Xie Y, Muller W A
Laboratory of Cellular Physiology and Immunology, Rockefeller University, New York, NY 10021.
Proc Natl Acad Sci U S A. 1993 Jun 15;90(12):5569-73. doi: 10.1073/pnas.90.12.5569.
We describe the isolation and characterization of a functional murine platelet/endothelial cell adhesion molecule (PECAM) 1 cDNA clone from a mouse lung library. At the nucleotide level, the coding sequence of murine PECAM-1 is 73% identical to human PECAM-1, and at the amino acid level, the sequence is 79% homologous to its human counterpart. Southern hybridization reveals that one copy of the gene exists in the mouse genome; Northern hybridization reveals a single mRNA species in mouse lung tissue. COS-7 and mouse L cells transfected with murine PECAM-1 expressed a 130-kDa glycoprotein on their surfaces that reacted with anti-murine PECAM-1 monoclonal antibody and comigrated on SDS/PAGE with human PECAM-1. Stable L-cell transfectants aggregate with each other in a PECAM-dependent, homophilic manner.
我们描述了从小鼠肺文库中分离并鉴定功能性小鼠血小板/内皮细胞黏附分子(PECAM)1 cDNA克隆的过程。在核苷酸水平上,小鼠PECAM-1的编码序列与人类PECAM-1的一致性为73%;在氨基酸水平上,其序列与其人类对应物的同源性为79%。Southern杂交显示该基因在小鼠基因组中以单拷贝形式存在;Northern杂交显示在小鼠肺组织中存在单一的mRNA种类。用小鼠PECAM-1转染的COS-7细胞和小鼠L细胞在其表面表达一种130 kDa的糖蛋白,该糖蛋白与抗小鼠PECAM-1单克隆抗体发生反应,并在SDS/PAGE上与人PECAM-1共迁移。稳定的L细胞转染子以PECAM依赖的、同嗜性的方式相互聚集。