W196
Associating Phenotype to Genotype in Lettuce Using NGS, in silico Analyses, High Resolution Genetic Maps and Targeted Fine Mapping

Date: Tuesday, January 13, 2015
Time: 1:50 PM
Room: Pacific Salon 4-5 (2nd Floor)
Dean Lavelle , Genome Center, University of California, Davis, CA
Sebastian Reyes Chin-Wo , Genome Center, University of California, Davis, CA
Alexander Kozik , Genome Center, University of California, Davis, CA
Maria Jose Truco , Genome Center, University of California, Davis, CA
Lutz Froenicke , Genome Center, University of California, Davis, CA
Marilena Christopoulou , Genome Center, University of California, Davis, CA
Angel Fernandez i Marti , Genome Center, University of California, Davis, CA
Miguel Macias González , Genome Center, University of California, Davis, CA
Carolina Font i Forcada , Genome Center, University of California, Davis, CA
Huaqin Xu , Genome Center, University of California, Davis, CA
Richard Michelmore , Genome Center, University of California, Davis, CA
The genome of cultivated lettuce (L. sativa cv. Salinas) has been sequenced in collaboration with BGI and a consortium of ten breeding companies. The assembly currently consists of 21,500 scaffolds totaling 2.38 Gb and representing 88% of the 2.7 Gb lettuce genome.  Annotation of the reference genome of L. sativa now contains 39,000 high confidence gene models based on an overlapping weighted evidence gene model scoring method (OWEG score) that combines transcriptomic and prediction evidence. More than 12 million high quality SNPs were identified between L. sativa cv. Salinas and L. serriola acc. US96UC23 and used to construct an ultra-dense genetic map using a RIL population derived from L. sativa x L. serriola. Segregation analysis of scaffold haplotypes assigned over 96% of the assembled genome to genetic bins ordered along the nine chromosomal linkage groups. Additional sequencing has provided six new de novo genome assemblies of L. sativa (Valmaine, La Brillante, Diana, Greenlake, PI251246, and Iceberg) as well as low-pass sequencing of 16 additional genotypes (L. sativa and L. serriola). The ultra-dense map has facilitated genetic dissection and mapping of domestication and agriculturally important loci. QTLs are being fine mapped using RILs containing residual heterozygosity  at QTL regions. Recombinants at these QTL regions are being characterized using next-gen sequencing to identify candidate genes.