Quackenbush E, Clabby M, Gottesdiener K M, Barbosa J, Jones N H, Strominger J L, Speck S, Leiden J M
Proc Natl Acad Sci U S A. 1987 Sep;84(18):6526-30. doi: 10.1073/pnas.84.18.6526.
Complementary DNA (cDNA) clones encoding the heavy chain of the heterodimeric human membrane glycoprotein 4F2 have been isolated by immunoscreening of a lambda gt11 expression library. The identity of these clones has been confirmed by hybridization to RNA and DNA prepared from mouse L-cell transfectants, which were produced by whole cell gene transfer and selected for cell-surface expression of the human 4F2 heavy chain. DNA sequence analysis suggests that the 4F2 heavy-chain cDNAs encode an approximately 526-amino acid type II membrane glycoprotein, which is composed of a large C-terminal extracellular domain, a single potential transmembrane region, and a 50-81 amino acid N-terminal intracytoplasmic domain. Southern blotting experiments have shown that the 4F2 heavy-chain cDNAs are derived from a single-copy gene that has been highly conserved during mammalian evolution.
通过对λgt11表达文库进行免疫筛选,已分离出编码异二聚体人膜糖蛋白4F2重链的互补DNA(cDNA)克隆。这些克隆的身份已通过与从小鼠L细胞转染子制备的RNA和DNA杂交得到证实,这些转染子是通过全细胞基因转移产生的,并被选择用于人4F2重链的细胞表面表达。DNA序列分析表明,4F2重链cDNA编码一种约526个氨基酸的II型膜糖蛋白,它由一个大的C末端细胞外结构域、一个单一的潜在跨膜区域和一个50-81个氨基酸的N末端胞质内结构域组成。Southern印迹实验表明,4F2重链cDNA来自一个在哺乳动物进化过程中高度保守的单拷贝基因。