January 14-18, 2006
Town & Country Convention Center
San Diego, CA
Daniel G. Peterson1,2 , C. Dana Nelson2,3 , M. Nurul Islam-Faridi3,4 , Doreen S. Main5,6 , Jeffrey P. Tomkins5 , Annita Avery7 , John E. Carlson8 , Philippe Chouvarine1,2 , Zenaida V. Magbanua1,2 , Dipaloke Mukherjee1,2 , LaShonda Robertson7 , Surya Saha1 , Supaphan Thummasuwan1,2
We are working to establish a better understanding of the genome of loblolly pine, Pinus taeda L., the most economically important tree in the U.S. Deliverables of this project, now starting its second year, include a 10X BAC library for the loblolly genotype "7-56," characterization of the pine genome via Cot analysis, sequencing of random genomic and Cot-filtered sequences, and study of the organization of repetitive and low-copy sequences by fluorescence in situ hybridization (FISH) and macroarray analysis. Collectively, the data generated in this study will provide considerable insight into the structure of the pine genome which in turn will help guide efficient physical mapping and sequencing of pine. To date, high-throughput archival of BAC clones is well underway, Cot analysis has been completed, and Cot-filtered libraries are under construction. With regard to sequencing, a new partnership with John Carlson (Pennsylvania State University) and minor re-budgeting has provided us with an opportunity to utilize a 454 Genome Sequencer 20 (www.454.com) to produce > 20 times the sequence data slated for generation in the original funded proposal. The 454 sequence data will be compared with genomic and Cot-filtered sequences elucidated using standard capillary sequencing techniques. The > 60 Mb of sequence data produced to date and the growing BAC library have set the stage for the FISH- and macroarray-based physical mapping of the pine genome slated to begin in Year 2. Additional information on this project is available at www.mgel.msstate.edu.