Ohnishi T, Nakamura O, Ozawa M, Arakaki N, Muramatsu T, Daikuhara Y
Department of Biochemistry, Kagoshima University Dental School, Sakuragaoka, Japan.
J Bone Miner Res. 1993 Mar;8(3):367-77. doi: 10.1002/jbmr.5650080314.
A complementary DNA (cDNA) for the 59 kD bone sialoprotein, which is supposed to be the rat counterpart of human alpha 2-HS glycoprotein (alpha 2-HSG) and is synthesized by both hepatocytes and osteoblasts, has been cloned from a rat liver cDNA library. Polyclonal rabbit antibodies to rat 59 kD bone sialoprotein were used to identify and isolate the cDNA. The amino acid sequence of 59 kD bone sialoprotein deduced from the cDNA revealed that the entire protein consisted of 352 amino acid residues, including a signal peptide of 18 amino acid residues, and contained three possible N-glycosylation sites. On Northern blot analysis of rat liver, an mRNA of about 1.5 kilobases was detected. An mRNA of 59 kD bone sialoprotein was also detectable in rat bone but not in other tissues, such as kidney, brain, and lung. A computer search of protein and nucleic acid data bases revealed that 68.2, 63.2, and 97.4% amino acid residues of 59 kD bone sialoprotein were identical with those of human alpha 2-HSG, bovine fetuin, and rat phosphorylated N-glycoprotein (pp63), respectively. The positions of cysteine residues in 59 kD bone sialoprotein also completely matched those in human alpha 2-HSG and bovine fetuin, indicating that the sialoprotein is the rat counterpart of human alpha 2-HSG and bovine fetuin. In addition, comparison of the nucleotide sequence of cDNA for rat fetuin/alpha 2-HSG with that for pp63 recently corrected showed only two differences in nucleotides in the entire protein coding regions of the two proteins, and immunoreactive rat fetuin/alpha 2-HSG in the conditioned medium of adult rat hepatocytes in primary culture was found to be phosphorylated. Thus, because rat fetuin/alpha 2-HSG isolated from bone and synthesized by osteoblasts in culture does not contain phosphorus, it seems to be pp63 dephosphorylated during circulation or in the bone matrix.
一种59kD骨唾液蛋白的互补DNA(cDNA)已从大鼠肝脏cDNA文库中克隆出来,该蛋白被认为是人类α2-HS糖蛋白(α2-HSG)的大鼠对应物,由肝细胞和成骨细胞共同合成。用针对大鼠59kD骨唾液蛋白的多克隆兔抗体来鉴定和分离该cDNA。从cDNA推导的59kD骨唾液蛋白的氨基酸序列显示,整个蛋白质由352个氨基酸残基组成,包括一个18个氨基酸残基的信号肽,并含有三个可能的N-糖基化位点。在对大鼠肝脏进行Northern印迹分析时,检测到一条约1.5千碱基的mRNA。在大鼠骨骼中也可检测到59kD骨唾液蛋白的mRNA,但在肾脏、大脑和肺等其他组织中未检测到。对蛋白质和核酸数据库进行计算机检索发现,59kD骨唾液蛋白的68.2%、63.2%和97.4%的氨基酸残基分别与人α2-HSG、牛胎球蛋白和大鼠磷酸化N-糖蛋白(pp63)的氨基酸残基相同。59kD骨唾液蛋白中半胱氨酸残基的位置也与人类α2-HSG和牛胎球蛋白中的完全匹配,表明该唾液蛋白是人类α2-HSG和牛胎球蛋白的大鼠对应物。此外,将大鼠胎球蛋白/α2-HSG的cDNA核苷酸序列与最近校正的pp63的核苷酸序列进行比较,发现在这两种蛋白质的整个蛋白质编码区中仅存在两个核苷酸差异,并且在原代培养的成年大鼠肝细胞的条件培养基中发现具有免疫反应性的大鼠胎球蛋白/α2-HSG被磷酸化。因此,由于从骨骼中分离并由培养的成骨细胞合成的大鼠胎球蛋白/α2-HSG不含磷,它似乎是在循环或骨基质中去磷酸化的pp63。