Poster Display
Physiology, Biochemistry, and Toxicology
Chan C. Heu
ORISE Postdoctoral researcher
USDA-ARS
Maricopa, Arizona
Kyle M. Benowitz
Arizona State University
Mesa, Arizona
Luciano M. Matzkin (he/him/his)
Professor
University of Arizona
Tucson, Arizona
Carson W. Allan
University of Arizona
Tucson, Arizona
Dannialle M. LeRoy
USDA-ARS
Maricopa, Arizona
Xianchun Li, Ph.D. (he/him/his)
Professor
University of Arizona
Tucson, Arizona
Yves Carriere
Professor
University of Arizona
Tucson, Arizona
Bruce E. Tabashnik (he/him/his)
Regents Professor & Department Head
University of Arizona
Tucson, Arizona
Jeffrey A. Fabrick (he/him/his)
Research Entomologist
USDA-ARS
Maricopa, Arizona
Genetically engineered crops producing insecticidal proteins derived from Bacillus thuringiensis (Bt) are critical for management of some key insect pests. However, the evolution of resistance by pests has reduced the effectiveness of Bt crops. Helicoverpa zea (Lepidoptera: Noctuidae), one of the most damaging pests of crops in the U.S., has evolved widespread practical resistance to crops producing Bt crystalline (Cry) proteins including Cry1Ac. Understanding of the genetic basis of H. zea resistance to Cry1Ac has remained elusive. We previously used a genome-wide association study and fine-scale mapping to identify a premature stop codon in a kinesin-12 gene associated with Cry1Ac resistance in the lab-selected H. zea strain, GA-R. Here, we used CRISPR/Cas9 gene editing to modify the kinesin-12 gene. The results provide direct evidence that this gene affects susceptibility to Cry1Ac. These results also illustrate the power of pairing modern genomics and gene editing tools to better understand the genetic basis for resistance to Bt insecticidal proteins.