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National Science Foundation Research Coordination Networks in Biology Oomycete Genomics Research Collaboration Network 2007-2013 USDA NIFA Oomycete Coordinated Agricultural Project Integrated management of oomycete diseases of soybean and other crop plants 2011-2016 Funding Acknowledgements
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Page 1: Genomics and functional dynamics of effector genesoomycete-training.org/wp-content/uploads/2014/04/tyler-overview-ppt.pdfRapidly diverging RXLR superfamily in Oomycetes P. sojae ~400

• National Science Foundation

– Research Coordination Networks in Biology

– Oomycete Genomics Research Collaboration Network

– 2007-2013

• USDA NIFA

– Oomycete Coordinated Agricultural Project

– Integrated management of oomycete diseases of soybean and other crop plants

– 2011-2016

Funding Acknowledgements

Page 2: Genomics and functional dynamics of effector genesoomycete-training.org/wp-content/uploads/2014/04/tyler-overview-ppt.pdfRapidly diverging RXLR superfamily in Oomycetes P. sojae ~400

Oomycete Genomics, Past, Present and Future

Brett Tyler

Center for Genome Research and BiocomputingOregon State University

and

Virginia Bioinformatics InstituteVirginia Polytechnic Institute and State University

Page 3: Genomics and functional dynamics of effector genesoomycete-training.org/wp-content/uploads/2014/04/tyler-overview-ppt.pdfRapidly diverging RXLR superfamily in Oomycetes P. sojae ~400

Oomycetes and Genome Sequencing

ultimum

plant pathogens

animal pathogens

Page 4: Genomics and functional dynamics of effector genesoomycete-training.org/wp-content/uploads/2014/04/tyler-overview-ppt.pdfRapidly diverging RXLR superfamily in Oomycetes P. sojae ~400

alfalfaalmondappleapricotavocadoazaleabananabean (Phaseolus)blackberryblueberryBrassicacabbagecacaocanolacantaloupecarnationcauliflowercedarchestnutchickpeacitrusclovercoconutcoffeecottoncowpeacranberrycucurbitsdate palm egg planteucalyptusfirguavahibiscushops

larchmacadamiamelonmustardoakoil palmpapayapassionfruitpea (Pisum)peachpearpecanpepperperiwinklepinepineapplepistachioplumpomegranatepotatopumpkinraspberryrhododendronsafflowersesamesoybeansquashstrawberrysugar beetsunflowertobaccotomatoviburnumwalnutzucchini

PhytophthoraGenome

Sequencing

Some Phytophthora hosts

Sequenced

In progress

> 120 destructive pathogen species

Page 5: Genomics and functional dynamics of effector genesoomycete-training.org/wp-content/uploads/2014/04/tyler-overview-ppt.pdfRapidly diverging RXLR superfamily in Oomycetes P. sojae ~400

alfalfaalmondappleapricotavocadoazaleabananabean (Phaseolus)blackberryblueberryBrassicacabbagecacaocanolacantaloupecarnationcauliflowercedarchestnutchickpeacitrusclovercoconutcoffeecottoncowpeacranberrycucurbitsdate palm egg planteucalyptusfirguavahibiscushops

larchmacadamiamelonmustardoakoil palmpapayapassionfruitpea (Pisum)peachpearpecanpepperperiwinklepinepineapplepistachioplumpomegranatepotatopumpkinraspberryrhododendronsafflowersesamesoybeansquashstrawberrysugar beetsunflowertobaccotomatoviburnumwalnutzucchini

PhytophthoraGenome

Sequencing

Some Phytophthora hosts

Sequenced

In progress

> 120 destructive pathogen species

New initiative with BGI(eventually all species)

Page 6: Genomics and functional dynamics of effector genesoomycete-training.org/wp-content/uploads/2014/04/tyler-overview-ppt.pdfRapidly diverging RXLR superfamily in Oomycetes P. sojae ~400

Oomycete Genome Comparisons

• P. sojae vs P.ramorum vs P. infestans– ~9,800 orthologs (highly conserved genes with same functions)

– 45-55% of genome orthologous

– 25-45% in recognizable gene families

– ~10% unique

– many genes for attacking plant tissue

• Saprolegnia parasitica– ~8400 orthologs

– many more introns

– more compact genome, fewer repetitive sequences

– many genes for attacking animal tissues

Page 7: Genomics and functional dynamics of effector genesoomycete-training.org/wp-content/uploads/2014/04/tyler-overview-ppt.pdfRapidly diverging RXLR superfamily in Oomycetes P. sojae ~400

Conserved gene order within the Peronosporales

Phytophthora infestanssupercontig1.1Haas et al 2009

Pythium ultimum

scf1117875581354

Levesque et al 2010

Hyaloperonospora arabidopsidisscaffolds 9; 126; 7; 47Baxter et al 2010

Phytophthora ramorumscaffold_1Tyler et al 2006

PHRINGE analysis: Jeff Boore

Page 8: Genomics and functional dynamics of effector genesoomycete-training.org/wp-content/uploads/2014/04/tyler-overview-ppt.pdfRapidly diverging RXLR superfamily in Oomycetes P. sojae ~400

Effector genes are associated with repeat rich regions in oomycete genomes

Haas et al (2009) Nature 461(7262): 393-399

Page 9: Genomics and functional dynamics of effector genesoomycete-training.org/wp-content/uploads/2014/04/tyler-overview-ppt.pdfRapidly diverging RXLR superfamily in Oomycetes P. sojae ~400

Necrosis = death: effect of P.sojae NIP

Protein toxin genes have expanded subsequent to speciation the NPP1 family Credit: Mark Gijzen

Qutob et al Plant J. 32, 361, 2002

P. sojaeP. ramorum

Page 10: Genomics and functional dynamics of effector genesoomycete-training.org/wp-content/uploads/2014/04/tyler-overview-ppt.pdfRapidly diverging RXLR superfamily in Oomycetes P. sojae ~400

Rapidly diverging RXLR superfamily in Oomycetes

P. sojae ~400P. ramorum ~370P. infestans ~550H. arabidopsidis ~130

Signal Peptide RXLR dEER

27aa10-67aa

14aa7-55aa

126aa28-835aa

medianrange

Includes 16/17 cloned oomycete avirulence genesPsAvr1a, PsAvr1b, PsAvr1k, PsAvr3a,PsAvr3b, PsAvr3c, PsAvr4/6, PsAvr5PiAvr1, PiAvr2,PiAvr3a, PiAvr4, PiAvrPlb1/ipiO1, PiAvrPlb2, HaAtr1, HaAtr13HaAtr5Jiang et al PNAS

105(12), 4874-4879 (2008)

Page 11: Genomics and functional dynamics of effector genesoomycete-training.org/wp-content/uploads/2014/04/tyler-overview-ppt.pdfRapidly diverging RXLR superfamily in Oomycetes P. sojae ~400

Integration of Oomycete & Fungal Database Resources

FungiDB

www.FungiDB.org

DOE JGI Mycocosm

http://genome.jgi-psf.org/programs/fungi/index.jsf

VMD vmd.vbi.vt.edu

EumicrobeDB.org


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