low pH and high temperatures, and complexing with collagen improves its stability. Surprisingly, we observed DPP size variations on SDS-PAGE for DPP isolated from individual pigs. These variations are not caused by differences in proteolytic processing or degrees of phosphorylation or glycosylation, but rather to allelic variations in Dspp. Characterization of the DPP coding region identified 4 allelic variants. Among the 4 alleles, 27 sequence variations were identified, including 16 length polymorphisms ranging from 3 to 63 nucleotides. None of the length variations shifted the reading frame, and all localized to the highly redundant region of the DPP code. The 4 alleles encode DPP domains having 551, 575, 589, or 594 amino acids and completely explain the DPP size variations. DPP length variations are polymorphic and are not associated with dentin defects.

• 出版日期2008-5-23