Bioinformatics Seminar

An occasional seminar series on bioinformatics, at Berkeley and beyond!

Title: High Quality Datasets to Provision Fungal Genomics Journeys

Speaker: Amy J. Powell, Ph.D, Fungal Genomics Laboratory, North Carolina State University

Time: 10am-11am, Thursday, September 13th, 2007

Place: 338 Koshland Hall

Abstract:
The role of differential gene gain and/or loss remains largely unexamined in the context of fungal pathogenesis, particularly on a genomic scale, despite its known relevance to virulence in bacteria and viruses. To embark on a genome-wide analysis, the gene families for eleven sequenced fungal genomes were inventoried to discern whether patterns of gene duplication, a common mechanism for gene gain, were distinct in pathogens versus non-pathogens. This analysis included nine Ascomycete species, and two Basidiomycete lineages. We developed a semi-automated high-throughput computational platform, FEGA (Fungal Evolutionary Genome Analyses) to facilitate large-scale comparative studies to explore evolutionary patterns associated with fungal pathogenesis. This platform is comprised of tools and a database that currently contains gene family assignments, Gene Ontology (GO)-based annotations, gene co-ordinates, as well as selection and divergence indices. Our platform was engineered to facilitate extension. Overall, the distribution of gene family sizes was not distinct in pathogens, as compared to non-pathogens. However, phylogenetically informed comparisons revealed several instances where fungal pathogens showed globally altered patterns of gene duplication, as indicated by differences in gene family size distribution. Genome-wide surveys of gene family dynamics revealed eighteen possible examples of gene family expansion, as well as eight instances of gene family contraction in pathogenic lineages. Examples of gene families showing expansion in pathogens included those known to be important in insect exoskeleton or plant host cell wall modification (e.g., chitin deacetylase, cutin hydrolase, endoglucanase, feruloyl esterase). Instances of contracted gene families included those with vacuolar ATP synthase and alcohol dehydrogenase function. Pairwise species comparisons revealed additional instances of expanded gene families. A survey of the functional distribution of gene duplicates indicated that pathogens, globally, showed enrichment for duplicates associated with receptor and hydrolase activities, and Ascomycete pathogens appear to have not only these differences, but also significantly more duplicates associated with regulatory and carbohydrate binding functions. The observed functional differences possibly have adaptive value for pathogens, and likely reflect ancient, as well as contemporary intimate associations with a host.



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