Cargando…

Molecular Characterization of Vegetative Incompatibility Genes That Restrict Hypovirus Transmission in the Chestnut Blight Fungus Cryphonectria parasitica

Genetic nonself recognition systems such as vegetative incompatibility operate in many filamentous fungi to regulate hyphal fusion between genetically dissimilar individuals and to restrict the spread of virulence-attenuating mycoviruses that have potential for biological control of pathogenic fungi...

Descripción completa

Detalles Bibliográficos
Autores principales: Choi, Gil H., Dawe, Angus L., Churbanov, Alexander, Smith, Myron L., Milgroom, Michael G., Nuss, Donald L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3249360/
https://www.ncbi.nlm.nih.gov/pubmed/22021387
http://dx.doi.org/10.1534/genetics.111.133983
_version_ 1782220338346590208
author Choi, Gil H.
Dawe, Angus L.
Churbanov, Alexander
Smith, Myron L.
Milgroom, Michael G.
Nuss, Donald L.
author_facet Choi, Gil H.
Dawe, Angus L.
Churbanov, Alexander
Smith, Myron L.
Milgroom, Michael G.
Nuss, Donald L.
author_sort Choi, Gil H.
collection PubMed
description Genetic nonself recognition systems such as vegetative incompatibility operate in many filamentous fungi to regulate hyphal fusion between genetically dissimilar individuals and to restrict the spread of virulence-attenuating mycoviruses that have potential for biological control of pathogenic fungi. We report here the use of a comparative genomics approach to identify seven candidate polymorphic genes associated with four vegetative incompatibility (vic) loci of the chestnut blight fungus Cryphonectria parasitica. Disruption of candidate alleles in one of two strains that were heteroallelic at vic2, vic6, or vic7 resulted in enhanced virus transmission, but did not prevent barrage formation associated with mycelial incompatibility. Detailed characterization of the vic6 locus revealed the involvement of nonallelic interactions between two tightly linked genes in barrage formation, heterokaryon formation, and asymmetric, gene-specific influences on virus transmission. The combined results establish molecular identities of genes associated with four C. parasitica vic loci and provide insights into how these recognition factors interact to trigger incompatibility and restrict virus transmission.
format Online
Article
Text
id pubmed-3249360
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Genetics Society of America
record_format MEDLINE/PubMed
spelling pubmed-32493602012-01-31 Molecular Characterization of Vegetative Incompatibility Genes That Restrict Hypovirus Transmission in the Chestnut Blight Fungus Cryphonectria parasitica Choi, Gil H. Dawe, Angus L. Churbanov, Alexander Smith, Myron L. Milgroom, Michael G. Nuss, Donald L. Genetics Investigations Genetic nonself recognition systems such as vegetative incompatibility operate in many filamentous fungi to regulate hyphal fusion between genetically dissimilar individuals and to restrict the spread of virulence-attenuating mycoviruses that have potential for biological control of pathogenic fungi. We report here the use of a comparative genomics approach to identify seven candidate polymorphic genes associated with four vegetative incompatibility (vic) loci of the chestnut blight fungus Cryphonectria parasitica. Disruption of candidate alleles in one of two strains that were heteroallelic at vic2, vic6, or vic7 resulted in enhanced virus transmission, but did not prevent barrage formation associated with mycelial incompatibility. Detailed characterization of the vic6 locus revealed the involvement of nonallelic interactions between two tightly linked genes in barrage formation, heterokaryon formation, and asymmetric, gene-specific influences on virus transmission. The combined results establish molecular identities of genes associated with four C. parasitica vic loci and provide insights into how these recognition factors interact to trigger incompatibility and restrict virus transmission. Genetics Society of America 2012-01 /pmc/articles/PMC3249360/ /pubmed/22021387 http://dx.doi.org/10.1534/genetics.111.133983 Text en Copyright © 2012 by the Genetics Society of America Available freely online through the author-supported open access option.
spellingShingle Investigations
Choi, Gil H.
Dawe, Angus L.
Churbanov, Alexander
Smith, Myron L.
Milgroom, Michael G.
Nuss, Donald L.
Molecular Characterization of Vegetative Incompatibility Genes That Restrict Hypovirus Transmission in the Chestnut Blight Fungus Cryphonectria parasitica
title Molecular Characterization of Vegetative Incompatibility Genes That Restrict Hypovirus Transmission in the Chestnut Blight Fungus Cryphonectria parasitica
title_full Molecular Characterization of Vegetative Incompatibility Genes That Restrict Hypovirus Transmission in the Chestnut Blight Fungus Cryphonectria parasitica
title_fullStr Molecular Characterization of Vegetative Incompatibility Genes That Restrict Hypovirus Transmission in the Chestnut Blight Fungus Cryphonectria parasitica
title_full_unstemmed Molecular Characterization of Vegetative Incompatibility Genes That Restrict Hypovirus Transmission in the Chestnut Blight Fungus Cryphonectria parasitica
title_short Molecular Characterization of Vegetative Incompatibility Genes That Restrict Hypovirus Transmission in the Chestnut Blight Fungus Cryphonectria parasitica
title_sort molecular characterization of vegetative incompatibility genes that restrict hypovirus transmission in the chestnut blight fungus cryphonectria parasitica
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3249360/
https://www.ncbi.nlm.nih.gov/pubmed/22021387
http://dx.doi.org/10.1534/genetics.111.133983
work_keys_str_mv AT choigilh molecularcharacterizationofvegetativeincompatibilitygenesthatrestricthypovirustransmissioninthechestnutblightfunguscryphonectriaparasitica
AT daweangusl molecularcharacterizationofvegetativeincompatibilitygenesthatrestricthypovirustransmissioninthechestnutblightfunguscryphonectriaparasitica
AT churbanovalexander molecularcharacterizationofvegetativeincompatibilitygenesthatrestricthypovirustransmissioninthechestnutblightfunguscryphonectriaparasitica
AT smithmyronl molecularcharacterizationofvegetativeincompatibilitygenesthatrestricthypovirustransmissioninthechestnutblightfunguscryphonectriaparasitica
AT milgroommichaelg molecularcharacterizationofvegetativeincompatibilitygenesthatrestricthypovirustransmissioninthechestnutblightfunguscryphonectriaparasitica
AT nussdonaldl molecularcharacterizationofvegetativeincompatibilitygenesthatrestricthypovirustransmissioninthechestnutblightfunguscryphonectriaparasitica