» Articles » PMID: 1573522

Selection of Ura5 and Ura3 Mutants from the Two Varieties of Cryptococcus Neoformans on 5-fluoroorotic Acid Medium

Overview
Journal J Med Vet Mycol
Specialty Microbiology
Date 1992 Jan 1
PMID 1573522
Citations 35
Authors
Affiliations
Soon will be listed here.
Abstract

Spontaneous mutants requiring uracil were isolated from both varieties of Cryptococcus neoformans by plating on 5-fluoroorotic acid (5-FOA) medium. Of the 36 strains tested (18 var. neoformans and 18 var. gattii), 24 (12 of each variety) generated 5-FOA-resistant cells requiring uracil for growth. Six of the 12 C. neoformans var. gattii strains produced ura3 cells while the remaining six strains produced ura5 cells. None of the 12 strains produced both ura3 cells and ura5 cells. All 12 isolates of var. neoformans, however, produced ura5 cells and one of them produced ura3 as well as ura5 cells. A genetic lesion in the URA5 gene of an isolate of C. neoformans var. gattii was confirmed by complement with the cognate URA5 gene of C. neoformans var. neoformans. The ura3 isolates were tentatively identified by their ability to grow on a medium containing uridine but not on a medium with orotic acid or orotidine. Enzymatic assays for orotidine-5'-phosphate decarboxylase activity confirmed the isolates to be ura3 mutants. Hybridization analysis of total DNA, digested with EcoRI or StuI and probed with pURA5g2, revealed the presence of only one copy of URA5 in the strains of either variety, regardless of the prevalence of ura5 mutants. Extensive polymorphism was observed in the restriction patterns of the fragments containing the URA5 locus. The prevalence of spontaneously arising ura3 mutants among the isolates of C. neoformans var. gattii, but not among the isolates of C. neoformans var. neoformans, is one more biological difference that distinguishes the two varieties.

Citing Articles

Uncontrolled transposition following RNAi loss causes hypermutation and antifungal drug resistance in clinical isolates of Cryptococcus neoformans.

Priest S, Yadav V, Roth C, Dahlmann T, Kuck U, Magwene P Nat Microbiol. 2022; 7(8):1239-1251.

PMID: 35918426 PMC: 10840647. DOI: 10.1038/s41564-022-01183-z.


Functional Roles of Homologous Recombination and Non-Homologous End Joining in DNA Damage Response and Microevolution in .

Jung K, Jung J, Park H J Fungi (Basel). 2021; 7(7).

PMID: 34356945 PMC: 8307084. DOI: 10.3390/jof7070566.


A spontaneous mutation in DNA polymerase POL3 during in vitro passaging causes a hypermutator phenotype in Cryptococcus species.

Boyce K, Cao C, Xue C, Idnurm A DNA Repair (Amst). 2019; 86:102751.

PMID: 31838381 PMC: 7542539. DOI: 10.1016/j.dnarep.2019.102751.


Natural mismatch repair mutations mediate phenotypic diversity and drug resistance in .

Billmyre R, Clancey S, Heitman J Elife. 2017; 6.

PMID: 28948913 PMC: 5614558. DOI: 10.7554/eLife.28802.


Mismatch Repair of DNA Replication Errors Contributes to Microevolution in the Pathogenic Fungus .

Boyce K, Wang Y, Verma S, Shakya V, Xue C, Idnurm A mBio. 2017; 8(3).

PMID: 28559486 PMC: 5449657. DOI: 10.1128/mBio.00595-17.