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机构地区:[1]湖南医科大学组织学与胚胎学教研室,湖南省畜牧研究所,湖南省委行政处奶牛场
出 处:《湖南医科大学学报》1995年第2期176-178,共3页Bulletin of Hunan Medical University
基 金:国家自然科学基金
摘 要:采用改良的蛋白酶消化方法,选择新鲜或冷冻牛精液,经Q-M染色法检测牛精子F小体。结果发现:酶消化处理后随着染色时间延长(30min,60min,120min),F小体检测率递增(23.3±l.3,43.2±1.6,46.6±1.0);而未经蛋白酶处理者,F小体的检测率很低。资料表明,在牛部分精子头部能检测到F小体,可能与酶对精子膜的消化有关。消化后质膜对染料的通透性增高,高度螺旋状态的DNA分子解聚,Y染色体上的显色基团得以暴露。n attenlpt was made to identify the fluorescent body (F-body )with qouinacrine mus-lard(Q-M) staining in the spermatozoa of bull. The fresh and frozen semen were stainedwith Q-M for l20min; the rates of F-body were only 2.2 ±1. 4 and 3. 4± l.6 respective-ly. Both kinds of specimens treated with lX protease and then stained for 30, 60, 120min,therates of F-body were 23.3±1.3,43. 2±1.6 and 46.6±1. 0 respectively, These results led tothe conclusion that the F-body is present in Y sperm of bull. The successful detection of Fbody in the sperm of bull is attributed to:(l) prolonged time of specimen in the Q-M solu-tion for staining,(2) the treatment to the membrane and depolymerization of aItitude spiralDNA by protease digestion which yielded more favorable condition for staining in the speci-mens.
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