Colombatti A, Hughes E N, Taylor B A, August J T
Proc Natl Acad Sci U S A. 1982 Mar;79(6):1926-9. doi: 10.1073/pnas.79.6.1926.
A gene controlling the expression of a polymorphic 92,000-dalton glycoprotein of mouse macrophages and granulocytes has been identified. This glycoprotein was previously shown to be the major iodinated, trypsin-sensitive component of the murine phagocyte cell surface. The gene has been provisionally designated Pgp-1 for phagocyte glycoprotein 1. Expression of the glycoprotein was measured by monoclonal antibody binding to a polymorphic antigenic determinant. Antibody binding to cells of positive strains of mice was proportional to cell number, whereas binding to cells of negative strains was insignificant. The concentration of the antigen in cells of heterozygous mice was approximately 50% of that in homozygous mice. Thirteen of 33 recombinant inbred strains of mice were positive, with binding values 100-fold over background, suggesting that a single gene controlled expression of the antigen. Segregation of the antigen correlated with markers on chromosome 2. The segregation of Pgp-1, with nonagouti coat color (a) and hemolytic complement (Hc) activity among progeny of (C3H/HeJ x DBA/2J)F1 x DBA/2J mice confirmed the single gene control and the chromosomal assignment. Another gene on chromosome 2, Ly-m11, was also typed by using (BALB/cJ x C57BL/6J)F1 x C57BL/6J mice. The data from both of these crosses indicated the following gene order: Hc--Pgp-1--Ly-m11--a.
已鉴定出一个控制小鼠巨噬细胞和粒细胞中一种92,000道尔顿多态性糖蛋白表达的基因。此前已表明,这种糖蛋白是鼠吞噬细胞表面主要的碘化、对胰蛋白酶敏感的成分。该基因已被临时命名为Pgp-1,即吞噬细胞糖蛋白1。通过单克隆抗体与多态性抗原决定簇结合来测定糖蛋白的表达。抗体与阳性品系小鼠细胞的结合与细胞数量成正比,而与阴性品系细胞的结合不明显。杂合子小鼠细胞中抗原的浓度约为纯合子小鼠的50%。33个重组近交系小鼠中有13个呈阳性,结合值比背景高100倍,表明单个基因控制该抗原的表达。抗原的分离与2号染色体上的标记相关。在(C3H/HeJ×DBA/2J)F1×DBA/2J小鼠的后代中,Pgp-1与非阿高蒂毛色(a)和溶血补体(Hc)活性的分离证实了单基因控制和染色体定位。还利用(BALB/cJ×C57BL/6J)F1×C57BL/6J小鼠对2号染色体上的另一个基因Ly-m11进行了分型。这两个杂交实验的数据表明了以下基因顺序:Hc--Pgp-1--Ly-m11--a。