Disease resistance alleles in soybean
Methods for conveying Phytophthora sojae resistance into non-resistant soybean germplasm are provided. In some embodiments, the methods include introgressing Phytophthora sojae resistance into a non-resistant soybean using one or more nucleic acid markers for marker-assisted breeding among soybean lines to be used in a soybean breeding program, wherein the markers are linked to and/or associated with Phytophthora sojae resistance. Also provided are single nucleotide polymorphisms (SNPs) associated with resistance to pathogens; soybean plants, seeds, and tissue cultures produced by any of the disclosed methods; seed produced by the disclosed soybean plants; and compositions including amplification primer pairs capable of initiating DNA polymerization by a DNA polymerase on soybean nucleic acid templates to generate soybean marker amplicons to be used in selecting or identifying Phytophthora sojae resistant soybean lines.
1. A soybean plant having in its parental pedigree a plant selected based on the presence of a marker associated with phytophthora tolerance in a soybean plant, wherein said marker is located within a chromosomal interval on chromosome 13 including at least one of
a G allele corresponding to position 404 of SEQ ID NO: 1,
a G allele corresponding to position 495 of SEQ ID NO: 2, and a deletion corresponding to position 499 of SEQ ID NO: 3.
2. The plant of claim 1 , wherein said chromosomal interval includes a G allele corresponding to position 404 of SEQ ID NO: 1, and a G allele corresponding to position 495 of SEQ ID NO: 2.
3. The plant of claim 1 , wherein said chromosomal interval includes a G allele corresponding to position 404 of SEQ ID NO: 1, and a deletion corresponding to position 499 of SEQ ID NO: 3.
4. The plant of claim 1 , wherein said chromosomal interval includes a G allele corresponding to position 495 of SEQ ID NO: 2 and a deletion corresponding to position 499 of SEQ ID NO: 3.
5. The plant of claim 1 , wherein said chromosomal interval includes each of a G allele corresponding to position 404 of SEQ ID NO: 1, a G allele corresponding to position 495 of SEQ ID NO: 2, and a deletion corresponding to position 499 of SEQ ID NO: 3.