Elucidating the genetic landscape of cellular morphogenesis in an obligate fungal symbiont

Research output: Contribution to conferencePosterResearchpeer-review

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Elucidating the genetic landscape of cellular morphogenesis in an obligate fungal symbiont. / de Fine Licht, Henrik Hjarvard; Tunlid, Anders.

2012. Poster session presented at SMBE 2012 – Annual Meeting of the Society for Molecular Biology and Evolution, Dublin, Ireland.

Research output: Contribution to conferencePosterResearchpeer-review

Harvard

de Fine Licht, HH & Tunlid, A 2012, 'Elucidating the genetic landscape of cellular morphogenesis in an obligate fungal symbiont', SMBE 2012 – Annual Meeting of the Society for Molecular Biology and Evolution, Dublin, Ireland, 23/06/2012 - 26/06/2012.

APA

de Fine Licht, H. H., & Tunlid, A. (2012). Elucidating the genetic landscape of cellular morphogenesis in an obligate fungal symbiont. Poster session presented at SMBE 2012 – Annual Meeting of the Society for Molecular Biology and Evolution, Dublin, Ireland.

Vancouver

de Fine Licht HH, Tunlid A. Elucidating the genetic landscape of cellular morphogenesis in an obligate fungal symbiont. 2012. Poster session presented at SMBE 2012 – Annual Meeting of the Society for Molecular Biology and Evolution, Dublin, Ireland.

Author

de Fine Licht, Henrik Hjarvard ; Tunlid, Anders. / Elucidating the genetic landscape of cellular morphogenesis in an obligate fungal symbiont. Poster session presented at SMBE 2012 – Annual Meeting of the Society for Molecular Biology and Evolution, Dublin, Ireland.1 p.

Bibtex

@conference{4d68b71ac46c43d3a4ad7675631edf2f,
title = "Elucidating the genetic landscape of cellular morphogenesis in an obligate fungal symbiont",
abstract = "Fungi are masters of evolutionary adaptation, which have led to their enormous diversification and utilization as chemical factories of many potent secondary metabolites. Indeterminate growth and the capacity to produce distinct cell types are important sources of variation in fungal development. However, it remains largely unknown how natural selection on the genome drives adaptation of cellular morphogenesis. In many obligate mutualistic interactions the strong, but often narrow, selection pressure for a specific form or function provides an ideal framework for studying the genomic basis for fungal development. Our research identifies the key genetic adaptations of symbiotic fungi cultivated by fungus-growing ants to better understand the underlying evolutionary forces shaping fungal morphogenesis. A sub-group of these fungi form a distinct morphological adaptation to the symbiosis, i.e. inflated hyphal tips, called gongylidia. These structures are preferentially eaten by the cultivating ants and serve both as nutrition and as a source of fungal enzymes. These enzymes are important for efficient degradation of the plant substrate the ants use as substrate for cultivating the fungus garden. Using transcriptome sequencing and expressional profiling (RNA-seq) we identify and compare signatures of structural and expressional genetic adaptation in the evolution of these unique fungal structures.",
author = "{de Fine Licht}, {Henrik Hjarvard} and Anders Tunlid",
note = "Awarded 1st prize postdoctoral poster competition; null ; Conference date: 23-06-2012 Through 26-06-2012",
year = "2012",
language = "English",

}

RIS

TY - CONF

T1 - Elucidating the genetic landscape of cellular morphogenesis in an obligate fungal symbiont

AU - de Fine Licht, Henrik Hjarvard

AU - Tunlid, Anders

N1 - Awarded 1st prize postdoctoral poster competition

PY - 2012

Y1 - 2012

N2 - Fungi are masters of evolutionary adaptation, which have led to their enormous diversification and utilization as chemical factories of many potent secondary metabolites. Indeterminate growth and the capacity to produce distinct cell types are important sources of variation in fungal development. However, it remains largely unknown how natural selection on the genome drives adaptation of cellular morphogenesis. In many obligate mutualistic interactions the strong, but often narrow, selection pressure for a specific form or function provides an ideal framework for studying the genomic basis for fungal development. Our research identifies the key genetic adaptations of symbiotic fungi cultivated by fungus-growing ants to better understand the underlying evolutionary forces shaping fungal morphogenesis. A sub-group of these fungi form a distinct morphological adaptation to the symbiosis, i.e. inflated hyphal tips, called gongylidia. These structures are preferentially eaten by the cultivating ants and serve both as nutrition and as a source of fungal enzymes. These enzymes are important for efficient degradation of the plant substrate the ants use as substrate for cultivating the fungus garden. Using transcriptome sequencing and expressional profiling (RNA-seq) we identify and compare signatures of structural and expressional genetic adaptation in the evolution of these unique fungal structures.

AB - Fungi are masters of evolutionary adaptation, which have led to their enormous diversification and utilization as chemical factories of many potent secondary metabolites. Indeterminate growth and the capacity to produce distinct cell types are important sources of variation in fungal development. However, it remains largely unknown how natural selection on the genome drives adaptation of cellular morphogenesis. In many obligate mutualistic interactions the strong, but often narrow, selection pressure for a specific form or function provides an ideal framework for studying the genomic basis for fungal development. Our research identifies the key genetic adaptations of symbiotic fungi cultivated by fungus-growing ants to better understand the underlying evolutionary forces shaping fungal morphogenesis. A sub-group of these fungi form a distinct morphological adaptation to the symbiosis, i.e. inflated hyphal tips, called gongylidia. These structures are preferentially eaten by the cultivating ants and serve both as nutrition and as a source of fungal enzymes. These enzymes are important for efficient degradation of the plant substrate the ants use as substrate for cultivating the fungus garden. Using transcriptome sequencing and expressional profiling (RNA-seq) we identify and compare signatures of structural and expressional genetic adaptation in the evolution of these unique fungal structures.

M3 - Poster

Y2 - 23 June 2012 through 26 June 2012

ER -

ID: 119881115