Ryan K A, Dasgupta S, Beverley S M
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115.
Gene. 1993 Sep 6;131(1):145-50. doi: 10.1016/0378-1119(93)90684-u.
We have developed two shuttle cosmid vectors for the trypanosomatid protozoan parasite Leishmania. Cosmids cLHYG and cLNEO contain hyg and neo markers, conferring resistance to hygromycin B and G418, respectively, replicate extrachromosomally after transfection into promastigotes, and bear a unique BamHI cloning site. To ensure the representation of telomeric sequences, which represent about 5% of the Leishmania genome, random insert DNAs were prepared by shearing followed by blunt-end ligation with BamHI adapters. Representative genomic libraries from Leishmania species representing the four major pathogenic complexes were prepared using cosmid cLHYG. The cosmid libraries were efficiently transfected into Leishmania, and individual cosmids were readily recovered by transformation back into Escherichia coli. The relatively small size of the Leishmania genome (50 Mb) combined with the capacity and transfection efficiency of these cosmid libraries (> 1000 Leishmania transfectants/plate) suggests the feasibility of functional genetic complementation in this parasite.
我们已经为锥虫原生动物寄生虫利什曼原虫开发了两种穿梭黏粒载体。黏粒cLHYG和cLNEO含有潮霉素B和新霉素抗性基因标记,分别赋予对潮霉素B和G418的抗性,转染到前鞭毛体后能在染色体外复制,并且带有一个独特的BamHI克隆位点。为了确保端粒序列(约占利什曼原虫基因组的5%)的代表性,通过剪切制备随机插入DNA,然后与BamHI衔接子进行平端连接。使用黏粒cLHYG制备了来自代表四种主要致病复合体的利什曼原虫物种的代表性基因组文库。这些黏粒文库被有效地转染到利什曼原虫中,并且通过再转化回大肠杆菌很容易回收单个黏粒。利什曼原虫基因组相对较小(50 Mb),再加上这些黏粒文库的容量和转染效率(>1000个利什曼原虫转染子/平板),表明在这种寄生虫中进行功能基因互补是可行的。