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Methodology for Accurate Detection of Mitochondrial DNA Methylation
Published on: May 20, 2018
Codon usage bias analysis of mitochondrial protein-coding genes in 12 species of Candida
Fen Wang1, Nan Zhang, Chunling Zhao
1School of Basic Medical Science, Southwest Medical University, Luzhou 646000, People's Republic of China.songzhangyong83529@126.com.
Abstract:
The incidence of diseases that are caused by fungal infection is gradually increasing, together with antibiotic abuse and the number of patients with hypoimmunity. The many challenges in clinical anti-fungi treatment include serious adverse effects and drug resistance. The mitochondria of fungi have been found to be closely associated with pathopoiesia and drug resistance. Hence, we investigated patterns in Candida mitochondrial genes codon usage bias to provide new information to guide anti-fungal research. According to the nucleotide composition results, most mitochondrial genes of the analysed Candida tended to use A/T bases rather than G/C bases. The relative synonymous codon usage values demonstrated that UUA, AGU, CCU, GCU, UGA, AGA and GGU were the common preferential codons of mitochondrial genes in 12 Candida species. Codon adaptation index (CAI) analysis indicated that the ATP9 of Candida parapsilosis had the highest value, and the ND6 of C. auris had the lowest value. The CAI clearly correlated with the codon bias index, except in C. maltose and C. viswanathii, and was significantly positively correlated with the average GC content. Together, our results suggested that the codon usage pattern is affected by multiple factors, among which GC content is critical. Nucleotide composition, selection pressure and mutation pressure influence codon bias in Candida mitochondrial genes, with dominant status to mutation pressure. Codon usage bias analyses of Candida mitochondrial genes may provide new insight into its evolution.
Insights
Fungal infections are rising, driving research into new antifungal strategies. This study analyzes codon usage bias in Candida mitochondrial genes, revealing mutation pressure as a key factor influencing gene evolution and potential drug resistance.
Area of Science:
- Microbiology and Molecular Biology
- Genetics and Genomics
- Antifungal Drug Discovery
Background:
- Increasing incidence of fungal infections and challenges in current antifungal treatments, including drug resistance and adverse effects.
- Fungal mitochondria are implicated in pathogenicity and drug resistance, making them a target for novel therapies.
- Understanding gene expression patterns, such as codon usage bias, is crucial for developing effective antifungal strategies.
Purpose of the Study:
- To investigate codon usage bias patterns in mitochondrial genes across 12 species of *Candida*.
- To identify factors influencing codon usage bias in *Candida* mitochondrial genes.
- To provide insights into fungal mitochondrial gene evolution and potential targets for antifungal drug development.
Main Methods:
- Analysis of nucleotide composition and codon usage bias in *Candida* mitochondrial genes.
- Calculation of Relative Synonymous Codon Usage (RSCU) and Codon Adaptation Index (CAI).
- Correlation analysis between codon bias, nucleotide composition (GC content), and other evolutionary pressures.
Main Results:
- *Candida* mitochondrial genes predominantly use A/T bases over G/C bases.
- Specific codons (UUA, AGU, CCU, GCU, UGA, AGA, GGU) were identified as preferentially used.
- CAI values varied, with *ATP9* in *C. parapsilosis* showing the highest and *ND6* in *C. auris* the lowest; CAI correlated with codon bias and GC content.
- Mutation pressure was identified as the dominant factor influencing codon bias, followed by nucleotide composition and selection pressure.
Conclusions:
- Codon usage bias in *Candida* mitochondrial genes is shaped by multiple factors, with GC content and mutation pressure being critical.
- These findings offer novel insights into the evolutionary dynamics of fungal mitochondrial genes.
- Understanding codon usage bias can guide the development of new antifungal therapies targeting mitochondrial functions.
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