Mutualism and asexual reproduction influence recognition genes in a fungal symbiont

dc.contributor.authorVan der Nest, Magrieta Aletta
dc.contributor.authorSteenkamp, Emma Theodora
dc.contributor.authorWilken, Pieter Markus
dc.contributor.authorStenlid, J.
dc.contributor.authorWingfield, Michael J.
dc.contributor.authorWingfield, Brenda D.
dc.contributor.authorSlippers, Bernard
dc.contributor.emailbernard.slippers@fabi.up.ac.zaen_US
dc.date.accessioned2013-10-02T07:05:08Z
dc.date.available2013-10-02T07:05:08Z
dc.date.issued2013-06
dc.description.abstractMutualism between microbes and insects is common and alignment of the reproductive interests of microbial symbionts with this lifestyle typically involves clonal reproduction and vertical transmission by insect partners. Here the Amylostereum funguseSirex woodwasp mutualism was used to consider whether their prolonged association and predominance of asexuality have affected the mating system of the fungal partner. Nucleotide information for the pheromone receptor gene rab1, as well as the translation elongation factor 1a gene and ribosomal RNA internal transcribed spacer region were utilized. The identification of rab1 alleles in Amylostereum chailletii and Amylostereum areolatum populations revealed that this gene is more polymorphic than the other two regions, although the diversity of all three regions was lower than what has been observed in free-living Agaricomycetes. Our data suggest that suppressed recombination might be implicated in the diversification of rab1, while no evidence of balancing selection was detected. We also detected positive selection at only two codons, suggesting that purifying selection is important for the evolution of rab1. The symbiotic relationship with their insect partners has therefore influenced the diversity of this gene and influenced the manner in which selection drives and maintains this diversity in A. areolatum and A. chailletii.en_US
dc.description.librarianhb2013en_US
dc.description.sponsorshipThe National Research Foundation (NRF), members of the Tree Pathology Cooperative Programme (TPCP) and the THRIP initiative of the Department of Trade and Industry (DTI), South Africa.en_US
dc.description.urihttp://www.elsevier.com/locate/funbioen_US
dc.identifier.citationVan der Nest, MA, Steenkamp, ET, Wilken, PM, Stenlid, J, Wingfield, MJ, Wingfield, BD & Slippers, B 2013, 'Mutualism and asexual reproduction influence recognition genes in a fungal symbiont', Fungal Biology, vol. 117, no.6, pp. 439-450.en_US
dc.identifier.issn1878-6146(print)
dc.identifier.issn1878-6162 (online)
dc.identifier.other10.1016/j.funbio.2013.05.001
dc.identifier.urihttp://hdl.handle.net/2263/31872
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rights© 2013 The British Mycological Society. Published by Elsevier Ltd. All rights reserved. Notice : this is the author’s version of a work that was accepted for publication in Fungal Biology. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Fungal Biology, vol.117, no. 6, pp. 439-450, 2013. doi.: 10.1016/j.funbio.2013.05.001en_US
dc.subjectAmylostereum areolatumen_US
dc.subjectPheromone receptor and evolutionen_US
dc.subjectSirex noctilioen_US
dc.subjectSymbiosisen_US
dc.titleMutualism and asexual reproduction influence recognition genes in a fungal symbionten_US
dc.typePostprint Articleen_US

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