Genetic mapping of resistance to Phomopsis seed decay in the soybean breeding line MO/PSD-0259 (PI562694) and Plant Introduction 80837.

Resistance to Phomopsis seed decay (PSD) in soybean (Glycine max [L.] Merr.) could provide dependable control of this important disease that affects seed quality. Studies have shown that single dominant genes that are allelomorphically different confer low levels of PSD in MO/PSD-0259 and PI 80837. The objectives of this research were to identify simple sequence repeat (SSR) markers linked to genes for PSD resistance in PI 80837 and MO/PSD-0259 and to associate the resistance genes to known linkage groups. Crosses were made between the PSD-susceptible cultivar Agripro 350 and each of the resistant lines MO/PSD-0259 and PI 80837. F(2) populations from each cross were grown and inoculated in the field. Individual plant reactions were characterized by determining the levels of seed infection, and DNA of F(2) plants was extracted for SSR analysis and mapping. F(2) segregation data showed that different single dominant genes condition PSD resistance in MO/PSD-0259 and PI 80837. Resistance in PI 80837 was linked to Sat_177 (4.3 cM) and Sat_342 (15.8 cM) on molecular linkage group (MLG) B2. In MO/PSD-0259, resistance was linked to Sat_317 (5.9 cM) and Sat_120 (12.7 cM) on MLG F. These data support work by Berger and Minor (Berger RD, Minor HC. 1999. An restriction fragment length polymorphism (RFLP) marker associated with resistance to Phomopsis seed decay in soybean PI 417479. Crop Sci 39:800-805.) in which PSD resistance in PI 417479, the resistant parent used to develop MO/PSD-0259, was associated with RFLP marker A708 on MLG F. These SSR markers should be useful in selection for resistant genotypes in breeding programs.

Inheritance of resistance to Phomopsis seed decay in PI 360841 soybean.

Phomopsis longicolla Hobbs is the primary cause of Phomopsis seed decay (PSD) in soybean. Infection may result in moldy seed and poor germination. The objective of this study was to conduct inheritance studies to characterize resistance to PSD in plant introduction (PI) 360481. Crosses were made between PI 360841 and 2 PSD-susceptible genotypes, Agripro (AP) 350 and PI 91113, to determine the number of genes for resistance. Additionally, crosses were made between PI 360841 and Phomopsis resistant parents MO/PSD-0259 and PI 80837 to test the allelism of the resistance genes. Seed infection assays were done using seed from parent plants and F(2) populations. Chi-square analysis of the resistant x susceptible F(2) data fit to a 9R:7S model for 2 complementary dominant genes conferring PSD resistance in PI 360841. Segregation for reaction in the F(2) of MO/PSD-0259 x PI 360841 exhibited a good fit to a 57R:7S model for 2 complementary dominant genes from PI 360841 and a different dominant gene from MO/PSD-0259. There was no apparent segregation in the F(2) population from PI 360841 x PI 80837 except for one suspicious susceptible plant, suggesting one of the genes in PI 360841 is the same gene in PI 80837 for PSD resistance.

Genetic mapping of resistance to purple seed stain in PI 80837 soybean.

Purple seed stain (PSS) of soybean caused by Cercospora kikuchii is an important disease that reduces market grade and can affect seed germination and vigor. A single dominant gene was shown to confer PSS resistance in PI 80837. The objective of this research was to map the PSS resistance gene in PI 80837 using simple sequence repeat (SSR) markers. A cross was made between the PSS-susceptible cultivar Agripro 350 (AP 350) and PI 80837. The F2 population and parents were grown in the field, and the resistance or susceptibility of individual plants was determined by assaying the seed for infection by C. kikuchii. DNA of parent and F2 plants was extracted for SSR analysis and mapping. Segregation ratios for seed infection and for SSR markers showed that a single dominant gene conditions resistance to PSS in PI 80837. The candidate resistance gene was mapped between Sat_308 (6.6 cM) and Satt594 (11.6 cM) on molecular linkage group G. These markers may be useful in marker-assisted selection for utilizing PSS resistance from PI 80837 in a breeding program.