Abstract

To better understand the potential factors contributing to genome instability and phenotypic diversity, we conducted mutation accumulation (MA) experiments for 120 days for 7 diploid cryptococcal hybrids under fluconazole (10 MA lines each) and non-fluconazole conditions (10 MA lines each). The genomic DNA content, loss of heterozygosity (LOH) rate, growth ability, and fluconazole susceptibility were determined for all 140 evolved cultures. Compared to that of their ancestral clones, the evolved clones showed: (i) genomic DNA content changes ranging from ~22% less to ~27% more, and (ii) reduced, similar, and increased phenotypic values for each tested trait, with most evolved clones displaying increased growth at 40 °C and increased fluconazole resistance. Aside from the ancestral multi-locus genotypes (MLGs) and heterozygosity patterns (MHPs), 77 unique MLGs and 70 unique MPHs were identified among the 140 evolved cultures at day 120. The average LOH rates of the MA lines in the absence and presence of fluconazole were similar at 1.27 × 10−4 and 1.38 × 10−4 LOH events per MA line per mitotic division, respectively. While LOH rates varied among MA lines from different ancestors, there was no apparent correlation between the genetic divergence of the parental haploid genomes within ancestral clones and LOH rates. Together, our results suggest that hybrids between diverse lineages of the human pathogenic Cryptococcus can generate significant genotypic and phenotypic diversities during asexual reproduction.

Highlights

  • A stable genome allows faithful transmission of genetic information from parent to progeny, ensuring genotypic and phenotypic stability within individual organisms or populations

  • We aimed to investigate the genome instability of inter-lineage hybrids of human pathogenic Cryptococcus (HPC), including hybrids between lineages within Cryptococcus gattii species complex (CGSC) and hybrids between Cryptococcus neoformans species complex (CNSC) and CGSC

  • The multi-locus heterozygosity patterns and loss of heterozygosity (LOH) rates were estimated based on multi-locus genotype data

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Summary

Introduction

A stable genome allows faithful transmission of genetic information from parent to progeny, ensuring genotypic and phenotypic stability within individual organisms or populations. Genome instability can be manifested in multiple forms and caused by various factors, such as genome doubling, chromosomal rearrangement, mitotic recombination, gene duplication, gene deletion, gene conversion, and transposition Many of these changes involve double-strand DNA breaks, followed by repair through either the synthesis-dependent strand annealing using homologous sequences or non-homologous end joining [1,2]. Among these changes, gene deletion, gene conversion, and, to a lesser extent, mitotic recombination between homologous chromosomes, are commonly manifested as loss of heterozygosity (LOH) that can be detected using multiple molecular methods.

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