Location: Crop Improvement and Genetics Research2018 Annual Report
The long-term goal of this project is to develop useful biotechnology tools that enable the effective and precise genetic improvement of crop plants. Specifically, during the next five years we will focus on the three following objectives: Objective 1: Generate new molecular tools and new genetic strategies for effectively introducing and pyramiding multiple disease defense genes into citrus and potato to combat Huánglóngbìng and Zebra Chip diseases along with other priority traits. Objective 2: Identify and characterize new transcriptional control sequences (promoters and terminators) chosen for the precise control of gene transcription (tissue and/or developmental/environmental specificity) in crop plants containing single or multiple transgenes. Objective 3: Develop new methods that permit ARS biotechnology tools to be used for germplasm improvement in prioritized target crops and varieties. Subobjective 3A: Examine the capacity of the GAANTRY gene stacking system to enable the assembly and transfer of large arrays of sequences into transgenic plants. Subobjective 3B: Design and deploy a site-specific recombinase system that enables targeted transgene integration and marker removal in crop plants.
Candidate plant defense response genes will be introduced into potato and citrus plants using established methods for Agrobacterium–mediated transformation. The defense genes will either be constitutively expressed throughout the plant or expressed specifically in the phloem, the site of infection. Ten or more independent events for each candidate defense gene will have their susceptibility to zebra chip (in potato) or Huánglóngbìng (in citrus) evaluated. Candidate promoters with useful cell-type/organ expression specificities will be identified from crop plants. The candidate promoters will be fused to a reporter gene and transformed into rice, using Agrobacterium and/or other established transformation methods. Novel transcription terminator sequences will also be isolated from crop plants and fused to a reporter gene. The functionality of these promoter and terminator testing constructs will be examined in transient expression assays and stably transformed transgenic plants. Reporter gene expression levels will be quantitatively measured in major organs and compared to identify the sequences that provide the highest levels of transgene products while preserving promoter expression specificity. Plant molecular biological techniques will be used to further develop sophisticated biotechnology tools and methods for the improvement of crops. Transformation constructs of various large sizes (greater than 20 kilo base pairs) will be assembled using the site-specific recombinase-based GAANTRY gene stacking system. These constructs will be evaluated for their stability in bacteria and used to generate transgenic plants. The resulting genetically engineered plants will be molecular characterized to determine the effective capacity of the gene stacking technology. In parallel, technology enabling targeted integration and precise marker removal in transgenic plants will be developed and evaluated. “Exchange” T-DNA vectors will be constructed and transformed into “target” transgenic plants. Selection and molecular screening will be used to identify plants in which the incoming DNA has replaced the original transgenic locus (Recombinase-Mediated Cassette Exchange or RMCE). The efficiencies of different combinations of the unidirectional recombinases in performing RMCE will be compared.
This project just began March 26, 2018 and continues research from projects 2030-21000-020-00D, "Molecular Tools for Improved Crop Biotechnology" and 2030-21220-001-00D, "Host-Specific Molecular Genetic Tools for Development of Disease-Resistant Crops". The resources, funding and staff, were combined into this new five-year research project. Please see the annual reports for the previous projects for more information. Design of new transgenes and transformations have begun to evaluate the load capacity of the GAANTRY gene-stacking technology system. Potential citrus greening and zebra chip disease-resistance genes will be added to the potato and citrus genome during this process.
1. New molecular tools patented for improved crop development. Development of new molecular tools is an essential element of molecular breeding. ARS scientists in Albany, California, have successfully developed critical regulatory elements for the tissue specific expression. This is useful for disease-resistance genes as well as other beneficial genes directed towards crop improvement in citrus and in other species. U.S. Patent No. 10,047,369, "Citrus derived transcription and translation regulatory elements for tissue specific expression", was issued on August 14, 2018.
Collier, R., Thomson, J.G., Thilmony, R.L. 2018. A versatile and robust Agrobacterium-based gene stacking system generates high quality transgenic Arabidopsis plants. Plant Journal. 95(4):573-583. https://doi.org/10.1111/tpj.13992.
Franco, J.V., Wang, Y., Huo, N., Ponciano, G.P., Colvin, H.A., McMahan, C.M., Gu, Y.Q., Belknap, W.R. 2018. Modular assembly of transposable element arrays by microsatellite targeting in the guayule and rice genomes. BMC Genomics. 19:271. https://doi.org/10.1186/s12864-018-4653-6.