scholarly journals Evidence for Mitochondrial Genome Methylation in the Yeast Candida albicans: A Potential Novel Epigenetic Mechanism Affecting Adaptation and Pathogenicity?

2018 ◽  
Vol 9 ◽  
Author(s):  
Thais F. Bartelli ◽  
Danielle C. F. Bruno ◽  
Marcelo R. S. Briones
2017 ◽  
Author(s):  
Thais Fernanda Bartelli ◽  
Danielle do Carmo Ferreira Bruno ◽  
Flavio Lichtenstein ◽  
Marcelo R. S. Briones

ABSTRACTInfection byCandida albicansrequires its adaption to physical constraints in the human body, such as low oxygen tension (hypoxia), increased temperature (37°C) and different carbon sources. Previous studies demonstrated that the genetic variability ofC. albicansisolates is an important adaptive mechanism, although little is known about the dynamics of this genetic diversity, and the influence of these environmental conditions on its mitochondrial genome (mtDNA). To test the synergistic effect of these stress conditions onC. albicansgenome, reference strain SC5314 was subjected to anin vitroevolution scheme under hypoxia and 37°C, with two different carbon sources (glycerol and dextrose) for up to 48 weeks (approximately 4,000 generations). Experimental evolution results showed no sequence or copy number changes in the mtDNA, although sequence variants were detected on its nuclear genome by Multilocus sequence typing (MLST) and whole genome sequencing (WGS). After 12 weeks of experimental evolution, sample GTH12, grown under hypoxia at 37°C in glycerol, showed inferior growth and respiratory rates as compared to other conditions tested. Although WGS of GTH12 revealed no variants in its mtDNA, WGS with sodium bisulfite showed a significant reduction in mtDNA methylation in GTH12 in both non-coding and coding regions. Our results provide the first whole mitochondrial genome methylation map ofC. albicansand show that environmental conditions promote the selective growth of specific variants and affect the methylation patterns of the mtDNA in a strain-specific manner.


1992 ◽  
Vol 5 (2) ◽  
pp. 183-203 ◽  
Author(s):  
D R Soll

Most strains of Candida albicans are capable of switching frequently and reversibly between a number of phenotypes distinguishable by colony morphology. A number of different switching systems have been defined according to the limited set of phenotypes in each switching repertoire, and each strain appears to possess a single system. Switching can affect many aspects of cellular physiology and morphology and appears to be a second level of phenotypic variability superimposed upon the bud-hypha transition. The most dramatic switching system so far identified is the "white-opaque transition." This system dramatizes the extraordinary effects switching can have on the budding cell phenotype, including the synthesis of opaque-specific antigens, the expression of white-specific and opaque-specific genes, and the genesis of unique cell wall structures. Switching has been demonstrated to occur at sites of infection and between episodes of recurrent vaginitis, and it may function to generate variability in commensal and infecting populations for adaptive reasons. Although the molecular mechanisms involved in the switch event are not understood, recent approaches to its elucidation are discussed and an epigenetic mechanism is proposed.


2013 ◽  
Vol 34 (2) ◽  
pp. 93-104 ◽  
Author(s):  
Sonja Hrašovec ◽  
Nina Hauptman ◽  
Damjan Glavač ◽  
Franc Jelenc ◽  
Metka Ravnik-Glavač

The identification of novel genes involved in colorectal cancerogenesis is of high clinical relevance for early diagnosis, applying new therapeutic strategies and monitoring disease recurrence, in order to reduce disease incidence and mortality. Gene silencing through CpG island hypermethylation is a major epigenetic mechanism involved in cancer development. In our study, we aimed to identify and validate novel genes with a tumour specific DNA methylation profile in colorectal cancer. We performed a whole-genome methylation scan and identified several possible candidate genes that are hypermethylated in tumour in comparison to healthy colon mucosa. Using methylation-specific high-resolution melting analysis in a set consisting of 133 colorectal cancer samples, we were able to confirm an altered CpG site inTMEM25in 69.2% (92/133) tumours analysed. Furthermore, the expression ofTMEM25was found to be significantly lower in tumour tissue. An inverse correlation between hypermethylation ofTMEM25andTMEM25down-regulated expression was observed.Our results suggest that epigenetic down-regulation ofTMEM25is cancer-related; we thus suggest thatTMEM25hypermethylation might play a significant role in altering expression of this gene in colorectal cancer.


2021 ◽  
Vol 11 (2) ◽  
Author(s):  
Chapman N Beekman ◽  
Christina A Cuomo ◽  
Richard J Bennett ◽  
Iuliana V Ene

Abstract Several Candida species can undergo a heritable and reversible transition from a ‘white’ state to a mating proficient ‘opaque’ state. This ability relies on highly interconnected transcriptional networks that control cell-type-specific gene expression programs over multiple generations. Candida albicans, the most prominent pathogenic Candida species, provides a well-studied paradigm for the white-opaque transition. In this species, a network of at least eight transcriptional regulators controls the balance between white and opaque states that have distinct morphologies, transcriptional profiles, and physiological properties. Given the reversible nature and the high frequency of white-opaque transitions, it is widely assumed that this switch is governed by epigenetic mechanisms that occur independently of any changes in DNA sequence. However, a direct genomic comparison between white and opaque cells has yet to be performed. Here, we present a whole-genome comparative analysis of C. albicans white and opaque cells. This analysis revealed rare genetic changes between cell states, none of which are linked to white-opaque switching. This result is consistent with epigenetic mechanisms controlling cell state differentiation in C. albicans and provides direct evidence against a role for genetic variation in mediating the switch.


2001 ◽  
Vol 183 (3) ◽  
pp. 865-872 ◽  
Author(s):  
James B. Anderson ◽  
Claire Wickens ◽  
Mustafa Khan ◽  
Leah E. Cowen ◽  
Nancy Federspiel ◽  
...  

ABSTRACT Previous analyses of diploid nuclear genotypes have concluded that recombination has occurred in populations of the yeast Candida albicans. To address the possibilities of clonality and recombination in an effectively haploid genome, we sequenced seven regions of mitochondrial DNA (mtDNA) in 45 strains of C. albicans from human immunodeficiency virus-positive patients in Toronto, Canada, and 3 standard reference isolates of C. albicans, CA, CAI4, and WO-1. Among a total of 2,553 nucleotides in the seven regions, 62 polymorphic nucleotide sites and seven indels defined nine distinct mtDNA haplotypes among the 48 strains. Five of these haplotypes occurred in more than one strain, indicating clonal proliferation of mtDNA. Phylogenetic analysis of mtDNA haplotypes resulted in one most-parsimonious tree. Most of the nucleotide sites undergoing parallel change in this tree were clustered in blocks that corresponded to sequenced regions. Because of the existence of these blocks, the apparent homoplasy can be attributed to infrequent, past genetic exchange and recombination between individuals and cannot be attributed to parallel mutation. Among strains sharing the same mtDNA haplotypes, multilocus nuclear genotypes were more similar than expected from a random comparison of nuclear DNA genotypes, suggesting that clonal proliferation of the mitochondrial genome was accompanied by clonal proliferation of the nuclear genome.


RNA Biology ◽  
2021 ◽  
pp. 1-15
Author(s):  
Karolina Łabędzka-Dmoch ◽  
Adam Kolondra ◽  
Magdalena A. Karpińska ◽  
Sonia Dębek ◽  
Joanna Grochowska ◽  
...  

2021 ◽  
Vol 10 (23) ◽  
Author(s):  
Shipra Garg ◽  
Piyush Ranjan ◽  
John R. Erb-Downward ◽  
Gary B. Huffnagle

We report an improved, nearly closed, high-quality draft genome of the Candida albicans CHN1 strain (ATCC MYA-4779), a human isolate, using Illumina and Nanopore sequencing. Covering six complete and two partial nuclear chromosomes along with a partial mitochondrial genome, this assembly is 14,787,852 bases in size, with 5,935 genes.


1996 ◽  
Vol 26 (4) ◽  
pp. 452-460 ◽  
Author(s):  
J. SAVOLAINEN ◽  
A. RANTALA ◽  
M. NERMES ◽  
L. LEHTONEN ◽  
M. VIANDER

Sign in / Sign up

Export Citation Format

Share Document