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利用生物弹道式DNA递送技术在新型隐球菌中进行基因转移。

Gene transfer in Cryptococcus neoformans by use of biolistic delivery of DNA.

作者信息

Toffaletti D L, Rude T H, Johnston S A, Durack D T, Perfect J R

机构信息

Department of Medicine, Duke University Medical Center, Durham, North Carolina 27710.

出版信息

J Bacteriol. 1993 Mar;175(5):1405-11. doi: 10.1128/jb.175.5.1405-1411.1993.

Abstract

A transformation scheme for Cryptococcus neoformans to yield high-frequency, integrative events was developed. Adenine auxotrophs from a clinical isolate of C. neoformans serotype A were complemented by the cryptococcal phosphoribosylaminoimidazole carboxylase gene (ade2) with a biolistic DNA delivery system. Comparison of two DNA delivery systems (electroporation versus a biolistic system) showed notable differences. The biolistic system did not require linear vectors and transformed each auxotrophic strain at similar frequencies. Examination of randomly selected transformants by biolistics showed that 15 to 40% were stable, depending on the recipient auxotroph, with integrative events identified in all stable transformants by DNA analysis. Although the ade2 cDNA copy transformed at a low frequency, DNA analysis found homologous recombination in each of these transformants. DNA analysis of stable transformants receiving genomic ade2 revealed ectopic integration in a majority of cases, but approximately a quarter of the transformants showed homologous recombination with vector integration or gene replacement. This system has the potential for targeted gene disruption, and its efficiency will also allow for screening of DNA libraries within C. neoformans. Further molecular strategies to study the pathobiology of this pathogenic yeast are now possible with this transformation system.

摘要

开发了一种新型隐球菌的转化方案,以产生高频整合事件。利用生物弹道DNA递送系统,用新型隐球菌血清型A临床分离株的腺嘌呤营养缺陷型菌株与新型隐球菌磷酸核糖氨基咪唑羧化酶基因(ade2)进行互补。对两种DNA递送系统(电穿孔与生物弹道系统)的比较显示出显著差异。生物弹道系统不需要线性载体,并且以相似的频率转化每种营养缺陷型菌株。通过生物弹道法对随机选择的转化体进行检测表明,根据受体营养缺陷型的不同,15%至40%的转化体是稳定的,通过DNA分析在所有稳定转化体中都鉴定出了整合事件。虽然ade2 cDNA拷贝的转化频率较低,但DNA分析在这些转化体中的每一个中都发现了同源重组。对接受基因组ade2的稳定转化体进行DNA分析发现,在大多数情况下存在异位整合,但大约四分之一的转化体显示出与载体整合或基因替换的同源重组。该系统具有靶向基因破坏的潜力,其效率也将允许在新型隐球菌中筛选DNA文库。利用这种转化系统,现在有可能采取进一步的分子策略来研究这种致病酵母的病理生物学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3085/193227/16f229d4b0d5/jbacter00047-0209-a.jpg

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