Edman J C, Kwon-Chung K J
Hormone Research Institute, University of California, San Francisco 94143-0534.
Mol Cell Biol. 1990 Sep;10(9):4538-44. doi: 10.1128/mcb.10.9.4538-4544.1990.
A cDNA encoding Cryptococcus neoformans orotidine monophosphate pyrophosphorylase (OMPPase) has been isolated by complementation of the cognate Escherichia coli pyrE mutant. The cDNA was used as a probe to isolate a genomic DNA fragment encoding the OMPPase gene (URA5). By using electroporation for the introduction of plasmid DNA containing the URA5 gene, C. neoformans ura5 mutants could be transformed at low efficiency. Ura+ transformants obtained with supercoiled plasmids containing the URA5 gene showed marked mitotic instability and contained extrachromosomal URA5 sequences, suggesting limited ability to replicate within C. neoformans. Transformants obtained with linear DNA were of two classes: stable transformants with integrated URA5 sequences, and unstable transformants with extrachromosomal URA5 sequences.
通过对同源大肠杆菌pyrE突变体进行互补,分离出了编码新型隐球菌乳清苷单磷酸焦磷酸化酶(OMPPase)的cDNA。该cDNA用作探针,分离出编码OMPPase基因(URA5)的基因组DNA片段。通过电穿孔导入含有URA5基因的质粒DNA,新型隐球菌ura5突变体能够以低效率进行转化。用含有URA5基因的超螺旋质粒获得的Ura +转化体表现出明显的有丝分裂不稳定性,并含有染色体外URA5序列,这表明其在新型隐球菌内的复制能力有限。用线性DNA获得的转化体有两类:具有整合URA5序列的稳定转化体和具有染色体外URA5序列的不稳定转化体。