Mitochondrial genome of Cordyceps blackwelliae: organization, transcription, and evolutionary insights into Cordyceps

Abstract Cordyceps is a diverse genus of insect pathogenic fungi, with about 180 accepted species, including some well-known ones used as ethnic medicine and/or functional food. Nevertheless, mitogenomes are only available for four members of the genus. The current study reports the mitogenome of Co...

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Main Authors: Yong-Jie Zhang, Xiang-Ping Fan, Jia-Ni Li, Shu Zhang
Format: Article
Language:English
Published: BMC 2023-07-01
Series:IMA Fungus
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Online Access:https://doi.org/10.1186/s43008-023-00118-5
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author Yong-Jie Zhang
Xiang-Ping Fan
Jia-Ni Li
Shu Zhang
author_facet Yong-Jie Zhang
Xiang-Ping Fan
Jia-Ni Li
Shu Zhang
author_sort Yong-Jie Zhang
collection DOAJ
description Abstract Cordyceps is a diverse genus of insect pathogenic fungi, with about 180 accepted species, including some well-known ones used as ethnic medicine and/or functional food. Nevertheless, mitogenomes are only available for four members of the genus. The current study reports the mitogenome of Cordyceps blackwelliae, a newly described entomopathogenic fungus. The 42,257-bp mitogenome of the fungus encoded genes typically found in fungal mitogenomes, and a total of 14 introns inserted into seven genes, including cob (1 intron), cox1 (4), cox3 (3), nad1 (1), nad4 (1), nad5 (1), and rnl (3). RNA-Seq analysis revealed differential expression of mitochondrial genes and supported annotations resulting from in silico analysis. There was clear evidence for polycistronic transcription and alternative splicing of mitochondrial genes. Comparison among mitogenomes of five different Cordyceps species (i.e., C. blackwelliae, C. chanhua, C. militaris, C. pruinosa, and C. tenuipes) revealed a high synteny, with mitogenome size expansion correlating with intron insertions. Different mitochondrial protein-coding genes showed variable degrees of genetic differentiation among these species, but they were all under purifying selection. Mitochondrial phylogeny based on either nucleotide or amino acid sequences confirmed the taxonomic position of C. blackwelliae in Cordycipitaceae, clustering together with C. chanhua. This study promotes our understanding of fungal evolution in Cordyceps.
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spelling doaj-art-b311f3bb0b654005a27c101fad7508442025-02-03T05:30:57ZengBMCIMA Fungus2210-63592023-07-0114111710.1186/s43008-023-00118-5Mitochondrial genome of Cordyceps blackwelliae: organization, transcription, and evolutionary insights into CordycepsYong-Jie Zhang0Xiang-Ping Fan1Jia-Ni Li2Shu Zhang3School of Life Science, Shanxi UniversitySchool of Life Science, Shanxi UniversitySchool of Life Science, Shanxi UniversitySchool of Life Science, Shanxi UniversityAbstract Cordyceps is a diverse genus of insect pathogenic fungi, with about 180 accepted species, including some well-known ones used as ethnic medicine and/or functional food. Nevertheless, mitogenomes are only available for four members of the genus. The current study reports the mitogenome of Cordyceps blackwelliae, a newly described entomopathogenic fungus. The 42,257-bp mitogenome of the fungus encoded genes typically found in fungal mitogenomes, and a total of 14 introns inserted into seven genes, including cob (1 intron), cox1 (4), cox3 (3), nad1 (1), nad4 (1), nad5 (1), and rnl (3). RNA-Seq analysis revealed differential expression of mitochondrial genes and supported annotations resulting from in silico analysis. There was clear evidence for polycistronic transcription and alternative splicing of mitochondrial genes. Comparison among mitogenomes of five different Cordyceps species (i.e., C. blackwelliae, C. chanhua, C. militaris, C. pruinosa, and C. tenuipes) revealed a high synteny, with mitogenome size expansion correlating with intron insertions. Different mitochondrial protein-coding genes showed variable degrees of genetic differentiation among these species, but they were all under purifying selection. Mitochondrial phylogeny based on either nucleotide or amino acid sequences confirmed the taxonomic position of C. blackwelliae in Cordycipitaceae, clustering together with C. chanhua. This study promotes our understanding of fungal evolution in Cordyceps.https://doi.org/10.1186/s43008-023-00118-5Cordyceps blackwelliaeMitogenomeTranscriptomePhylogenyCordycipitaceaeEvolution
spellingShingle Yong-Jie Zhang
Xiang-Ping Fan
Jia-Ni Li
Shu Zhang
Mitochondrial genome of Cordyceps blackwelliae: organization, transcription, and evolutionary insights into Cordyceps
IMA Fungus
Cordyceps blackwelliae
Mitogenome
Transcriptome
Phylogeny
Cordycipitaceae
Evolution
title Mitochondrial genome of Cordyceps blackwelliae: organization, transcription, and evolutionary insights into Cordyceps
title_full Mitochondrial genome of Cordyceps blackwelliae: organization, transcription, and evolutionary insights into Cordyceps
title_fullStr Mitochondrial genome of Cordyceps blackwelliae: organization, transcription, and evolutionary insights into Cordyceps
title_full_unstemmed Mitochondrial genome of Cordyceps blackwelliae: organization, transcription, and evolutionary insights into Cordyceps
title_short Mitochondrial genome of Cordyceps blackwelliae: organization, transcription, and evolutionary insights into Cordyceps
title_sort mitochondrial genome of cordyceps blackwelliae organization transcription and evolutionary insights into cordyceps
topic Cordyceps blackwelliae
Mitogenome
Transcriptome
Phylogeny
Cordycipitaceae
Evolution
url https://doi.org/10.1186/s43008-023-00118-5
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