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Hession, C.

Publications and source records attributed to Hession, C..

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Centromeres in budding yeasts are conserved in chromosomal location but not in structure.

The budding yeast Saccharomyces cerevisiae has point centromeres, which are much smaller and simpler than centromeres of most other eukaryotes and have a defined DNA sequence. Other yeast taxa have different and highly diverse centromere structures, but a clear picture of how yeast centromeres have evolved is lacking. Here, we investigated nine yeast species in two taxonomic orders that are close outgroups to S. cerevisiae. We find that they have a wide diversity of centromere structures, indicating that multiple transitions of structure have occurred within the last 200 Myr. Some species have centromeres with defined sequence motifs (17 - 200 bp), others consist of Inverted Repeats (IRs), and others have Ty5-like retroelement clusters. Strikingly, the chromosomal locations of centromeres have largely been conserved across taxonomic orders, even as their structures have changed, which suggests that structure replacement occurs in situ. In some Barnettozyma species we find that a single genome can contain chromosomes with different centromere structures - some with IRs and some without - which suggests that a structural transition is underway in this genus. We identified only one example of a centromere moving by a long distance: a new centromere formed recently at the MAT locus of Barnettozyma californica, 250 kb from the previous centromere on that chromosome. Author summaryCentromeres are an evolutionary paradox. Their molecular function is highly conserved, but their structures vary tremendously among eukaryotes. The "point" centromeres of the yeast Saccharomyces cerevisiae are among the most unusual: they are tiny (< 200 bp) and non-repetitive, and unlike other centromeres they contain a single copy of a well-defined sequence motif. However, we have little knowledge about where these point centromeres came from, or more generally about how changes of centromere structure occur during evolution. Here, we characterized centromere structure and location in nine species of budding yeasts, spanning an evolutionary depth of approximately 200 million years. We find that the chromosomal locations of centromeres are extraordinarily well conserved, whereas their structures vary greatly. We show that sequence-defined centromeres are older and more widely distributed than previously realised. We identify some species in which the centromeres of different chromosomes have different structures, which suggests that they are in transition from one structure to another. The centromere variation observed makes it difficult to infer the ancestral structure.

evolutionary biology↗

Small pangenome of Candida parapsilosis reflects overall low intraspecific diversity

Candida parapsilosis is an opportunistic yeast pathogen that can cause life-threatening infections in immunocompromised humans. Whole genome sequencing (WGS) studies of the species have demonstrated remarkably low diversity, with strains typically differing by about 1.5 single nucleotide polymorphisms (SNPs) per 10 kb. However, SNP calling alone does not capture the full extent of genetic variation. Here, we define the pangenome of 372 C. parapsilosis isolates to determine variation in gene content. The pangenome consists of 5,859 genes, of which 48 are not found in the genome of the reference strain. This includes 5,791 core genes (present in [&ge;] 99.5% of isolates). Four genes, including the allantoin permease gene DAL4, were present in all isolates but were truncated in some strains. The truncated DAL4 was classified as a pseudogene in the reference strain CDC317. CRISPR-Cas9 gene editing showed that removing the early stop codon (producing the full-length Dal4 protein) is associated with improved use of allantoin as a sole nitrogen source. We find that the accessory genome of C. parapsilosis consists of 68 homologous clusters. This includes 38 previously annotated genes, 27 novel paralogs of previously annotated genes and 3 uncharacterised ORFs. Approximately one-third of the accessory genome (24/68 genes) is associated with gene fusions between tandem genes in the major facilitator superfamily (MFS). Additionally, we identified two highly divergent C. parapsilosis strains and find that, despite their increased phylogenetic distance ([~]30 SNPs per 10 kb), both strains have similar gene content to the other 372. ImportanceCandida parapsilosis is a human fungal pathogen, listed in the high priority group by the World Health Organisation. It is an increasing cause of hospital-acquired and drug-resistant infection. Here, we studied the genetic diversity of 372 C. parapsilosis isolates, the largest genomic surveillance of this species to date. We show that there is relatively little genetic variation. However, we identified two more distantly-related isolates from Germany, suggesting that even more sampling may yield more diversity. We find that the pangenome (the cumulative gene content of all isolates) is surprisingly small, compared to other fungal species. Many of the non-core genes are involved in transport. We also find that variations in gene content are associated with nitrogen metabolism, which may contribute to the virulence characteristics of this species.

genomics↗