Diversity of MSDIN family members in amanitin-producing mushrooms and the phylogeny of the MSDIN and prolyl oligopeptidase genes.


Journal

BMC genomics
ISSN: 1471-2164
Titre abrégé: BMC Genomics
Pays: England
ID NLM: 100965258

Informations de publication

Date de publication:
26 Jun 2020
Historique:
received: 23 01 2020
accepted: 22 06 2020
entrez: 28 6 2020
pubmed: 28 6 2020
medline: 2 2 2021
Statut: epublish

Résumé

Amanitin-producing mushrooms, mainly distributed in the genera Amanita, Galerina and Lepiota, possess MSDIN gene family for the biosynthesis of many cyclopeptides catalysed by prolyl oligopeptidase (POP). Recently, transcriptome sequencing has proven to be an efficient way to mine MSDIN and POP genes in these lethal mushrooms. Thus far, only A. palloides and A. bisporigera from North America and A. exitialis and A. rimosa from Asia have been studied based on transcriptome analysis. However, the MSDIN and POP genes of many amanitin-producing mushrooms in China remain unstudied; hence, the transcriptomes of these speices deserve to be analysed. In this study, the MSDIN and POP genes from ten Amanita species, two Galerina species and Lepiota venenata were studied and the phylogenetic relationships of their MSDIN and POP genes were analysed. Through transcriptome sequencing and PCR cloning, 19 POP genes and 151 MSDIN genes predicted to encode 98 non-duplicated cyclopeptides, including α-amanitin, β-amanitin, phallacidin, phalloidin and 94 unknown peptides, were found in these species. Phylogenetic analysis showed that (1) MSDIN genes generally clustered depending on the taxonomy of the genus, while Amanita MSDIN genes clustered depending on the chemical substance; and (2) the POPA genes of Amanita, Galerina and Lepiota clustered and were separated into three different groups, but the POPB genes of the three distinct genera were clustered in a highly supported monophyletic group. These results indicate that lethal Amanita species have the genetic capacity to produce numerous cyclopeptides, most of which are unknown, while lethal Galerina and Lepiota species seem to only have the genetic capacity to produce α-amanitin. Additionally, the POPB phylogeny of Amanita, Galerina and Lepiota conflicts with the taxonomic status of the three genera, suggesting that underlying horizontal gene transfer has occurred among these three genera.

Sections du résumé

BACKGROUND BACKGROUND
Amanitin-producing mushrooms, mainly distributed in the genera Amanita, Galerina and Lepiota, possess MSDIN gene family for the biosynthesis of many cyclopeptides catalysed by prolyl oligopeptidase (POP). Recently, transcriptome sequencing has proven to be an efficient way to mine MSDIN and POP genes in these lethal mushrooms. Thus far, only A. palloides and A. bisporigera from North America and A. exitialis and A. rimosa from Asia have been studied based on transcriptome analysis. However, the MSDIN and POP genes of many amanitin-producing mushrooms in China remain unstudied; hence, the transcriptomes of these speices deserve to be analysed.
RESULTS RESULTS
In this study, the MSDIN and POP genes from ten Amanita species, two Galerina species and Lepiota venenata were studied and the phylogenetic relationships of their MSDIN and POP genes were analysed. Through transcriptome sequencing and PCR cloning, 19 POP genes and 151 MSDIN genes predicted to encode 98 non-duplicated cyclopeptides, including α-amanitin, β-amanitin, phallacidin, phalloidin and 94 unknown peptides, were found in these species. Phylogenetic analysis showed that (1) MSDIN genes generally clustered depending on the taxonomy of the genus, while Amanita MSDIN genes clustered depending on the chemical substance; and (2) the POPA genes of Amanita, Galerina and Lepiota clustered and were separated into three different groups, but the POPB genes of the three distinct genera were clustered in a highly supported monophyletic group.
CONCLUSIONS CONCLUSIONS
These results indicate that lethal Amanita species have the genetic capacity to produce numerous cyclopeptides, most of which are unknown, while lethal Galerina and Lepiota species seem to only have the genetic capacity to produce α-amanitin. Additionally, the POPB phylogeny of Amanita, Galerina and Lepiota conflicts with the taxonomic status of the three genera, suggesting that underlying horizontal gene transfer has occurred among these three genera.

Identifiants

pubmed: 32590929
doi: 10.1186/s12864-020-06857-8
pii: 10.1186/s12864-020-06857-8
pmc: PMC7318481
doi:

Substances chimiques

Amanitins 0
Fungal Proteins 0
Peptides, Cyclic 0
Prolyl Oligopeptidases EC 3.4.21.26

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

440

Subventions

Organisme : National Natural Science Foundation of China
ID : Grant No. 31872616
Organisme : Scientific Research Foundation of Hunan Provincial Education Department
ID : Grant no. 18A026

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Auteurs

Zhengmi He (Z)

College of Life Science, Hunan Normal University, Lushan Road, Changsha, 410081, China.

Pan Long (P)

College of Life Science, Hunan Normal University, Lushan Road, Changsha, 410081, China.

Fang Fang (F)

College of Life Science, Hunan Normal University, Lushan Road, Changsha, 410081, China.

Sainan Li (S)

College of Life Science, Hunan Normal University, Lushan Road, Changsha, 410081, China.

Ping Zhang (P)

College of Life Science, Hunan Normal University, Lushan Road, Changsha, 410081, China.

Zuohong Chen (Z)

College of Life Science, Hunan Normal University, Lushan Road, Changsha, 410081, China. chenzuohong@263.net.

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Classifications MeSH