Schibler L, Vaiman D, Oustry A, Guinec N, Dangy-Caye A L, Billault A, Cribiu E P
Département de Génétique Animale, INRA, Jouy-en-Josas, France.
Mamm Genome. 1998 Feb;9(2):119-24. doi: 10.1007/s003359900701.
A goat Bacterial Artificial Chromosome (BAC) library of 61,440 independent clones was constructed and characterized. The average size of the inserts was estimated at 153 kilobases by analyzing almost 500 clones using Not1 digestion followed by FIGE (Field Inverted Gel Electrophoresis) analysis. The library represents about three genome equivalents, which yields a theoretical probability of 0.95 of isolating a particular DNA sequence. After individual growth, the clones were arrayed in 40 superpools, which were organized in three dimension pools. A rapid technique for pool DNA preparation by microwave treatment was set up. This technique was compatible with PCR analysis. Primer pairs from 166 sequences (microsatellites, coding sequences from goat, and conserved Expressed Sequence Tags (ESTs) from humans) enabled the library to be successfully searched in 165 cases, with an average of 3.52 positive superpools. Only one sequence could not be found. The degree of chimerism was evaluated by FISH analysis with DNA from over 110 clones and was estimated at 4%. This BAC library will constitute an invaluable tool for positional cloning in ruminants, as well as for more general comparative mapping studies in mammals.
构建并表征了一个包含61,440个独立克隆的山羊细菌人工染色体(BAC)文库。通过使用Not1酶切,随后进行场反转凝胶电泳(FIGE)分析,对近500个克隆进行分析,估计插入片段的平均大小为153千碱基。该文库代表约三个基因组当量,分离特定DNA序列的理论概率为0.95。单个生长后,将克隆排列在40个超级池中,这些超级池被组织成三维池。建立了一种通过微波处理制备池DNA的快速技术。该技术与PCR分析兼容。来自166个序列(微卫星、山羊编码序列和人类保守表达序列标签(EST))的引物对使得在165个案例中成功搜索文库,平均有3.52个阳性超级池。只有一个序列未被找到。通过对110多个克隆的DNA进行荧光原位杂交(FISH)分析评估嵌合程度,估计为4%。这个BAC文库将成为反刍动物定位克隆以及哺乳动物更广泛的比较图谱研究的宝贵工具。