We thank T. Smith and J. Krusky for technical assistance, and the Ontario Ministry of Agriculture and Food and the Ontario Bean Producers' Marketing Board for financial assistance. The cost of publishing this paper was defrayed in part by
M.E. Scott and T.E. Michaels
N.N. Wassimi, G.L. Hosfield, and M.A. Uebersax
Mich. Agr. Expt. Sta. Journal Article 13057. Research supported in part by a USAID/BIFAD bean/cowpea gram no. AID/DSAN-XII-G-0261. Mention of a trade name, proprietary product, or specific equipment does not constitute a guarantee or warranty by the
Paul Skroch and Jim Nienhuis
The genetic variation in a population of one hundred Snap Bean varieties, including processing and garden types, was studied using RAPD markers. All one hundred genotypes were distinguished by unique combinations of banding patterns. These unique “fingerprints” were tested for repeatability. Certain bands were very reliable and can be used for varietal identification. The RAPD marker data was also used to estimate genetic relationships among a subset of the one hundred lines. The results of the analysis agreed with known pedigree information. These markers will allow more precise monitering and control of germplasm by those who are involved with the breeding and production of superior seed.
Mario Crespo, James Nienhuis, Jan Tivang, and Paul Skroch
70 ORAL SESSION 19 (Abstr. 151–158) Breeding/Vegetable Crops I
Maricelis Acevedo Román, Albeiro Molina Castañeda, Juan Carlos Angel Sánchez, Carlos Germán Muñoz, and James S. Beaver
The inheritance of resistance to bean golden yellow mosaic virus (BGYMV) was studied in common beans (Phaseolus vulgaris L.). The original cross was made between breeding line PR9556-158, which produces deformed pods when infected with BGYMV, and PR9556-171, which has normal pod development when inoculated with the virus. Pod type was evaluated on plants from six generations (parental lines, F1, F2, F2:3, F3:4, and backcrosses of the F1 to both parents) at mid-pod fill (R8), ≈65 days after planting. The segregation patterns from the F2, F2:3, F3:4, and backcross populations were consistent with the hypothesis that a single dominant gene confers normal pod development in PR9556-171. When inoculated with BGYMV, the deformed pods of PR9556-158 produced fewer seeds per pod than PR9556-171, resulting in lower seed yield. The gene symbol Bgp-1 has been assigned for this dominant resistance gene that controls the normal pod reaction to BGYMV in common bean.
Mohamed F. Mohamed and Dermot P. Coyne
Pathology, for a Xcp bacterial isolate (V 4 S 1 ), and Kent Eskridge, Dept. of Biometry, Univ. of Nebraska, Lincoln, for statistical advice. We gratefully acknowledge the Title XII Bean/Cowpea Collaborative Research Support Program Project, Univ. of
Geunhwa Jung, Paul W. Skroch, Dermot P. Coyne, James Nienhuis, and E. Arnaud-Santana
106 POSTER SESSION (Abstr. 335–343) Breeding and Genetics–Vegetables II (Molecular Markers and Physiological Genetics)
Soon O. Park, Dermot P. Coyne, James R. Steadman, and Geunhwa Jung
White mold, incited by Sclerotinia sclerotiorum (Ss), is an important disease of common bean (Phaseolus vulgaris). Our objective was to identify RAPD markers and seedcoat pattern associated with QTL affecting resistance to Ss isolates 152 and 279 in a molecular marker-based linkage map previously constructed using a recombinant inbred (RI) population from the common bean cross `PC-50' (resistant to Ss) x XAN-159 (susceptible to Ss). White mold reactions were derived from a greenhouse straw test. Continuous distributions for the reactions to Ss isolates 152 and 279 were observed for RI lines, indicating quantitative inheritance. An intermediate (+0.67) Pearson correlation was observed between the reactions to Ss isolates 152 and 279. Low (0.24 and 0.23) narrow-sense heritabilities were found for the reactions to Ss isolates 152 and 279. Three QTL affecting resistance to Ss isolate 152 explained 33% of the phenotypic variation. Four QTL affecting resistance to Ss isolate 279 explained 54% of the phenotypic variation. The seedcoat pattern marker (C) on linkage group I was most consistently associated with resistance to Ss isolates 152 and 279, and explained 10% and 24% of the phenotypic variation for the traits, respectively. This is the first report on detection of QTL for white mold resistance in common bean. The RAPD markers and seedcoat pattern could be useful in breeding for white mold resistance.
Mark J. Bassett
The inheritance of corona and hilum ring color of common bean (Phaseolus vulgaris L.) was investigated in the reciprocal cross `Wagenaar' (a Canario market class dry bean) × `Mayocoba' (Mayocoba market class dry bean), where both parents were known to have seedcoat color genotype P [C r] gy J g b v lae Rk. `Wagenaar' has greenish yellow (GY) seedcoat (due to gy) except for purple (dark) corona (due to v lae) and reddish brown hilum ring (due to J), whereas `Mayocoba' has an entirely GY seedcoat. Seeds produced on the F1 progeny plants had GY corona and reddish brown hilum ring. The F2 segregated for three phenotypic classes, the two parental classes and the F1 class, but the segregation did not fit a 1:2:1 segregation ratio due to disturbed segregation. F3 progeny tests of 35 randomly selected F2 parents demonstrated that the two parental classes were true breeding and the F1 class segregated again (as in the F2) for the same three phenotypic classes. In spite of variable expressivity of GY color and disturbed segregation, the data support a single gene hypothesis, for which the tentative symbol Chr is proposed. Chr is dominant for changing purple corona to GY, but recessive for changing reddish brown hilum ring to GY. Thus, only one gene, Chr, controls the difference in seedcoat color between the market classes Canario and Mayocoba. An allelism test between Chr and Z (hilum ring color factor) is needed before a formal proposal for Chr can be made.
Jose J. Velez, Mark J. Bassett, James S. Beaver, and Albeiro Molina
The inheritance of resistance to bean golden mosaic virus (BGMV) in common bean (Phaseolus vulgaris L.) was studied in crosses between susceptible bean variety XAN176 and resistant breeding lines 9236-6 (T446/A429) and 9245-94 (DOR303/T968). Disease response data were taken on plants from four generations derived from each cross (parents, F1, F2, and backcrosses (BCs) of F1 to both parents) at 25 days after plants were inoculated with BGMV, using whiteflies (Bemisia argentifolii Bellows & Perring) as vectors. The segregation ratios obtained from F2 and BC generations were consistent with the hypothesis that resistance in 9236-6, which prevents a chlorotic response, is conferred by a single recessive gene. The disease response in 9245-94 was controlled by two genes—a dominant gene controlling a dwarfing reaction and a recessive resistance gene preventing a chlorotic response to BGMV infection. An allelism test demonstrated that the gene controlling resistance in 9236-6 is nonallelic with the recessive gene controlling resistance in 9245-94. The gene symbol bgm is proposed for the recessive resistance gene (originally from A429) in 9236-6. The gene symbol bgm-2 is proposed for the recessive resistance gene (originally from DOR303) in 9245-94.