Young M F, Bolander M E, Day A A, Ramis C I, Robey P G, Yamada Y, Termine J D
Nucleic Acids Res. 1986 Jun 11;14(11):4483-97. doi: 10.1093/nar/14.11.4483.
Overlapping cDNA clones encoding bovine osteonectin were isolated from a lambda gt11 expression library constructed from bovine bone cell mRNA. The longest clone, lambda On 17 (insert size 2.0 kb) was studied in detail. The clone was shown to encode osteonectin by hybrid select translation experiments and by DNA sequence analysis. Northern analysis of bone cell RNA showed the length of the osteonectin mRNA to be 2.0 kb. Osteonectin message was found in bone but not in soft tissue (liver and brain) preparations consistent with the distribution of the protein in these tissues. On the other hand, osteonectin message was observed in tendon, a tissue in which little or no osteonectin protein is found in vivo. Hybridization of osteonectin cDNA was detected in cells from a number of species including human, rat, mouse and chick. The level of osteonectin mRNA was drastically decreased in chick embryo fibroblasts transformed by Rous sarcoma virus.
从由牛骨细胞mRNA构建的λgt11表达文库中分离出编码牛骨连接蛋白的重叠cDNA克隆。对最长的克隆λOn 17(插入片段大小为2.0 kb)进行了详细研究。通过杂交选择翻译实验和DNA序列分析表明该克隆编码骨连接蛋白。对骨细胞RNA的Northern分析显示骨连接蛋白mRNA的长度为2.0 kb。在骨中发现了骨连接蛋白信息,但在软组织(肝脏和大脑)制剂中未发现,这与该蛋白质在这些组织中的分布一致。另一方面,在肌腱中观察到了骨连接蛋白信息,而在体内肌腱中发现很少或没有骨连接蛋白。在包括人、大鼠、小鼠和鸡在内的多种物种的细胞中检测到了骨连接蛋白cDNA的杂交。劳斯肉瘤病毒转化的鸡胚成纤维细胞中骨连接蛋白mRNA的水平急剧下降。