Genome‐wide alternative splicing profiling in the fungal plant pathogen Sclerotinia sclerotiorum during the colonization of diverse host families

Sclerotinia sclerotiorum is a notorious generalist plant pathogen that threatens more than 600 host plants, including wild and cultivated species. The molecular bases underlying the broad compatibility of S. sclerotiorum with its hosts is not fully elucidated. In contrast to higher plants and animal...

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Published inMolecular plant pathology Vol. 22; no. 1; pp. 31 - 47
Main Authors Ibrahim, Heba M.M., Kusch, Stefan, Didelon, Marie, Raffaele, Sylvain
Format Journal Article
LanguageEnglish
Published England John Wiley & Sons, Inc 01.01.2021
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Abstract Sclerotinia sclerotiorum is a notorious generalist plant pathogen that threatens more than 600 host plants, including wild and cultivated species. The molecular bases underlying the broad compatibility of S. sclerotiorum with its hosts is not fully elucidated. In contrast to higher plants and animals, alternative splicing (AS) is not well studied in plant‐pathogenic fungi. AS is a common regulated cellular process that increases cell protein and RNA diversity. In this study, we annotated spliceosome genes in the genome of S. sclerotiorum and characterized their expression in vitro and during the colonization of six host species. Several spliceosome genes were differentially expressed in planta, suggesting that AS was altered during infection. Using stringent parameters, we identified 1,487 S. sclerotiorum genes differentially expressed in planta and exhibiting alternative transcripts. The most common AS events during the colonization of all plants were retained introns and the alternative 3′ receiver site. We identified S. sclerotiorum genes expressed in planta for which (a) the relative accumulation of alternative transcripts varies according to the host being colonized and (b) alternative transcripts harbour distinct protein domains. This notably included 42 genes encoding predicted secreted proteins showing high‐confidence AS events. This study indicates that AS events are taking place in the plant pathogenic fungus S. sclerotiorum during the colonization of host plants and could generate functional diversity in the repertoire of proteins secreted by S. sclerotiorum during infection. Alternative splicing occurs in the plant‐pathogenic fungus Sclerotinia sclerotiorum during colonization of diverse host plants and could generate functional diversity in the repertoire of secreted proteins.
AbstractList Abstract Sclerotinia sclerotiorum is a notorious generalist plant pathogen that threatens more than 600 host plants, including wild and cultivated species. The molecular bases underlying the broad compatibility of S. sclerotiorum with its hosts is not fully elucidated. In contrast to higher plants and animals, alternative splicing (AS) is not well studied in plant‐pathogenic fungi. AS is a common regulated cellular process that increases cell protein and RNA diversity. In this study, we annotated spliceosome genes in the genome of S. sclerotiorum and characterized their expression in vitro and during the colonization of six host species. Several spliceosome genes were differentially expressed in planta, suggesting that AS was altered during infection. Using stringent parameters, we identified 1,487 S. sclerotiorum genes differentially expressed in planta and exhibiting alternative transcripts. The most common AS events during the colonization of all plants were retained introns and the alternative 3′ receiver site. We identified S. sclerotiorum genes expressed in planta for which (a) the relative accumulation of alternative transcripts varies according to the host being colonized and (b) alternative transcripts harbour distinct protein domains. This notably included 42 genes encoding predicted secreted proteins showing high‐confidence AS events. This study indicates that AS events are taking place in the plant pathogenic fungus S. sclerotiorum during the colonization of host plants and could generate functional diversity in the repertoire of proteins secreted by S. sclerotiorum during infection.
Sclerotinia sclerotiorum is a notorious generalist plant pathogen that threatens more than 600 host plants, including wild and cultivated species. The molecular bases underlying the broad compatibility of S. sclerotiorum with its hosts is not fully elucidated. In contrast to higher plants and animals, alternative splicing (AS) is not well studied in plant‐pathogenic fungi. AS is a common regulated cellular process that increases cell protein and RNA diversity. In this study, we annotated spliceosome genes in the genome of S. sclerotiorum and characterized their expression in vitro and during the colonization of six host species. Several spliceosome genes were differentially expressed in planta, suggesting that AS was altered during infection. Using stringent parameters, we identified 1,487 S. sclerotiorum genes differentially expressed in planta and exhibiting alternative transcripts. The most common AS events during the colonization of all plants were retained introns and the alternative 3′ receiver site. We identified S. sclerotiorum genes expressed in planta for which (a) the relative accumulation of alternative transcripts varies according to the host being colonized and (b) alternative transcripts harbour distinct protein domains. This notably included 42 genes encoding predicted secreted proteins showing high‐confidence AS events. This study indicates that AS events are taking place in the plant pathogenic fungus S. sclerotiorum during the colonization of host plants and could generate functional diversity in the repertoire of proteins secreted by S. sclerotiorum during infection.
Mol Plant Pathol. 2020;00:1-17. | 1 wileyonlinelibrary.com/journal/mpp 1 | INTRODUC TI ON Sclerotinia sclerotiorum is a plant-parasitic fungus that causes white mould disease. It is known for its aggressive necrotrophic lifestyle, which means that the fungus actively kills the plant host cells and thrives by feeding on the dead plant material, and for exhibiting a broad host range. S. sclerotiorum can infect more than 600 host plants including economically important species such as tomato Abstract Sclerotinia sclerotiorum is a notorious generalist plant pathogen that threatens more than 600 host plants, including wild and cultivated species. The molecular bases underlying the broad compatibility of S. sclerotiorum with its hosts is not fully elucidated. In contrast to higher plants and animals, alternative splicing (AS) is not well studied in plant-pathogenic fungi. AS is a common regulated cellular process that increases cell protein and RNA diversity. In this study, we annotated spliceosome genes in the genome of S. sclerotiorum and characterized their expression in vitro and during the colonization of six host species. Several spliceosome genes were differentially expressed in planta, suggesting that AS was altered during infection. Using stringent parameters, we identified 1,487 S. sclerotiorum genes differentially expressed in planta and exhibiting alternative transcripts. The most common AS events during the colonization of all plants were retained introns and the alternative 3′ receiver site. We identified S. sclerotiorum genes expressed in planta for which (a) the relative accumulation of alternative transcripts varies according to the host being colonized and (b) alternative transcripts harbour distinct protein domains. This notably included 42 genes encoding predicted secreted proteins showing high-confidence AS events. This study indicates that AS events are taking place in the plant pathogenic fungus S. sclerotiorum during the colonization of host plants and could generate functional diversity in the repertoire of proteins secreted by S. sclerotiorum during infection. K E Y W O R D S alternative splicing, computational analysis, host adaptation, isoforms, RNA sequencing (RNA-seq), Sclerotinia sclerotiorum
Sclerotinia sclerotiorum is a notorious generalist plant pathogen that threatens more than 600 host plants, including wild and cultivated species. The molecular bases underlying the broad compatibility of S. sclerotiorum with its hosts is not fully elucidated. In contrast to higher plants and animals, alternative splicing (AS) is not well studied in plant‐pathogenic fungi. AS is a common regulated cellular process that increases cell protein and RNA diversity. In this study, we annotated spliceosome genes in the genome of S. sclerotiorum and characterized their expression in vitro and during the colonization of six host species. Several spliceosome genes were differentially expressed in planta, suggesting that AS was altered during infection. Using stringent parameters, we identified 1,487 S. sclerotiorum genes differentially expressed in planta and exhibiting alternative transcripts. The most common AS events during the colonization of all plants were retained introns and the alternative 3′ receiver site. We identified S. sclerotiorum genes expressed in planta for which (a) the relative accumulation of alternative transcripts varies according to the host being colonized and (b) alternative transcripts harbour distinct protein domains. This notably included 42 genes encoding predicted secreted proteins showing high‐confidence AS events. This study indicates that AS events are taking place in the plant pathogenic fungus S. sclerotiorum during the colonization of host plants and could generate functional diversity in the repertoire of proteins secreted by S. sclerotiorum during infection. Alternative splicing occurs in the plant‐pathogenic fungus Sclerotinia sclerotiorum during colonization of diverse host plants and could generate functional diversity in the repertoire of secreted proteins.
Sclerotinia sclerotiorum is a notorious generalist plant pathogen that threatens more than 600 host plants, including wild and cultivated species. The molecular bases underlying the broad compatibility of S. sclerotiorum with its hosts is not fully elucidated. In contrast to higher plants and animals, alternative splicing (AS) is not well studied in plant‐pathogenic fungi. AS is a common regulated cellular process that increases cell protein and RNA diversity. In this study, we annotated spliceosome genes in the genome of S. sclerotiorum and characterized their expression in vitro and during the colonization of six host species. Several spliceosome genes were differentially expressed in planta, suggesting that AS was altered during infection. Using stringent parameters, we identified 1,487 S. sclerotiorum genes differentially expressed in planta and exhibiting alternative transcripts. The most common AS events during the colonization of all plants were retained introns and the alternative 3′ receiver site. We identified S. sclerotiorum genes expressed in planta for which (a) the relative accumulation of alternative transcripts varies according to the host being colonized and (b) alternative transcripts harbour distinct protein domains. This notably included 42 genes encoding predicted secreted proteins showing high‐confidence AS events. This study indicates that AS events are taking place in the plant pathogenic fungus S. sclerotiorum during the colonization of host plants and could generate functional diversity in the repertoire of proteins secreted by S. sclerotiorum during infection. Alternative splicing occurs in the plant‐pathogenic fungus Sclerotinia sclerotiorum during colonization of diverse host plants and could generate functional diversity in the repertoire of secreted proteins.
Sclerotinia sclerotiorum is a notorious generalist plant pathogen that threatens more than 600 host plants, including wild and cultivated species. The molecular bases underlying the broad compatibility of S. sclerotiorum with its hosts is not fully elucidated. In contrast to higher plants and animals, alternative splicing (AS) is not well studied in plant-pathogenic fungi. AS is a common regulated cellular process that increases cell protein and RNA diversity. In this study, we annotated spliceosome genes in the genome of S. sclerotiorum and characterized their expression in vitro and during the colonization of six host species. Several spliceosome genes were differentially expressed in planta, suggesting that AS was altered during infection. Using stringent parameters, we identified 1,487 S. sclerotiorum genes differentially expressed in planta and exhibiting alternative transcripts. The most common AS events during the colonization of all plants were retained introns and the alternative 3' receiver site. We identified S. sclerotiorum genes expressed in planta for which (a) the relative accumulation of alternative transcripts varies according to the host being colonized and (b) alternative transcripts harbour distinct protein domains. This notably included 42 genes encoding predicted secreted proteins showing high-confidence AS events. This study indicates that AS events are taking place in the plant pathogenic fungus S. sclerotiorum during the colonization of host plants and could generate functional diversity in the repertoire of proteins secreted by S. sclerotiorum during infection.
Audience Academic
Author Kusch, Stefan
Ibrahim, Heba M.M.
Raffaele, Sylvain
Didelon, Marie
AuthorAffiliation 3 Present address: Plant Health and Protection Division of Plant Biotechnics Department of Biosystems Faculty of Bioscience Engineering KU Leuven Leuven Belgium
1 LIPM, Université de Toulouse INRAE CNRS Castanet‐Tolosan France
2 Genetics Department Faculty of Agriculture Cairo University Giza Egypt
4 Present address: Unit of Plant Molecular Cell Biology Institute for Biology I RWTH Aachen University Aachen Germany
AuthorAffiliation_xml – name: 1 LIPM, Université de Toulouse INRAE CNRS Castanet‐Tolosan France
– name: 2 Genetics Department Faculty of Agriculture Cairo University Giza Egypt
– name: 4 Present address: Unit of Plant Molecular Cell Biology Institute for Biology I RWTH Aachen University Aachen Germany
– name: 3 Present address: Plant Health and Protection Division of Plant Biotechnics Department of Biosystems Faculty of Bioscience Engineering KU Leuven Leuven Belgium
Author_xml – sequence: 1
  givenname: Heba M.M.
  orcidid: 0000-0003-0603-7755
  surname: Ibrahim
  fullname: Ibrahim, Heba M.M.
  email: heba.ibrahim@kuleuven.be
  organization: Cairo University
– sequence: 2
  givenname: Stefan
  orcidid: 0000-0002-2472-5255
  surname: Kusch
  fullname: Kusch, Stefan
  organization: CNRS
– sequence: 3
  givenname: Marie
  orcidid: 0000-0002-8458-8117
  surname: Didelon
  fullname: Didelon, Marie
  organization: CNRS
– sequence: 4
  givenname: Sylvain
  orcidid: 0000-0002-2442-9632
  surname: Raffaele
  fullname: Raffaele, Sylvain
  email: sylvain.raffaele@inrae.fr
  organization: CNRS
BackLink https://www.ncbi.nlm.nih.gov/pubmed/33111422$$D View this record in MEDLINE/PubMed
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Issue 1
Keywords RNA sequencing (RNA-seq)
Sclerotinia sclerotiorum
isoforms
host adaptation
computational analysis
alternative splicing
Language English
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PublicationTitle Molecular plant pathology
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Snippet Sclerotinia sclerotiorum is a notorious generalist plant pathogen that threatens more than 600 host plants, including wild and cultivated species. The...
Abstract Sclerotinia sclerotiorum is a notorious generalist plant pathogen that threatens more than 600 host plants, including wild and cultivated species. The...
Mol Plant Pathol. 2020;00:1-17. | 1 wileyonlinelibrary.com/journal/mpp 1 | INTRODUC TI ON Sclerotinia sclerotiorum is a plant-parasitic fungus that causes...
Sclerotinia sclerotiorum is a notorious generalist plant pathogen that threatens more than 600 host plants, including wild and cultivated species. The...
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SubjectTerms Alternative splicing
Colonization
computational analysis
Fungi
Gene expression
Genes
Genetic research
Genomes
Genomics
host adaptation
Host plants
Infections
Introns
isoforms
Kinases
Life Sciences
Original
Parameter identification
Pathogens
Proteins
Ribonucleic acid
RNA
RNA sequencing (RNA‐seq)
Sclerotinia sclerotiorum
Signal transduction
Splicing
Virulence
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Title Genome‐wide alternative splicing profiling in the fungal plant pathogen Sclerotinia sclerotiorum during the colonization of diverse host families
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fmpp.13006
https://www.ncbi.nlm.nih.gov/pubmed/33111422
https://www.proquest.com/docview/2471193386
https://hal.inrae.fr/hal-03007953
https://pubmed.ncbi.nlm.nih.gov/PMC7749757
Volume 22
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