Yang Xiudong, Yan Wenjuan, Tian Ye, Ma Pan, Opperman Lynne A, Wang Xiaofang
*Department of Biomedical Sciences and Center for Craniofacial Research and Diagnosis, Texas A&M University Baylor College of Dentistry, Dallas, Texas, USA; Southern Medical University, Guangdong, People's Republic of China; Sichuan University, Sichuan, People's Republic of China; and Capital Medical University, Beijing, People's Republic of China.
*Department of Biomedical Sciences and Center for Craniofacial Research and Diagnosis, Texas A&M University Baylor College of Dentistry, Dallas, Texas, USA; Southern Medical University, Guangdong, People's Republic of China; Sichuan University, Sichuan, People's Republic of China; and Capital Medical University, Beijing, People's Republic of China
FASEB J. 2016 Jan;30(1):121-8. doi: 10.1096/fj.15-273607. Epub 2015 Aug 31.
Recent studies have identified family with sequence similarity member 20C (FAM20C) as a kinase that phosphorylates the Ser in Ser-X-Glu/phospho-Ser (pSer) motifs in the small-integrin-binding ligand N-linked glycoproteins (SIBLINGs). There is no in vivo evidence that validates this finding, and it is unclear whether FAM20C is the only kinase for SIBLINGs. We extracted bone noncollagenous proteins (NCPs) from Fam20C-knockout (KO) mice and analyzed the phosphorylation levels. The total NCPs were separated into osteopontin-, bone sialoprotein-, and dentin matrix protein-1-enriched fractions by anion-exchange chromatography and analyzed by SDS-PAGE, native PAGE, and Western immunoblot analysis. The NCP phosphorylation level in the KO mice was lower than that in the wild-type (WT). On the native gel, the SIBLINGs from KO mice showed a lower migration rate (Mr) than those from the WT. Calf intestine phosphatase treatment shifted SIBLINGs from the WT mice to the level adjacent to the KO, but failed to shift the latter, suggesting a phosphorylation loss of SIBLINGs in the KO mice. Mass spectrometry identified less pSers in the SIBLINGs from the KO mice [including the region of the acidic Ser- and aspartate-rich motif (ASARM) peptides]. In an intriguing finding, several pSers in the Ser-X-Glu motifs in the KO mice maintained their phosphorylation, whereas several others in non-Ser-X-Glu motifs did not. Phospho-Tyrs and phospho-Thrs in the SIBLINGs did not appear to be associated with FAM20C. Our results indicate that FAM20C is the primary, but not the only, kinase for the SIBLINGs.-Yang, X., Yan, W., Tian, Y., Ma, P., Opperman, L. A., Wang, X. Family with sequence similarity member 20C is the primary but not the only kinase for the small-integrin-binding ligand N-linked glycoproteins in bone.
最近的研究已确定序列相似性家族成员20C(FAM20C)是一种激酶,可磷酸化小整合素结合配体N-连接糖蛋白(SIBLINGs)中Ser-X-Glu/磷酸化丝氨酸(pSer)基序中的丝氨酸。目前尚无体内证据证实这一发现,并且尚不清楚FAM20C是否是SIBLINGs的唯一激酶。我们从Fam20C基因敲除(KO)小鼠中提取骨非胶原蛋白(NCPs)并分析其磷酸化水平。通过阴离子交换色谱法将总NCPs分离为富含骨桥蛋白、骨唾液蛋白和牙本质基质蛋白-1的组分,并通过SDS-PAGE、非变性PAGE和Western免疫印迹分析进行分析。KO小鼠中NCP的磷酸化水平低于野生型(WT)小鼠。在非变性凝胶上,KO小鼠的SIBLINGs迁移率(Mr)低于WT小鼠的。小牛肠磷酸酶处理使WT小鼠的SIBLINGs迁移至与KO小鼠相邻的水平,但未能使KO小鼠的SIBLINGs迁移,这表明KO小鼠中SIBLINGs的磷酸化缺失。质谱分析确定KO小鼠的SIBLINGs中磷酸化丝氨酸较少[包括富含酸性丝氨酸和天冬氨酸基序(ASARM)肽的区域]。一个有趣的发现是,KO小鼠中Ser-X-Glu基序中的几个磷酸化丝氨酸保持了其磷酸化状态,而非Ser-X-Glu基序中的其他几个磷酸化丝氨酸则没有。SIBLINGs中的磷酸化酪氨酸和磷酸化苏氨酸似乎与FAM20C无关。我们的结果表明,FAM20C是SIBLINGs的主要激酶,但不是唯一的激酶。-杨,X.,严,W.,田,Y.,马,P.,奥珀曼,L.A.,王,X.序列相似性家族成员20C是骨中小整合素结合配体N-连接糖蛋白的主要但非唯一激酶。