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The DNA and RNA polymerase genes of yeast plasmid pGKL2 are essential loci for plasmid integrity and maintenance

机译:酵母质粒pGK12的DNA和RNA聚合酶基因是质粒完整性和维护的必要基因座

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Summary: Novel recombinant plasmids derived from the Kluyveromyces lactis killer plasmid k2 have been constructed to study plasmid biology and gene function. In vivo recombination between native resident k2 and suitable disruption vectors, employing the KlTRP1 gene fused to a plasmid promoter as selection marker, yielded ORF2 and ORF6 deletion plasmids at high frequencies. As judged from Southern hybridization and plasmid restriction mapping analyses, these novel hybrids, termed rk2/2 and rk2/6, respectively, carry deletions in their putative DNA (ORF2) and RNA (ORF6) polymerase structural genes with central regions replaced by the input marker DNA. Long-term selection for TRP1 over 350 generations of growth did not favour maintenance of hybrids over wild-type k2. Thus, neither rk2/2 nor rk2/6 was fully functional and able to displace parental k2, indicating that both target genes are essential for plasmid integrity or maintenance. Recombinant plasmids were reduced in copy number relative to k2 with rk2/2 more drastically affected than rk2/6 implying a direct involvement of the ORF2 product in plasmid replication and an indirect maintenance function for the ORF6 gene product.
机译:发明内容:已经构建了衍生自Kluyveromyces乳酸乳裂杀伤质粒K2的新型重组质粒以研究质粒生物学和基因功能。在天然驻地K2和合适的破坏载体之间的体内重组中,使用熔融蛋白促进剂的KLTRP1基因作为选择标记,在高频下产生ORF2和ORF6缺失质粒。从Southern杂交和质粒限制映射分析中,这些新型杂交物分别称为RK2 / 2和RK2 / 6,在其推定的DNA(ORF2)和RNA(ORF6)聚合酶结构基因中携带缺失,其中中心区域被输入所取代的中心区域标记DNA。对于350多代生长超过350代的TRP1的长期选择不赞成在野生型K2上维持杂种。因此,RK2 / 2和RK2 / 6都不是完全官能的并且能够移位父母K2,表明靶基因两种靶基因对于质粒完整性或维护是必不可少的。在拷贝数中,相对于K2的拷贝数减少了重组质粒,其RK2 / 2比RK2 / 6更大的影响,暗示ORF2产物在质粒复制中直接涉及ORF6基因产物的间接维持功能。

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