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Horizontal Gene Transfer and Gene Dosage Drives Adaptation to Wood Colonization in a Tree Pathogen
PNAS
  • Braham Dhillon, The University of British Columbia
  • Nicolas Feau, The University of British Columbia
  • Andrea Aerts, US Department of Energy Joint Genome Institute
  • Stéphanie Beauseigle, The University of British Columbia
  • Louis Bernier, Université Laval
  • Alex Copeland, US Department of Energy Joint Genome Institute
  • Adam Foster, Canadian Forest Service
  • Navdeep Gill, The University of British Columbia
  • Bernard Henrissat, Centre National de la Recherche Scientifique
  • Padmini Herath, The University of British Columbia
  • Kurt LaButti, US Department of Energy Joint Genome Institute
  • Anthony Levasseur, Aix-Marseille University
  • Erika Lindquist, US Department of Energy Joint Genome Institute
  • Eline Majoor, Utrecht University
  • Robin Ohm, US Department of Energy Joint Genome Institute
  • Jasmyn Pangilinan, US Department of Energy Joint Genome Institute
  • Amadeus Pribowo, The University of British Columbia
  • John Saddler, The University of British Columbia
  • Monique Sakalidis, The University of British Columbia
  • Ronald P. de Vries, Utrecht University
  • Igor Grigoriev, US Department of Energy Joint Genome Institute
  • Stephen Goodwin, Purdue University
  • Philippe Tanguay, Canadian Forest Service
  • Richard Hamelin, Canadian Forest Service
Document Type
Article
Publication Date
3-2-2015
Keywords
  • Poplar Pathogen,
  • Tree Disease,
  • Fungal Genomics,
  • Septoria Canker
Abstract

Some of the most damaging tree pathogens can attack woody stems, causing lesions (cankers) that may be lethal. To identify the genomic determinants of wood colonization leading to canker formation, we sequenced the genomes of the poplar canker pathogen, Mycosphaerella populorum, and the closely related poplar leaf pathogen, M. populicola. A secondary metabolite cluster unique to M. populorum is fully activated following induction by poplar wood and leaves. In addition, genes encoding hemicellulose-degrading enzymes, peptidases, and metabolite transporters were more abundant and were up-regulated in M. populorum growing on poplar wood-chip medium compared with M. populicola. The secondary gene cluster and several of the carbohydrate degradation genes have the signature of horizontal transfer from ascomycete fungi associated with wood decay and from prokaryotes. Acquisition and maintenance of the gene battery necessary for growth in woody tissues and gene dosage resulting in gene expression reconfiguration appear to be responsible for the adaptation of M. populorum to infect, colonize, and cause mortality on poplar woody stems.

Comments

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Additional Comments
This work was supported by the Genomic Research and Development Initiative of Natural Resources Canada, Genome Canada, and Genome BC Project 2112. The work conducted by the US Department of Energy Joint Genome Institute was supported by the Office of Science of the US Department of Energy under Contract DE-AC02-05CH11231. E.M. was supported by a grant from The Netherlands Organization for Scientific Research and The Netherlands Genomics Initiative 93511035 (to R.P.d.V.).
ORCID ID
http://orcid.org/0000-0003-3746-1866
DOI
https://doi.org/10.1073/pnas.1424293112
Citation Information
Braham Dhillon, Nicolas Feau, Andrea Aerts, Stéphanie Beauseigle, et al.. "Horizontal Gene Transfer and Gene Dosage Drives Adaptation to Wood Colonization in a Tree Pathogen" PNAS Vol. 112 Iss. 11 (2015) p. 3451 - 3456 ISSN: 1091-6490
Available at: http://works.bepress.com/navdeep-gill/6/