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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

机译:具有序列相似性成员20C的家族是骨中小整合素结合配体N连接糖蛋白的主要激酶但不是唯一的激酶

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摘要

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.
机译:最近的研究已将具有序列相似性成员20C(FAM20C)的家族鉴定为一种激酶,该激酶使与小整合素结合的配体N-连接糖蛋白(SIBLINGs)中的Ser-X-Glu / phospho-Ser(pSer)基序磷酸化Ser。没有体内证据可以证实这一发现,目前尚不清楚FAM20C是否是SIBLINGs的唯一激酶。我们从Fam20C基因敲除(KO)小鼠中提取了骨非胶原蛋白(NCPs),并分析了其磷酸化水平。通过阴离子交换色谱将总的NCPs分为骨桥蛋白,骨唾液蛋白和牙本质基质蛋白1富集的级分,并通过SDS-PAGE,天然PAGE和Western免疫印迹分析进行分析。 KO小鼠的NCP磷酸化水平低于野生型(WT)。在天然凝胶上,来自KO小鼠的SIBLINGs的迁移速率(Mr)比来自WT的更低。小牛肠磷酸酶处理将WT小鼠的SIBLINGs转移至与KO相邻的水平,但未能将后者转移,表明KO小鼠中SIBLINGs的磷酸化损失。质谱鉴定出来自KO小鼠[包括酸性富含Ser和天冬氨酸的基序(ASARM)肽区域]的SIBLING中较少的pSers。在一个有趣的发现中,KO小鼠的Ser-X-Glu基序中的几个pSers保持其磷酸化,而其他非Ser-X-Glu基序中的其他pSers则保持其磷酸化。 SIBLINGs中的磷酸-Tyrs和phospho-Thrs与FAM20C似乎无关。我们的结果表明,FAM20C是SIBLING的主要激酶,但不是唯一的激酶。-Yang,X.,Yan,W.,Tian,Y.,Ma,P.,Opperman,LA,Wang,X.序列相似性成员20C是骨中与小整合素结合的配体N-连接的糖蛋白的主要激酶,但不是唯一的激酶。

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