Research article
Complementary genetic and genomic approaches help characterize the linkage group I seed protein QTL in soybean
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* Corresponding author: Carroll P Vance vance004@umn.edu
- † Equal contributors
1 United States Department of Agriculture-Agricultural Research Service, Plant Research Unit, St Paul, MN 55108, USA
2 Department of Agronomy, Iowa State University, Ames, IA 50011, USA
3 United States Department of Agriculture-Agricultural Research Service, Corn Insects and Crop Genetics Research Unit, Ames, IA 50011, USA
4 Department of Crop Sciences, University of Illinois, 1101 West Peabody Dr, Urbana, IL 61801, USA
5 National Center for Genome Resources, Santa Fe, NM 87505, USA
6 Department of Agronomy and Plant Genetics, University of Minnesota, St Paul, MN 55108, USA
7 Department of Agronomy, University of Nebraska, Lincoln, NE 68583, USA
8 Minnesota Supercomputing Institute, University of Minnesota, Minneapolis, MN 55455, USA
BMC Plant Biology 2010, 10:41 doi:10.1186/1471-2229-10-41
Published: 3 March 2010Abstract
Background
The nutritional and economic value of many crops is effectively a function of seed protein and oil content. Insight into the genetic and molecular control mechanisms involved in the deposition of these constituents in the developing seed is needed to guide crop improvement. A quantitative trait locus (QTL) on Linkage Group I (LG I) of soybean (Glycine max (L.) Merrill) has a striking effect on seed protein content.
Results
A soybean near-isogenic line (NIL) pair contrasting in seed protein and differing in an introgressed genomic segment containing the LG I protein QTL was used as a resource to demarcate the QTL region and to study variation in transcript abundance in developing seed. The LG I QTL region was delineated to less than 8.4 Mbp of genomic sequence on chromosome 20. Using Affymetrix® Soy GeneChip and high-throughput Illumina® whole transcriptome sequencing platforms, 13 genes displaying significant seed transcript accumulation differences between NILs were identified that mapped to the 8.4 Mbp LG I protein QTL region.
Conclusions
This study identifies gene candidates at the LG I protein QTL for potential involvement in the regulation of protein content in the soybean seed. The results demonstrate the power of complementary approaches to characterize contrasting NILs and provide genome-wide transcriptome insight towards understanding seed biology and the soybean genome.