Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 1993 Mar;175(5):1405-11.
doi: 10.1128/jb.175.5.1405-1411.1993.

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

Affiliations
Comparative Study

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

D L Toffaletti et al. J Bacteriol. 1993 Mar.

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.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Cell. 1987 Dec 4;51(5):741-52 - PubMed
    1. Infect Immun. 1971 Feb;3(2):287-94 - PubMed
    1. Curr Genet. 1990 Feb;17(2):97-103 - PubMed
    1. Mol Cell Biol. 1990 Sep;10(9):4538-44 - PubMed
    1. Mycopathologia. 1982 Jul 23;79(1):23-9 - PubMed

Publication types

MeSH terms

Substances

LinkOut - more resources