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Citation for Study 19566

Citation title: "Ectomycorrhizal ecology is imprinted in the genome of the dominant symbiotic fungus Cenococcum geophilum".

Study name: "Ectomycorrhizal ecology is imprinted in the genome of the dominant symbiotic fungus Cenococcum geophilum".

This study is part of submission 19566 (Status: Published).

Citation

Peter M., Kohler A., Ohm R.A., Kuo A., Kr?tzmann J., Morin E., Arend M., Barry K., Binder M., Choi C., Clum A., Copeland A., Grisel N., Haridas S., Kipfer T., Labutti K., Lindquist E., Lipzen A., Maire R., Meier B., Mihaltcheva S., Molinier V., Murat C., P?ggeler S., Quandt C.A., Sperisen C., Tritt A., Tisserant E., Crous P.W., Henrissat B., Nehls U., Egli S., Spatafora J.W., Grigoriev I.V., & Martin F. 2016. Ectomycorrhizal ecology is imprinted in the genome of the dominant symbiotic fungus Cenococcum geophilum. Nature Communications, .

Authors

• Peter M.
• Kohler A.
• Ohm R.A.
• Kuo A.
• Kr?tzmann J.
• Morin E.
• Arend M.
• Barry K.
• Binder M. 508 793-7625
• Choi C.
• Clum A.
• Copeland A.
• Grisel N.
• Haridas S.
• Kipfer T.
• Labutti K.
• Lindquist E.
• Lipzen A.
• Maire R.
• Meier B.
• Mihaltcheva S.
• Molinier V.
• Murat C.
• P?ggeler S.
• Quandt C.A.
• Sperisen C.
• Tritt A.
• Tisserant E.
• Crous P.W.
• Henrissat B.
• Nehls U.
• Egli S.
• Spatafora J.W.
• Grigoriev I.V.
• Martin F.

Abstract

The most frequently encountered symbiont on tree roots is the ascomycete Cenococcum geophilum, the only mycorrhizal species within Dothideomycetes, a class known for devastating plant pathogens. Here we show that the symbiotic genomic idiosyncrasies of ectomycorrhizal basidiomycetes are also present in C. geophilum with symbiosis-induced, taxon-specific genes of unknown function and reduced numbers of plant cell wall-degrading enzymes. C. geophilum still holds a significant set of genes in categories known to be involved in pathogenesis and shows an increased genome size due to transposable elements proliferation. Transcript profiling indicates that C. geophilum likely plays a role in host tree water relations by increased expression of water channels but also by activating biotic-stress related genes known to prime for an enhanced adaptation to drought. The omnipresence of this symbiont on tree roots and its impact on host plant water metabolism call for further studies on mechanisms of host and environmental adaptation.

Keywords

aquaporin, Dothideomycetes, evolution, interaction, mutualist, mycorrhiza, symbiosis

External links

About this resource

• Canonical resource URI: http://purl.org/phylo/treebase/phylows/study/TB2:S19566
• Other versions: Nexus NeXML
• Show BibTeX reference

  		@ARTICLE{TreeBASE2Ref26098,
  	 author = {Martina  Peter and Annegret  Kohler and Robin A. Ohm and Alan  Kuo and Jennifer  Kr?tzmann and Emmanuelle  Morin and Matthias  Arend and Kerrie  Barry and Manfred  Binder and Cindy  Choi and Alicia  Clum and Alex  Copeland and Nadine  Grisel and Sajeet   Haridas and Tabea  Kipfer and Kurt  LaButti and Erika  Lindquist and Anna   Lipzen and Renaud  Maire and Barbara  Meier and Sirma  Mihaltcheva and Virginie  Molinier and Claude  Murat and Stefanie  P?ggeler and C. Alisha Quandt and Christoph  Sperisen and Andrew   Tritt and Emilie  Tisserant and Pedro W. Crous and Bernard  Henrissat and Uwe  Nehls and Simon  Egli and Joseph W. Spatafora and Igor  V Grigoriev and Francis  Martin},
  	 title = {Ectomycorrhizal ecology is imprinted in the genome of the dominant symbiotic fungus Cenococcum geophilum},
  	 year = {2016},
  	 keywords = {aquaporin, Dothideomycetes, evolution, interaction, mutualist, mycorrhiza, symbiosis },
  	 doi = {},
  	 url = {http://},
  	 pmid = {},
  	 journal = {Nature Communications},
  	 volume = {},
  	 number = {},
  	 pages = {},
  	 abstract = {The most frequently encountered symbiont on tree roots is the ascomycete Cenococcum geophilum, the only mycorrhizal species within Dothideomycetes, a class known for devastating plant pathogens. Here we show that the symbiotic genomic idiosyncrasies of ectomycorrhizal basidiomycetes are also present in C. geophilum with symbiosis-induced, taxon-specific genes of unknown function and reduced numbers of plant cell wall-degrading enzymes. C. geophilum still holds a significant set of genes in categories known to be involved in pathogenesis and shows an increased genome size due to transposable elements proliferation. Transcript profiling indicates that C. geophilum likely plays a role in host tree water relations by increased expression of water channels but also by activating biotic-stress related genes known to prime for an enhanced adaptation to drought. The omnipresence of this symbiont on tree roots and its impact on host plant water metabolism call for further studies on mechanisms of host and environmental adaptation.}
  }
  		

• Show RIS reference

  		TY  - JOUR
  ID  - 26098
  AU  - Peter,Martina 
  AU  - Kohler,Annegret 
  AU  - Ohm,Robin A.
  AU  - Kuo,Alan 
  AU  - Kr?tzmann,Jennifer 
  AU  - Morin,Emmanuelle 
  AU  - Arend,Matthias 
  AU  - Barry,Kerrie 
  AU  - Binder,Manfred 
  AU  - Choi,Cindy 
  AU  - Clum,Alicia 
  AU  - Copeland,Alex 
  AU  - Grisel,Nadine 
  AU  - Haridas,Sajeet  
  AU  - Kipfer,Tabea 
  AU  - LaButti,Kurt 
  AU  - Lindquist,Erika 
  AU  - Lipzen,Anna  
  AU  - Maire,Renaud 
  AU  - Meier,Barbara 
  AU  - Mihaltcheva,Sirma 
  AU  - Molinier,Virginie 
  AU  - Murat,Claude 
  AU  - P?ggeler,Stefanie 
  AU  - Quandt,C. Alisha
  AU  - Sperisen,Christoph 
  AU  - Tritt,Andrew  
  AU  - Tisserant,Emilie 
  AU  - Crous,Pedro W.
  AU  - Henrissat,Bernard 
  AU  - Nehls,Uwe 
  AU  - Egli,Simon 
  AU  - Spatafora,Joseph W.
  AU  - Grigoriev,Igor  V
  AU  - Martin,Francis 
  T1  - Ectomycorrhizal ecology is imprinted in the genome of the dominant symbiotic fungus Cenococcum geophilum
  PY  - 2016
  KW  - aquaporin
  KW  - Dothideomycetes
  KW  - evolution
  KW  - interaction
  KW  - mutualist
  KW  - mycorrhiza
  KW  - symbiosis 
  UR  - http://dx.doi.org/
  N2  - The most frequently encountered symbiont on tree roots is the ascomycete Cenococcum geophilum, the only mycorrhizal species within Dothideomycetes, a class known for devastating plant pathogens. Here we show that the symbiotic genomic idiosyncrasies of ectomycorrhizal basidiomycetes are also present in C. geophilum with symbiosis-induced, taxon-specific genes of unknown function and reduced numbers of plant cell wall-degrading enzymes. C. geophilum still holds a significant set of genes in categories known to be involved in pathogenesis and shows an increased genome size due to transposable elements proliferation. Transcript profiling indicates that C. geophilum likely plays a role in host tree water relations by increased expression of water channels but also by activating biotic-stress related genes known to prime for an enhanced adaptation to drought. The omnipresence of this symbiont on tree roots and its impact on host plant water metabolism call for further studies on mechanisms of host and environmental adaptation.
  L3  - 
  JF  - Nature Communications
  VL  - 
  IS  - 
  ER  -