Cargando…

The genome assembly of the fungal pathogen Pyrenochaeta lycopersici from Single-Molecule Real-Time sequencing sheds new light on its biological complexity

The first draft genome sequencing of the non-model fungal pathogen Pyrenochaeta lycopersici showed an expansion of gene families associated with heterokaryon incompatibility and lacking of mating-type genes, providing insights into the genetic basis of this “imperfect” fungus which lost the ability...

Descripción completa

Detalles Bibliográficos
Autores principales: Dal Molin, Alessandra, Minio, Andrea, Griggio, Francesca, Delledonne, Massimo, Infantino, Alessandro, Aragona, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6034849/
https://www.ncbi.nlm.nih.gov/pubmed/29979772
http://dx.doi.org/10.1371/journal.pone.0200217
_version_ 1783337948061630464
author Dal Molin, Alessandra
Minio, Andrea
Griggio, Francesca
Delledonne, Massimo
Infantino, Alessandro
Aragona, Maria
author_facet Dal Molin, Alessandra
Minio, Andrea
Griggio, Francesca
Delledonne, Massimo
Infantino, Alessandro
Aragona, Maria
author_sort Dal Molin, Alessandra
collection PubMed
description The first draft genome sequencing of the non-model fungal pathogen Pyrenochaeta lycopersici showed an expansion of gene families associated with heterokaryon incompatibility and lacking of mating-type genes, providing insights into the genetic basis of this “imperfect” fungus which lost the ability to produce the sexual stage. However, due to the Illumina short-read technology, the draft genome was too fragmented to allow a comprehensive characterization of the genome, especially of the repetitive sequence fraction. In this work, the sequencing of another P. lycopersici isolate using long-read Single Molecule Real-Time sequencing technology was performed with the aim of obtaining a gapless genome. Indeed, a gapless genome assembly of 62.7 Mb was obtained, with a fraction of repetitive sequences representing 30% of the total bases. The gene content of the two P. lycopersici isolates was very similar, and the large difference in genome size (about 8 Mb) might be attributable to the high fraction of repetitive sequences detected for the new sequenced isolate. The role of repetitive elements, including transposable elements, in modulating virulence effectors is well established in fungal plant pathogens. Moreover, transposable elements are of fundamental importance in creating and re-modelling genes, especially in imperfect fungi. Their abundance in P. lycopersici, together with the large expansion of heterokaryon incompatibility genes in both sequenced isolates, suggest the presence of possible mechanisms alternative to gene re-assorting mediated by sexual recombination. A quite large fraction (~9%) of repetitive elements in P. lycopersici, has no homology with known classes, strengthening this hypothesis. The availability of a gapless genome of P. lycopersici allowed the in-depth analysis of its genome content, by annotating functional genes and TEs. This goal will be an important resource for shedding light on the evolution of the reproductive and pathogenic behaviour of this soilborne pathogen and the onset of a possible speciation within this species.
format Online
Article
Text
id pubmed-6034849
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-60348492018-07-19 The genome assembly of the fungal pathogen Pyrenochaeta lycopersici from Single-Molecule Real-Time sequencing sheds new light on its biological complexity Dal Molin, Alessandra Minio, Andrea Griggio, Francesca Delledonne, Massimo Infantino, Alessandro Aragona, Maria PLoS One Research Article The first draft genome sequencing of the non-model fungal pathogen Pyrenochaeta lycopersici showed an expansion of gene families associated with heterokaryon incompatibility and lacking of mating-type genes, providing insights into the genetic basis of this “imperfect” fungus which lost the ability to produce the sexual stage. However, due to the Illumina short-read technology, the draft genome was too fragmented to allow a comprehensive characterization of the genome, especially of the repetitive sequence fraction. In this work, the sequencing of another P. lycopersici isolate using long-read Single Molecule Real-Time sequencing technology was performed with the aim of obtaining a gapless genome. Indeed, a gapless genome assembly of 62.7 Mb was obtained, with a fraction of repetitive sequences representing 30% of the total bases. The gene content of the two P. lycopersici isolates was very similar, and the large difference in genome size (about 8 Mb) might be attributable to the high fraction of repetitive sequences detected for the new sequenced isolate. The role of repetitive elements, including transposable elements, in modulating virulence effectors is well established in fungal plant pathogens. Moreover, transposable elements are of fundamental importance in creating and re-modelling genes, especially in imperfect fungi. Their abundance in P. lycopersici, together with the large expansion of heterokaryon incompatibility genes in both sequenced isolates, suggest the presence of possible mechanisms alternative to gene re-assorting mediated by sexual recombination. A quite large fraction (~9%) of repetitive elements in P. lycopersici, has no homology with known classes, strengthening this hypothesis. The availability of a gapless genome of P. lycopersici allowed the in-depth analysis of its genome content, by annotating functional genes and TEs. This goal will be an important resource for shedding light on the evolution of the reproductive and pathogenic behaviour of this soilborne pathogen and the onset of a possible speciation within this species. Public Library of Science 2018-07-06 /pmc/articles/PMC6034849/ /pubmed/29979772 http://dx.doi.org/10.1371/journal.pone.0200217 Text en © 2018 Dal Molin et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Dal Molin, Alessandra
Minio, Andrea
Griggio, Francesca
Delledonne, Massimo
Infantino, Alessandro
Aragona, Maria
The genome assembly of the fungal pathogen Pyrenochaeta lycopersici from Single-Molecule Real-Time sequencing sheds new light on its biological complexity
title The genome assembly of the fungal pathogen Pyrenochaeta lycopersici from Single-Molecule Real-Time sequencing sheds new light on its biological complexity
title_full The genome assembly of the fungal pathogen Pyrenochaeta lycopersici from Single-Molecule Real-Time sequencing sheds new light on its biological complexity
title_fullStr The genome assembly of the fungal pathogen Pyrenochaeta lycopersici from Single-Molecule Real-Time sequencing sheds new light on its biological complexity
title_full_unstemmed The genome assembly of the fungal pathogen Pyrenochaeta lycopersici from Single-Molecule Real-Time sequencing sheds new light on its biological complexity
title_short The genome assembly of the fungal pathogen Pyrenochaeta lycopersici from Single-Molecule Real-Time sequencing sheds new light on its biological complexity
title_sort genome assembly of the fungal pathogen pyrenochaeta lycopersici from single-molecule real-time sequencing sheds new light on its biological complexity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6034849/
https://www.ncbi.nlm.nih.gov/pubmed/29979772
http://dx.doi.org/10.1371/journal.pone.0200217
work_keys_str_mv AT dalmolinalessandra thegenomeassemblyofthefungalpathogenpyrenochaetalycopersicifromsinglemoleculerealtimesequencingshedsnewlightonitsbiologicalcomplexity
AT minioandrea thegenomeassemblyofthefungalpathogenpyrenochaetalycopersicifromsinglemoleculerealtimesequencingshedsnewlightonitsbiologicalcomplexity
AT griggiofrancesca thegenomeassemblyofthefungalpathogenpyrenochaetalycopersicifromsinglemoleculerealtimesequencingshedsnewlightonitsbiologicalcomplexity
AT delledonnemassimo thegenomeassemblyofthefungalpathogenpyrenochaetalycopersicifromsinglemoleculerealtimesequencingshedsnewlightonitsbiologicalcomplexity
AT infantinoalessandro thegenomeassemblyofthefungalpathogenpyrenochaetalycopersicifromsinglemoleculerealtimesequencingshedsnewlightonitsbiologicalcomplexity
AT aragonamaria thegenomeassemblyofthefungalpathogenpyrenochaetalycopersicifromsinglemoleculerealtimesequencingshedsnewlightonitsbiologicalcomplexity
AT dalmolinalessandra genomeassemblyofthefungalpathogenpyrenochaetalycopersicifromsinglemoleculerealtimesequencingshedsnewlightonitsbiologicalcomplexity
AT minioandrea genomeassemblyofthefungalpathogenpyrenochaetalycopersicifromsinglemoleculerealtimesequencingshedsnewlightonitsbiologicalcomplexity
AT griggiofrancesca genomeassemblyofthefungalpathogenpyrenochaetalycopersicifromsinglemoleculerealtimesequencingshedsnewlightonitsbiologicalcomplexity
AT delledonnemassimo genomeassemblyofthefungalpathogenpyrenochaetalycopersicifromsinglemoleculerealtimesequencingshedsnewlightonitsbiologicalcomplexity
AT infantinoalessandro genomeassemblyofthefungalpathogenpyrenochaetalycopersicifromsinglemoleculerealtimesequencingshedsnewlightonitsbiologicalcomplexity
AT aragonamaria genomeassemblyofthefungalpathogenpyrenochaetalycopersicifromsinglemoleculerealtimesequencingshedsnewlightonitsbiologicalcomplexity