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35th NPS abstract book

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P37<br />

Unraveling the polyploid origin of coast redwood (Sequoia sempervirens)<br />

with Bayesian concordance analysis<br />

A. D. SCOTT, N. STENZ and D. A. BAUM<br />

Department of Botany, University of Wisconsin - Madison, 430 Lincoln Drive, Madison, WI 53706,<br />

USA<br />

Coast redwood (Sequoia sempervirens) stands out as not only one of the tallest, longest-lived trees,<br />

but as the only hexaploid conifer. As whole genome duplication is rare in gymnosperms, a better<br />

understanding of the causes of polyploidy in Sequoia may clarify why polyploidy has played a<br />

relatively minimal role in gymnosperm evolution. We sequenced transcriptomes from Sequoia,<br />

Sequoiadendron, and Metasequoia, and estimated phylogenetic trees for 3,605 genes. Bayesian<br />

concordance analysis of 3,045 low-copy genes suggests Sequoiadendron is the closest relative of<br />

Sequoia for ~80% of the genome. Gene trees with multiple homeologs in coast redwood consistently<br />

show monophyly of those homeologs. This suggests that hexaploidy is a result of autopolyploidy or,<br />

that if hybridization did occur, it involved only species that are more closely related to Sequoia than<br />

either Sequoiadendron or Metasequoia. Our analyses suggest a polyploid origin for Sequoia ~24 mya<br />

(homeolog divergence at K s ~ 0.0168), in apparent contradiction to the fossil record.<br />

P38<br />

Who’s who? Finding the CESA genes in White Spruce encoding the secondary<br />

wall specific cellulose synthase<br />

I. DUVAL 1 , D. LACHANCE 1 , I. GIGUÈRE 2 , M-J. MORENCY 1 , G. PELLETIER 1 , J. J. MACKAY 2, 3 and A.<br />

SÉGUIN 1*<br />

1 Natural Resources Canada, Laurentian Forestry Centre, Québec QC G1V 4C7, Canada; 2 Centre<br />

d’Étude de la Forêt, Université Laval, Québec (QC), G1V A06, Canada; 3 Department of Plant Sciences,<br />

University of Oxford, Oxford, OX1 2RB, UK<br />

Phylogenetic analyses of CESA genes have shown specific divergence within the gene family for<br />

either primary or secondary wall development. In Picea glauca (white spruce) the PgCESA3 gene has<br />

been principally associated to developing xylem. Tissue specific gene expression analyses using a<br />

PgCESA3 promoter-GUS reporter construct revealed localised expression associated to secondary<br />

wall formation. We also obtained evidences that specific spruce MYB transcription factors are<br />

implicated in the regulation of PgCESA3 gene promoter by using a tissue culture based system and a<br />

transactivation approach. Furthermore, using electrophoretic mobility shift assay (EMSA) we<br />

confirmed that PgMYB12 directly binds in vitro to the PgCESA3 promoter. Overall, functional<br />

genomic tools and global expression data for white spruce is a powerful assets for delineating the<br />

evolution and dynamics of complex gene families such as CESA.<br />

51

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