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Autori principali: Tan, Suxu, Wang, Wenwen, Li, Jinjiang, Sha, Zhenxia
Natura: Artículo científico
Lingua:en
Pubblicazione: BMC genomics 2025
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Accesso online:https://pubmed.ncbi.nlm.nih.gov/39833664/
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author Tan, Suxu
Wang, Wenwen
Li, Jinjiang
Sha, Zhenxia
author_facet Tan, Suxu
Wang, Wenwen
Li, Jinjiang
Sha, Zhenxia
Tan, Suxu
Wang, Wenwen
Li, Jinjiang
Sha, Zhenxia
collection PubMed - marine biology
contents Comprehensive analysis of 111 Pleuronectiformes mitochondrial genomes: insights into structure, conservation, variation and evolution. Tan, Suxu Wang, Wenwen Li, Jinjiang Sha, Zhenxia Animals Genome, Mitochondrial Flatfishes Phylogeny Evolution, Molecular Genetic Variation Codon Usage Genomics RNA, Transfer Conserved Sequence Pleuronectiformes, also known as flatfish, are important model and economic animals. However, a comprehensive genome survey of their important organelles, mitochondria, has been limited. Therefore, we aim to analyze the genomic structure, codon preference, nucleotide diversity, selective pressure and repeat sequences, as well as reconstruct the phylogenetic relationship using the mitochondrial genomes of 111 flatfish species. Our analysis revealed a conserved gene content of protein-coding genes and rRNA genes, but varying numbers of tRNA genes and control regions across species. Various gene rearrangements were found in flatfish species, especially for the rearrangement of nad5-nad6-cytb block in Samaridae family, the swapping rearrangement of nad6 and cytb gene in Bothidae family, as well as the control region translocation and tRNA-Gln gene inversion in the subfamily Cynoglossinae, suggesting their unique evolutionary history and/or functional benefit. Codon usage showed obvious biases, with adenine being the most frequent nucleotide at the third codon position. Nucleotide diversity and selective pressure analysis suggested that different protein-coding genes underwent varying degrees of evolutionary pressure, with cytb and cox genes being the most conserved ones. Phylogenetic analysis using both whole mitogenome information and concatenated independently aligned protein-coding genes largely mirrored the taxonomic classification of the species, but showed different phylogeny. The identification of simple sequence repeats and various long repetitive sequences provided additional complexity of genome organization and offered markers for evolutionary studies and breeding practices. This study represents a significant step forward in our comprehension of the flatfish mitochondrial genomes, providing valuable insights into the structure, conservation and variation within flatfish mitogenomes, with implications for understanding their evolutionary history, functional genomics and fisheries management. Future research can delve deeper into conservation biology, evolutionary biology and functional usages of variations.
format Artículo científico
id pubmed_39833664
institution PubMed
language en
publishDate 2025
publisher BMC genomics
record_format pubmed
spellingShingle Comprehensive analysis of 111 Pleuronectiformes mitochondrial genomes: insights into structure, conservation, variation and evolution.
Tan, Suxu
Wang, Wenwen
Li, Jinjiang
Sha, Zhenxia
Animals
Genome, Mitochondrial
Flatfishes
Phylogeny
Evolution, Molecular
Genetic Variation
Codon Usage
Genomics
RNA, Transfer
Conserved Sequence
Comprehensive analysis of 111 Pleuronectiformes mitochondrial genomes: insights into structure, conservation, variation and evolution. Tan, Suxu Wang, Wenwen Li, Jinjiang Sha, Zhenxia Animals Genome, Mitochondrial Flatfishes Phylogeny Evolution, Molecular Genetic Variation Codon Usage Genomics RNA, Transfer Conserved Sequence Pleuronectiformes, also known as flatfish, are important model and economic animals. However, a comprehensive genome survey of their important organelles, mitochondria, has been limited. Therefore, we aim to analyze the genomic structure, codon preference, nucleotide diversity, selective pressure and repeat sequences, as well as reconstruct the phylogenetic relationship using the mitochondrial genomes of 111 flatfish species. Our analysis revealed a conserved gene content of protein-coding genes and rRNA genes, but varying numbers of tRNA genes and control regions across species. Various gene rearrangements were found in flatfish species, especially for the rearrangement of nad5-nad6-cytb block in Samaridae family, the swapping rearrangement of nad6 and cytb gene in Bothidae family, as well as the control region translocation and tRNA-Gln gene inversion in the subfamily Cynoglossinae, suggesting their unique evolutionary history and/or functional benefit. Codon usage showed obvious biases, with adenine being the most frequent nucleotide at the third codon position. Nucleotide diversity and selective pressure analysis suggested that different protein-coding genes underwent varying degrees of evolutionary pressure, with cytb and cox genes being the most conserved ones. Phylogenetic analysis using both whole mitogenome information and concatenated independently aligned protein-coding genes largely mirrored the taxonomic classification of the species, but showed different phylogeny. The identification of simple sequence repeats and various long repetitive sequences provided additional complexity of genome organization and offered markers for evolutionary studies and breeding practices. This study represents a significant step forward in our comprehension of the flatfish mitochondrial genomes, providing valuable insights into the structure, conservation and variation within flatfish mitogenomes, with implications for understanding their evolutionary history, functional genomics and fisheries management. Future research can delve deeper into conservation biology, evolutionary biology and functional usages of variations.
title Comprehensive analysis of 111 Pleuronectiformes mitochondrial genomes: insights into structure, conservation, variation and evolution.
topic Animals
Genome, Mitochondrial
Flatfishes
Phylogeny
Evolution, Molecular
Genetic Variation
Codon Usage
Genomics
RNA, Transfer
Conserved Sequence
url https://pubmed.ncbi.nlm.nih.gov/39833664/