Tuesday, November 3, 2009: 11:30 AM
Convention Center, Room 402, Fourth Floor
Zhanguo Xin, PSGD, USDA-ARS, Lubbock, TX, Ming Li Wang, USDA-ARS, Plant Genetic Resources Conservation Unit, Griffin, GA, Gloria Burow, PSGD, CSRL, USDA-ARS, Lubbock, TX and John Burke, USDA-ARS, Lubbock, TX
Sorghum (Sorghum bicolor L. Moench)
is ranked as the fifth most important grain crop and serves
as a major food staple and fodder resource for much of the world, especially in
arid and semi-arid regions. The recent
surge in sorghum research is driven by its tolerance to drought / heat stresses
and its strong potential as a bioenergy
feedstock. Completion of the sorghum
genome sequence has opened new avenues for sorghum functional genomics. However, the availability of genetic
resources, specifically mutant lines, is limited. Chemical mutagenesis of sorghum germplasm,
followed by screening for mutants altered in important agronomic traits,
represents a rapid and effective means of addressing this limitation. A sorghum mutant population consisting of
1,600 lines was generated from the inbred line BTx623 by treatment with the
chemical agent ethyl methanesulfonate (EMS). Numerous
phenotypes with altered morphological and agronomic traits were observed from M2
and M3 lines in the field. A
subset of 768 mutant lines was analyzed by TILLING using four target
genes. A total of five mutations were
identified resulting in a calculated mutation density of 1/526 kb. Two of the mutations identified by TILLING
were verified by sequencing in the gene encoding caffeic
acid O-methyltransferase (COMT) in two independent mutant lines. The two mutant COMT lines segregate for the expected brown midrib (bmr) phenotype, a trait associated with
reduced lignin content and increased digestibility. The diversity of the mutant phenotypes
observed in the field, and the density of induced mutations calculated from
TILLING, indicate that this mutant population represents a useful resource for
sorghum genomic studies.