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作 者:龚瑶琴[1] 陈丙玺[1] 郭辰虹[1] 刘晓军[1] 邹雅群[1]
机构地区:[1]山东医科大学医学遗传学教研室
出 处:《中华医学遗传学杂志》1999年第1期44-46,共3页Chinese Journal of Medical Genetics
基 金:卫生部优秀青年科技人才专项科研基金;山东省自然科学基金
摘 要:目的建立有效分离酵母人工染色体(yeastartificialchromosome,YAC)末端的方法。方法根据反向PCR原理,在分析YAC载体DNA序列的基础上,选用YAC载体上存在切点的限制性内切酶酶解YACDNA,通过连接反应形成环状DNA分子,再用与YAC载体两末端互补的引物进行扩增,扩增产物经进一步纯化后测序,即可得到YAC末端的序列。结果用反向PCR方法,分别从776E2、964C5、11D8和8D1共4个YAC分离得到各自的左右末端。结论该方法简便、有效。Objective To establish a highly efficient method for isolating yeast artificial chromosome(YAC) ends.Methods Based on the sequence of YAC vector, the frequent cutting enzymes were used to cleave within the vector and the genomic insert to generate relatively small fragments, which were ligated and subsequently amplified using vector primers that are in inverse orientation. The PCR products were purified and sequenced.Results 8 YAC termini were isolated from YAC 776E2, 964C5, 11D8 and 8D1.Conclusion The results suggest that inverse PCR be an efficient method for isolating YAC termini.
分 类 号:Q949.326.1[生物学—植物学] Q343.2
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