Bedian V, Jungklaus C E
Department of Biology, Clarkson University, Potsdam, New York 13676.
Dev Genet. 1987;8(3):165-77. doi: 10.1002/dvg.1020080305.
The 63-kDa antigen recognized by the monoclonal antibody F7D6 is present in all Drosophila embryonic cells and disappears from most tissues as each one reaches its final, differentiated state. Larval tissues lose the antigen around the time of hatching, imaginal tissues lose it during metamorphosis, and germ cells lose it during gametogenesis (Bedian et al: Devel Biol 115:105-118, 1986). The nervous system and spontaneously contracting musculature of the gut and gonads are exceptions and remain antigen positive at all stages. The F7D6 antigen appears to be associated with dividing, undifferentiated cells and electrogenic cells. This prompted us to test tumors for antigen presence. We tested four different recessive mutants that give rise to four different types of tumorous transformation: the embryonic tumor Notch, several larval melanotic tumors, the imaginal disc tumor 1(2)gl, and three alleles of the ovarian tumor otu. In all cases, tumorous tissues in homozygotes contained the F7D6 antigen. The electrophoretic mobility of the antigen appeared to be unaltered in tumorous tissues compared to normal cells, but the antigen is expressed at higher levels. The antigen is found on the cytoplasmic surface of plasma membranes and appears to be a marker of undifferentiated normal and tumorous cells. Similarities and differences between the F7D6 antigen and Drosophila c-src protein are discussed.
单克隆抗体F7D6识别的63-kDa抗原存在于所有果蝇胚胎细胞中,随着每个组织达到其最终分化状态,该抗原会从大多数组织中消失。幼虫组织在孵化时左右失去该抗原,成虫盘组织在变态过程中失去它,生殖细胞在配子发生过程中失去它(贝迪安等人:《发育生物学》115:105 - 118,1986年)。神经系统以及肠道和性腺的自发收缩肌肉组织是例外,在所有阶段都保持抗原阳性。F7D6抗原似乎与正在分裂的未分化细胞和生电细胞有关。这促使我们检测肿瘤中是否存在该抗原。我们检测了四种不同的隐性突变体,它们会引发四种不同类型的肿瘤转化:胚胎肿瘤Notch、几种幼虫黑色素瘤、成虫盘肿瘤1(2)gl以及卵巢肿瘤otu的三个等位基因。在所有情况下,纯合子中的肿瘤组织都含有F7D6抗原。与正常细胞相比,肿瘤组织中该抗原的电泳迁移率似乎未改变,但抗原表达水平更高。该抗原存在于质膜的细胞质表面,似乎是未分化的正常细胞和肿瘤细胞的标志物。文中还讨论了F7D6抗原与果蝇c-src蛋白之间的异同。