Uda Akihiko, Tanabayashi Kiyoshi, Mukai Ryozaburo, Terao Keiji, Yamada Akio
Tsukuba Primate Center for Medical Science, National Institute of Infectious Diseases, Ibaraki, Japan.
J Med Primatol. 2004 Feb;33(1):34-7. doi: 10.1111/j.1600-0684.2003.00047.x.
We previously reported that peripheral lymphocytes from about 12% of cynomolgus monkeys lacked reactivity with anti-rhesus monkey CD3 monoclonal antibody (FN18). The nucleotide sequence analysis of the genes encoding CD3 component proteins revealed that a single amino acid substitutions found in the CD3epsilon chain determined the phenotype. In this study, we attempted to develop a method based on the restriction fragment length polymorphism (RFLP) and apply it for determination of the genotypes of individual monkeys. Comparison of the phenotype determined by fluorescence-activated cell sorter analysis with the genotype determined by RFLP analysis revealed that the FN18 -positive trait was dominant over the FN18-negative trait. It was also revealed that allele frequency was significantly different among macaques depending on the geographical region where their ancestors were derived from.
我们之前报道过,约12%的食蟹猴外周淋巴细胞与抗恒河猴CD3单克隆抗体(FN18)缺乏反应性。对编码CD3组成蛋白的基因进行核苷酸序列分析发现,CD3ε链中单个氨基酸的替换决定了该表型。在本研究中,我们尝试开发一种基于限制性片段长度多态性(RFLP)的方法,并将其应用于个体猴子基因型的测定。通过荧光激活细胞分选分析确定的表型与通过RFLP分析确定的基因型进行比较,结果显示FN18阳性性状对FN18阴性性状呈显性。还发现,根据猕猴祖先来源的地理区域不同,其等位基因频率存在显著差异。