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Research Project: High Through-Put SNP Genotyping of the USDA Pea Core Collection

Location: Plant Germplasm Introduction and Testing

Project Number: 5348-21000-028-09
Project Type: Specific Cooperative Agreement

Start Date: Sep 12, 2012
End Date: Jul 31, 2013

Objective:
The expected objective is an association mapping panel of 384 pea accessions genotyped for 20,000-plus SNPs based on genotyping-by-sequencing of the highly phenotyped pea core germplasm collection. The pea core population has been evaluated extensively for a variety of agronomic and morphological traits – seed weight, disease and pest resistances, stem and root traits, protein and macronutrient seed concentrations (Jermyn and Slinkard 1977; Kraft et al., 1998; Tedford and Inglis 1999; McPhee and Muehlbauer 1999, 2001; Malvick and Percich 1999; McPhee et al., 1999; Grunwald et al., 2003; Grusak et al., 2004, McPhee 2005; Coyne et al., 2005a). This high density genotyped panel can then be used for genome-wide association studies (GWAS) as demonstrated in a spring barley germplasm collection (Pasam et al., 2012) and for genomic selection (Heffner et a., 2010). This germplasm panel will be a valuable community resource (Mackey et al 2012). This pea core has been expanded from the refined pea core (Coyne et al 2005b) with the addition of Pisum subspecies, RIL mapping population parents, and snap pea lines.

Approach:
1. The pea core population (384 accessions-adjusted with entries from Jim Myers) will be grown in the greenhouse. Leaf samples will be collected and DNA extracted into four 96-cell format plates using the Qiagen DNeasy kit. DNA concentrations will be determined using a fluorometer. Yields: 100 µl of 300-500 ng/µl DNA. 2. DNA plates will be shipped to the Institute for Genomic Diversity at Cornell University for sequencing. 3. Preparation of libraries for Next-Generation Sequencing (Elshire et al., 2011). Figure 1 shows the genotyping-by-sequencing (GBS) adaptors. A basic schematic of the protocol to be used for performing GBS is shown in Figure 2. Sequencing will be performed using Genome Analyzer II (Illumina, Inc., San Diego, CA) or similar. Raw sequence data is filtered, the DNA sequence aligned using The Basic Local Alignment Search Tool (BLAST) and SNPs called.

   

 
Project Team
Coyne, Clarice - Clare
McGee, Rebecca
 
Related National Programs
  Plant Genetic Resources, Genomics and Genetic Improvement (301)
 
 
Last Modified: 05/22/2013
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