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Message - 7th IAL Symposium

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The 7 th International Association for Lichenology <strong>Symposium</strong> 2012<br />

1B: Genomic approaches to studying the lichen symbiosis<br />

(1B-O1) Submission ID: <strong>IAL</strong>0319-00001<br />

APPROACHING LICHENS BY UNWINDING COMPLEMENTARY GENOMES:<br />

AN INTRODUCTION<br />

Miao V. 1 , Armaleo D. 2<br />

1 Department of Microbiology and Immunology, University of British Columbia, Vancouver, Canada<br />

2 Department of Biology, Duke University, Durham, United States<br />

Lichen symbionts are unique in their near-absolute dependence on each other in nature, accompanied<br />

by occasional streaks of independence most obvious in aposymbiotic culture. This session will look at this<br />

balancing act from a genomics perspective. Superficially, the symbionts’ genomes are not very different from<br />

those of their non-symbiotic fungal and algal relatives. They have not degenerated so as to produce absolute<br />

dependence between mycobiont and photobiont, but have evolved in subtle ways to cement an intimate and<br />

successful interaction while maintaining each partner’s individuality. We will look not only at the general structure<br />

of several lichen genomes, but also at features connected with their functioning in the symbiosis: changes in<br />

gene families, presence of genes unique to lichens, transcriptional adaptations, metabolic adaptations, epigenetic<br />

changes. We will survey the mycobiont of Xanthoria parietina, two closely related Peltigera species and<br />

their cyanobionts, Cladonia grayi and its Asterochloris sp. photobiont, horizontal gene transfer in Trebouxia, and<br />

the effect of different ecological conditions on the larger bacterial communities inhabiting various lichens.<br />

(1B-O2) Submission ID: <strong>IAL</strong>0293-00001<br />

GENOME SEQUENCING OF XANTHORIA PARIETINA 46-1-SA22<br />

Dyer P. S. 1 , Crittenden P. D. 1 , Archer D. B. 1 , Barry K. 2 , Foster B. 2 , Copeland A. 2 , Kuo A. 2 , Grigoriev I. 2<br />

1 School of Biology, University of Nottingham, Nottingham, United Kingdom<br />

2 Eukaryotic Genome Program, DOE Joint Genome Institute, Walnut Creek, United States<br />

Xanthoria parietina has been chosen as a representative lichen-forming fungus for genome sequencing.<br />

This species was nominated because it has a wide distribution (being found in temperate and circumpolar<br />

regions worldwide), has a characteristic stratified thallus morphology, is amenable to axenic cultivation, and is<br />

one of the most commonly studied lichenized fungi. It can occur on a variety of substrata including rock, tree<br />

bark and man-made surfaces. To enable genome studies, ascospore progeny from an individual thallus of X.<br />

parietina were collected from the Peak District, UK, and grown in axenic culture to allow extraction of DNA purely<br />

of the fungal mycobiont. Sequencing of the genomic DNA by 454 and Illumina pyrosequencing technology has<br />

now been completed at the DOE Joint Genome Institute. Preliminary analysis reveals a 32 Mbp size genome<br />

(typical of pezizomycete fungi) with an estimated 10,800 genes of average size 1,505 nt encoding an average<br />

protein length of 432 amino acids. In further work, mRNA samples are being extracted from both the symbiotic<br />

(field thallus) and non-symbiotic (axenic pure culture) states of X. parietina prior to library construction and whole<br />

transcriptome sequencing (“RNA seq”). Arising data will be used for training of the genome auto-annotation process,<br />

and it is anticipated that comparison of transcriptome pools will yield insights into differential regulation of<br />

genes in the symbiotic versus non-symbiotic state. A multinational genome annotation group has been set up to<br />

assist with the genome annotation and analysis.<br />

19<br />

1B-O

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