Search

The pinto bean (Phaseolus vulgaris L.) cultivar 'USDA Diamondback' (Reg. no. CV‐353, PI 698822) was released by the USDA‐ARS in 2022 as a high‐yielding cultivar with an upright architecture and the slow‐darkening seed coat trait. It was bred for tolerance to multiple abiotic stresses in a "purgatory" plot purposely managed to have compacted soil, low soil fertility, and intermittent drought conditions. Conversely, selection for high yield potential was conducted in non‐stress trials with tillage, irrigations, and fertilizers applied for optimal production. USDA Diamondback exhibits wide adaption to production regions across the United States, as evidenced by an average seed yield of 3808 kg ha−1 across 14 location‐years in the Cooperative Dry Bean Nursery. Virus testing and resistance gene–linked markers indicate USDA Diamondback has a three‐gene combination (bc‐ud, bc‐1, and bc‐3) that confers durable resistance to all known strains of Bean common mosaic virus and Bean common mosaic necrosis virus. A similar combination of pathogen and marker testing indicated that USDA Diamondback possesses the Ur‐3 and Ur‐6 genes for resistance to bean rust. The seed size, appearance, and canning quality characteristics of USDA Diamondback meets the industry standards for packaging and processing. Core Ideas: USDA Diamondback was bred for high yield potential under both favorable and stressful environments.USDA Diamondback has the slow‐darkening trait that maintains seed coat brightness during prolonged storage.USDA Diamondback has above‐average canning quality.USDA Diamondback is resistant to all known strains of Bean common mosaic virus and Bean common mosaic necrosis virus. [ABSTRACT FROM AUTHOR]

Background: Common beans (Phaseolus vulgaris L.) provide important protein and calories globally. Anthracnose (Colletotrichum lindemuthianum (Sacc. & Magnus) Briosi & Cavara, 1889) is a major disease in common bean and causes significant yield losses in bean production areas. Screening for markers linked to known disease resistance genes provides useful information for plant breeders to develop improved common bean varieties. The Kompetitive Allele Specific PCR (KASP) assay is an affordable genetic screening technique that can be used to accelerate breeding programs, but manual DNA extraction and KASP assay preparation are time-consuming. Several KASP markers have been developed for genes involved in resistance to bean anthracnose, which can reduce yield by up to 100%, but their usefulness is hindered by the labor required to screen a significant number of bean lines. Our research objective was to develop publicly available protocols for DNA extraction and KASP assaying using a liquid handling robot (LHR) which would facilitate high-throughput genetic screening with less active human time required. Anthracnose resistance markers were used to compare manual and automated results. Results: The 12 bean anthracnose differential cultivars were screened for four anthracnose KASP markers linked to the resistance genes Co-1, Co-3 and Co-42 both by hand and with the use of an LHR. A protocol was written for DNA extraction and KASP assay thermocycling to implement the LHR. The LHR protocol reduced the active human screening time of 24 samples from 3h44 to 1h23. KASP calls were consistent across replicates but not always accurate for their known linked resistance genes, suggesting more specific markers still need to be developed. Using an LHR, information from KASP assays can be accumulated with little active human time. Conclusion: Results suggest that LHRs can be used to expedite time-consuming and tedious lab work such as DNA extraction or PCR plate filling. Notably, LHRs can be used to prepare KASP assays for large sample sizes, facilitating higher throughput use of genetic marker screening tools. [ABSTRACT FROM AUTHOR]

Whitemold (WM) is a major disease in common bean (Phaseolus vulgaris L.), and its complex quantitative genetic control limits the development of WM resistant cultivars. WM2.2, one of the nine meta-QTL with a major effect on WM tolerance, explains up to 35% of the phenotypic variation andwas previously mapped to a large genomic interval on Pv02. Our objective was to narrow the interval of thisQTL using combined approach of classic QTL mapping and QTL-based bulk segregant analysis (BSA), and confirming those results with Khufu de novo QTL-seq. The phenotypic and genotypic data from two RIL populations, 'Raven'/I9365-31 (R31) and 'AN-37'/PS02-029C-20 (Z0726-9), were used to select resistant and susceptible lines to generate subpopulations for bulk DNA sequencing. The QTL physical interval was determined by considering overlapping interval of the identified QTL or peak region in both populations by three independent QTL mapping analyses. Our findings revealed that meta-QTL WM2.2 consists of three regions, WM2.2a (4.27-5.76 Mb; euchromatic), WM 2.2b (12.19 to 17.61 Mb; heterochromatic), and WM2.2c (23.01-25.74 Mb; heterochromatic) found in both populations. Gene models encoding for gibberellin 2-oxidase 8, pentatricopeptide repeat, and heat-shock proteins are the likely candidate genes associated with WM2.2a resistance. A TIR-NBS-LRR class of disease resistance protein (Phvul.002G09200) and LRR domain containing family proteins are potential candidate genes associated with WM2.2b resistance. Nine gene models encoding disease resistance protein [pathogenesis-related thaumatin superfamily protein and disease resistance-responsive (dirigent-like protein) family protein etc] found within theWM2.2c QTL interval are putative candidate genes. WM2.2a region is most likely associated with avoidance mechanisms while WM2.2b and WM2.2c regions trigger physiological resistance based on putative candidate genes. [ABSTRACT FROM AUTHOR]

Beet curly top virus (BCTV), which is synonymous with curly top virus (CTV), causes significant yield loss in common bean (snap and dry beans) cultivars and several other important crops. Common bean cultivars have been found to be resistant to CTV, but screening for resistance is challenging due to the cyclical nature of epidemics and spotty feeding by the leafhopper that vectors the virus. We used an SNP dataset for the Snap Bean Association Panel (SnAP) agroinoculated with CTV-Logan (CA/Logan) strain to locate the Bct gene region to a 1.7-Mb interval on chromosome Pv07 using genome-wide association study (GWAS) analysis. Recombinant lines from the SnAP were used to further narrow the Bct region to a 58.0-kb interval. A missense SNP (S07_2970381) in candidate gene Phvul.007G036300 Exonuclease V (EXO5) was identified as the most likely causal mutation, and it was the most significant SNP detected by GWAS in a dry bean population (DBP) naturally infected by the CTV-Worland (Wor) strain. Tmshift assay markers developed for SNP S07_2970381 and two linked SNPs, S07_2970276 and S07_2966197, were useful for tracking different origins of the Bct EXO5 candidate gene resistance to CTV in common bean. The three SNPs identified four haplotypes, with haplotype 3-1 (Haplo3-1) of Middle American origin associated with the highest levels of CTV resistance. This SNPhaplotype assay will enable breeders to track resistance sources and to develop cultivars with better CTV resistance. [ABSTRACT FROM AUTHOR]

The pinto bean (Phaseolus vulgaris L.), 'USDA Rattler' (Reg. no. CV‐350, PI 693789), was released by the USDA‐ARS in 2021 as a high‐yielding, upright, full‐season cultivar with abiotic stress tolerance. It was bred for broad adaptation to the different bean production regions across the United States by selection for high yield performance under nonstress and multiple stress trials in Washington state. The multiple stress trials included a "purgatory" plot with low fertility, intermittent drought, and soil compaction, and a separate trial which simulated terminal drought. Conversely, the nonstress trials were well watered and fertilized to optimize yield potential. Yield stability is evidenced by the mean seed yield for the breeding line PT11‐13, from which USDA Rattler was selected, numerically exceeding the trial means for 33 of 38 location‐years. Broad adaptation for USDA Rattler is further evidenced by an average seed yield of 4547 kg ha−1 across 10 location‐years in the Cooperative Dry Bean Nursery. Genetic markers as well as pathogen testing indicate USDA Rattler has I and bc‐3 gene combination for durable resistance to all known strains of Bean common mosaic virus and Bean common mosaic necrosis virus. Greenhouse testing with four races of the rust pathogen indicated USDA Rattler is fixed for the Ur‐3 resistance gene but is heterogenous for presence of the Ur‐11 resistance gene. The seed size, appearance, and canning quality characteristics of USDA Rattler meets the industry standards for packaging and processing. Core Ideas: USDA Rattler was bred for high yield potential under both favorable and stressful environments.USDA Rattler performed well in our "purgatory plot" used to select for drought and low soil fertility tolerance.USDA Rattler is resistant to all known strains of Bean common mosaic virus and Bean common mosaic necrosis virus.USDA Rattler is widely adapted to production regions across the United States. [ABSTRACT FROM AUTHOR]

The classic V (violet, purple) gene of common bean (Phaseolus vulgaris) functions in a complex genetic network that controls seed coat and flower color and flavonoid content. V was cloned to understand its role in the network and the evolution of its orthologs in the Viridiplantae. V mapped genetically to a narrow interval on chromosome Pv06. A candidate gene was selected based on flavonoid analysis and confirmed by recombinational mapping. Protein and domain modeling determined V encodes flavonoid 3′5′ hydroxylase (F3′5′H), a P450 enzyme required for the expression of dihydromyricetin-derived flavonoids in the flavonoid pathway. Eight recessive haplotypes, defined by mutations of key functional domains required for P450 activities, evolved independently in the two bean gene pools from a common ancestral gene. V homologs were identified in Viridiplantae orders by functional domain searches. A phylogenetic analysis determined F3′5′H first appeared in the Streptophyta and is present in only 41% of Angiosperm reference genomes. The evolutionarily related flavonoid pathway gene flavonoid 3′ hydroxylase (F3′H) is found nearly universally in all Angiosperms. F3′H may be conserved because of its role in abiotic stress, while F3′5′H evolved as a major target gene for the evolution of flower and seed coat color in plants. [ABSTRACT FROM AUTHOR]

Bean common mosaic virus (BCMV) is a major disease in common bean (Phaseolus vulgaris L.). Host plant resistance is the most effective strategy to minimize crop damage against BCMV and the related Bean common mosaic necrosis virus (BCMNV). To facilitate breeding for resistance, we sought to identify candidate genes and develop markers for the bc-2 gene and the unknown gene with which it interacts. Genome-wide association study (GWAS) of the Durango Diversity Panel (DDP) identified a peak region for bc-2 on chromosome Pv11. Haplotype mapping narrowed the bc-2 genomic interval and identified Phvul.011G092700, a vacuolar protein-sorting 4 (Vps4) AAA+ ATPase endosomal sorting complexes required for transport (ESCRT) protein, as the bc-2 candidate gene. The race Durango Phvul.011G092700 gene model, bc-2 [UI111], contains a 10-kb deletion, while the race Mesoamerican bc-2 [Robust] consists of a single nucleotide polymorphism (SNP) deletion. Each mutation introduces a premature stop codon, and they exhibit the same interaction with the pathogroups (PGs) tested. Phvul.005G125100, another Vps4 AAA+ ATPase ESCRT protein, was identified as the candidate gene for the new recessive bc-4 gene, and the recessive allele is likely an amino acid substitution in the microtubule interacting and transport (MIT) domain. The two Vps4 AAA+ ATPase ESCRT proteins exhibit high similarity to the Zym Cucsa.385040 candidate gene associated with recessive resistance to Zucchini yellow mosaic virus in cucumber. bc-2 alone has no resistance effect but, when combined with bc-4 , provides resistance to BCMV (except PG-V) but not BCMNV, and, when combined with bc-u d, provides resistance to BCMV (except BCMV PG-VII) and BCMNV. So instead of different resistance alleles (i.e., bc-2 and bc-2 2), there is only bc-2 with a differential reaction based on whether it is combined with bc-4 or bc-u d , which are tightly linked in repulsion. The new tools and enhanced understanding of this host-virus pathogen interaction will facilitate breeding common beans for resistance to BCMV and BCMNV. [ABSTRACT FROM AUTHOR]

Bean common mosaic necrosis virus (BCMNV) is a major disease in common bean (Phaseolus vulgaris L.). Host plant resistance is the primary disease control. We sought to identify candidate genes to better understand the host-pathogen interaction and develop tools for marker-assisted selection (MAS). A genome-wide association study (GWAS) approach using 182 lines from a race Durango Diversity Panel (DDP) challenged by BCMNV isolates NL-8 [Pathogroup (PG)-III] and NL-3 (PG-VI), and genotyped with 1.26 million single-nucleotide polymorphisms (SNPs), revealed significant peak regions on chromosomes Pv03 and Pv05, which correspond to bc-1 and bc-u resistance gene loci, respectively. Three candidate genes were identified for NL-3 and NL-8 resistance. Side-by-side receptor-like protein kinases (RLKs), Phvul.003G038700 and Phvul.003G038800 were candidate genes for bc-1. These RLKs were orthologous to linked RLKs associated with virus resistance in soybean (Glycine max). A basic Leucine Zipper (bZIP) transcription factor protein is the candidate gene for bc-u. bZIP protein gene Phvul.005G124100 carries a unique non-synonymous mutation at codon 14 in the first exon (Pv05: 36,114,516 bases), resulting in a premature termination codon that causes a nonfunctional protein. SNP markers for bc-1 and bc-u and new markers for I and bc-3 genes were used to genotype the resistance genes underpinning BCMNV phenotypes in the DDP, host group (HG) differentials, and segregating F3 families. Results revealed major adjustments to the current host-pathogen interaction model: (i) there is only one resistance allele bc-1 for the Bc-1 locus, and differential expression of the allele is based on presence vs. absence of bc-u ; (ii) bc-1 exhibits dominance and incomplete dominance; (iii) bc-1 alone confers resistance to NL-8; (iv) bc-u was absent from HGs 2, 4, 5, and 7 necessitating a new gene symbol bc-u d to reflect this change; (v) bc-u d alone delays susceptible symptoms, and when combined with bc-1 enhanced resistance to NL-3; and (vi) bc-u d is on Pv05, not Pv03 as previously thought. These candidate genes, markers, and adjustments to the host-pathogen interaction will facilitate breeding for resistance to BCMNV and related Bean common mosaic virus (BCMV) in common bean. [ABSTRACT FROM AUTHOR]

Identifying the molecular basis of resistance to pathogens is critical to promote a chemical-free cropping system. In plants, nucleotide-binding leucine-rich repeat constitute the largest family of disease resistance (R) genes, but this resistance can be rapidly overcome by the pathogen, prompting research into alternative sources of resistance. Anthracnose, caused by the fungus Colletotrichum lindemuthianum , is one of the most important diseases of common bean. This study aimed to identify the molecular basis of Co-x , an anthracnose R gene conferring total resistance to the extremely virulent C. lindemuthianum strain 100. To that end, we sequenced the Co-x 58 kb target region in the resistant JaloEEP558 (Co-x) common bean and identified KTR2/3 , an additional gene encoding a truncated and chimeric CRINKLY4 kinase, located within a CRINKLY4 kinase cluster. The presence of KTR2/3 is strictly correlated with resistance to strain 100 in a diversity panel of common beans. Furthermore, KTR2/3 expression is up-regulated 24 hours post-inoculation and its transient expression in a susceptible genotype increases resistance to strain 100. Our results provide evidence that Co-x encodes a truncated and chimeric CRINKLY4 kinase probably resulting from an unequal recombination event that occurred recently in the Andean domesticated gene pool. This atypical R gene may act as a decoy involved in indirect recognition of a fungal effector. [ABSTRACT FROM AUTHOR]

Genetic resistance is the primary means for control of Bean golden yellow mosaic virus (BGYMV) in common bean (Phaseolus vulgaris L.). Breeding for resistance is difficult because of sporadic and uneven infection across field nurseries. We sought to facilitate breeding for BGYMV resistance by improving marker-assisted selection (MAS) for the recessive bgm-1 gene and identifying and developing MAS for quantitative trait loci (QTL) conditioning resistance. Genetic linkage mapping in two recombinant inbred line populations and genome-wide association study (GWAS) in a large breeding population and two diversity panels revealed a candidate gene for bgm-1 and three QTL BGY4.1, BGY7.1, and BGY8.1 on independent chromosomes. A mutation (5 bp deletion) in a NAC (No Apical Meristem) domain transcriptional regulator superfamily protein gene Phvul.003G027100 on chromosome Pv03 corresponded with the recessive bgm-1 resistance allele. The five bp deletion in exon 2 starting at 20 bp (Pv03: 2,601,582) is expected to cause a stop codon at codon 23 (Pv03: 2,601,625), disrupting further translation of the gene. A T m -shift assay marker named PvNAC1 was developed to track bgm-1. PvNAC1 corresponded with bgm-1 across ∼1,000 lines which trace bgm-1 back to a single landrace "Garrapato" from Mexico. BGY8.1 has no effect on its own but exhibited a major effect when combined with bgm-1. BGY4.1 and BGY7.1 acted additively, and they enhanced the level of resistance when combined with bgm-1. T m -shift assay markers were generated for MAS of the QTL, but their effectiveness requires further validation. [ABSTRACT FROM AUTHOR]

Pseudomonas syringae pv. phaseolicola (Psph) Race 6 is a globally prevalent and broadly virulent bacterial pathogen with devastating impact causing halo blight of common bean (Phaseolus vulgaris L.). Common bean lines PI 150414 and CAL 143 are known sources of resistance against this pathogen. We constructed high-resolution linkage maps for three recombinant inbred populations to map resistance to Psph Race 6 derived from the two common bean lines. This was complemented with a genome-wide association study (GWAS) of Race 6 resistance in an Andean Diversity Panel of common bean. Race 6 resistance from PI 150414 maps to a single major-effect quantitative trait locus (QTL; HB4.2) on chromosome Pv04 and confers broad-spectrum resistance to eight other races of the pathogen. Resistance segregating in a Rojo x CAL 143 population maps to five chromosome arms and includes HB4.2. GWAS detected one QTL (HB5.1) on chromosome Pv05 for resistance to Race 6 with significant influence on seed yield. The same HB5.1 QTL, found in both Canadian Wonder x PI 150414 and Rojo x CAL 143 populations, was effective against Race 6 but lacks broad resistance. This study provides evidence for marker-assisted breeding for more durable halo blight control in common bean by combining alleles of race-nonspecific resistance (HB4.2 from PI 150414) and race-specific resistance (HB5.1 from cv. Rojo). [ABSTRACT FROM AUTHOR]

Dry beans (Phaseolus vulgaris L.) of the Andean gene pool, including red mottled, kidney, cranberry, and yellow seed types are important in Africa and the Americas. Andean dry bean breeding gains have lagged behind those of Mesoamerican beans. This difference may result from a narrower genetic base in the Andean gene pool and reduced breeding efforts. The objective of this research was to establish, genotype, and phenotype a panel of bean germplasm to be used for Andean dry bean breeding. An Andean diversity panel (ADP) was assembled, consisting of 396 accessions and including important cultivars, breeding lines, and landraces that originate mostly from Africa, the Caribbean, and North and South America. The panel was genotyped using the Illumina BARCBean6K_3 SNP BeadChip. The population contained two subgroups: Andean and Mesoamerican bean germplasm. The ADP was comprised of 349 Andean, 21 Mesoamerican, and 26 Andean-Mesoamerican admixed accessions. Most admixed lines came from Africa (12 accessions) and the Caribbean (five accessions). Association mapping was conducted for determinacy. Significant single-nucleotide polymorphism (SNP) trait associations were found on chromosome Pv01, with the most significant SNP marker being 3.1 kb from the Terminal Flower 1 PvTFL1y gene. The ADP was evaluated for numerous traits in field trials in the United States and Africa. Variability was found for resistance to rust, angular leaf spot and common bacterial blight diseases; tolerance to low soil fertility; cooking time; and other traits that can be used to improve Andean bean germplasm for Africa and the Americas. [ABSTRACT FROM AUTHOR]

Halo bacterial blight caused by Pseudomonas syringae pv. phaseolicola (Psp) is a serious seed-borne disease of common bean (Phaseolus vulgaris L.). The disease can be controlled by major resistance (R) genes effective against specific races of the pathogen. Our objective was to characterize the R gene(s) conferring resistance to Psp Races 1, 5, 7, and 9 in the great northern dry bean germplasm release BelNeb-RR-1. A recombinant inbred population consisting of 76 F9-derived lines (RILs) from the cross BelNeb-RR-1/A55 was inoculated with Races 1, 5, 7, and 9 and genotyped with 5398 single nucleotide polymorphism markers. Resistance to Races 1, 5, 7, and 9 cosegregated with each other and mapped to the proximal end of Pv04 in a known region of R genes that condition resistance to bean anthracnose and bean rust. Location on Pv04, combined with F2 allelism tests, confirmed the presence of a new gene, Pse-6, for halo blight resistance. We mapped other unnamed R genes to proximal end of Pv04 that were segregating in Minuette/ OSU5630 and Raven/I9365-31 RIL populations and that conditioned resistance to Psp Race 7 and Race 1, respectively. A second R gene, Pse-4, conditioning resistance solely to Race 5, was detected in BelNeb-RR-1 and tentatively positioned on chromosome Pv10. A sequencecharacterized amplified region marker SB10.550 tightly linked (1.4 cM) with Pse-6 was generated for potential use in marker-assisted selection for resistance to halo bacterial blight. [ABSTRACT FROM AUTHOR]

Common bacterial blight is a severe disease of common bean (Phaseolus vulgaris L.) worldwide. Use of resistant cultivars is crucial for its control. The objectives were to (i) assess the progress made in breeding large-seeded Andean bean developed between 1974 and 2010 and (ii) determine their resistance-linked sequence characterized amplified region (SCAR) marker composition. Ten Andean and four Middle American common bacterial blight resistant beans including checks were evaluated in the greenhouse in 2011. Bacterial strains ARX8AC and Xcp25 were used to inoculate primary and trifoliolate leaves. The mean disease score of the trifoliolate was 5.0 and of the primary leaf was 2.8. Strain Xcp25 had a mean score of 3.8 in primary and 5.9 in trifoliolate leaves. The respective scores for ARX8AC were 1.9 and 4.2. Andean 'Montcalm', with the SAP6 quantitative trait loci (QTL) and USDK-CBB-15, and USWK-CBB-17, with the SAP6 and SU91 QTL, showed an intermediate response to ARX8AC and a susceptible response to Xcp25. Middle American VAX 1 with SAP6, Andeans 08SH-840 and CXR 1 with SAP6 and SU91, and RCS52-2, RCS53-3, and RCS63-5B with SU91 and BC420 were resistant or intermediate to both strains. Middle American VAX 3 and VAX 6, with SAP6 and SU91, had the highest levels of resistance to ARX8AC, but their responses to Xcp25 were similar to the latter Andean group. Thus, significant improvement has been achieved, but breeding for yet higher levels of resistance, recovery of commercial seed types, and improving yield and other agronomic traits should be emphasized. [ABSTRACT FROM AUTHOR]

White mold caused by the necrotrophic fungus Sclerotinia sclerotiorum (Lib.) de Bary limits common bean (Phaseolus vulgaris L.) production in temperate climates. Disease resistance has been identified, but breeding is hampered by a paucity of resistance sources and complex inheritance, as numerous quantitative trait loci (QTL) conditioning partial resistance have been found. Our objectives were to characterize the partial white mold resistance found in breeding lines 19365-31 and VA19 and to construct a comparative linkage map for all the white mold resistance QTL identified to date. Recombinant inbred line (RIL) populations `Benton'/VA19 (BV) and `Raven'/l9365-31 (R31) consisting of 79 F5 and 105 F5 RILs, respectively, were evaluated for white mold (WM) reaction in multiple green-house and field tests. Two QTL were found in By, WM2.2 expressed in the greenhouse (R² = 33%) and the field (13%) and WM8.3 expressed in field (11%) only, and seven were found in R31 (WM2.2, WM4.2, WM5.3, WM5.4, WM6.1, WM7.3, WM8.4), three expressed in greenhouse tests and four in the field, ranging in phenotypic variance from 5 to 52%. These QTL were compared with 26 previously identified QTL, resulting in a comparative linkage map of 35 QTL, which coalesced into 21 distinct regions across nine linkage groups. Four QTL found in R31 were novel. Sequence characterized amplified region markers associated with WM2.2, WM8.3, and WM7.3 QTL were generated. The comparative linkage map provides a framework for integrating and interpreting future QTL studies concerning white mold resistance in common bean. [ABSTRACT FROM AUTHOR]

Genetic resistance is an important component of integrated strategies used to control problematic diseases in common bean (Phaseolus vulgaris L.). Molecular linkage maps have been used to identify, tag, and map disease resistance genes and QTL in common bean, leading to improved breeding strategies and implementation of marker-assisted selection. Most widely used marker types, random amplified polymorphic DNA (RAPD) and amplified fragment length polymorphisms (AFLP), for linkage mapping in bean are located randomly throughout the genuine and associate with particular traits by chance. We sought to determine the potential application of a new marker system, TRAP, which uses expressed sequence information and a bioinformatics approach to generate polymorphic markers around targeted candidate gene sequences. TRAP markers were amplified by fixed primers designed against sequenced expressed sequence tag (EST) associated with disease resistance in the Compositae Genomics database or against sequenced resistance gene analog (RGA) from common bean. Seventeen of 85 TRAP markers located in the BAT 93/Jalo EEP558 core mapping population mapped in the vicinity of R genes. Six of 21 TRAP markers generated in the Dorado/XAN 176 mapping population were linked with newly identified QTL, two conditioning resistance to ashy stem blight (14% and 16% of the phenotypic variation explained, R²), and one each conferring resistance to Bean golden yellow mosaic virus (BGYMV) (15%) and common bacterial blight (30%). The TRAP marker system has potential for mapping regions of the common bean genome linked with disease resistance. [ABSTRACT FROM AUTHOR]

Resistance (R) genes containing nucleotide-binding site (NBS)-leucine rich repeats (LRR) are the most prevalent types of R gene in plants. The objective of this study was to develop PCR-based R-gene analog polymorphism (RGAP) markers for common bean ( Phaseolus vulgaris L). Twenty degenerate primers were designed from the conserved kinase-1a (GVGKTT) and hydrophobic domains (GLPLAL) of known NBS-LRR type R-genes and from EST databases. Sixty-six of the 100 primer combinations tested yielded polymorphism. Thirty-two RGAP markers were mapped in the BAT 93/Jalo EEP558 core mapping population for common bean. The markers mapped to 10 of 11 linkage groups with a strong tendency for clustering. In addition, the RGAP markers co-located, on six linkage groups, with 15 resistance gene analogs (RGAs) that were previously mapped in other populations of common bean. The distance between the priming sites in NBS-LRR type R-genes is around 500 bp. Of the 32 RGAP markers, 19 had sizes larger and 13 less than 500 bp. RGAP markers mapped close to known R-genes on B11, and to QTLs for resistance on B1, B2, B6, B7, B8, B10, and B11. RGAP appears to provide a useful marker technique for tagging and mapping R-genes in segregating common bean populations, discovery of candidate genes underlying resistance QTL, and future cloning of R-genes in common bean. [ABSTRACT FROM AUTHOR]

Pinto beans (Phaseolus vulgaris L.) of cool subtropical and temperate origins are extremely susceptible to white mold disease caused by Sclerotinia sclerotiorum (Lib.) de Bary. Breeding pinto beans with resistance to white mold is difficult because of the paucity of resistant germplasm in a closely related background. White mold resistant 'ICA Bunsi', a small white navy bean, is from the same Middle American gene pool, but it is of warm tropical origin and needs to be exploited in pinto bean improvement. Our objectives were to determine inheritance of ICA Bunsi-derived resistance in a cross with pinto bean, determine association of the resistance with disease avoidance, and identify white mold resistant pinto beans. White mold reactions of 85 F5:8 recombinant inbred lines (RIL) from the cross 'Aztec'/ND88- 106-04 were characterized in the field in North Dakota and Washington in 2001 and 2002. Aztec pinto is susceptible to white mold, and ND88-106-04 navy bean has partial resistance derived from ICA Bunsi. Disease severity score (1 = no disease to 9 = completely susceptible), yield, and disease avoidance traits were measured. Disease severity for Aztec and ND88-106-04 across environments was 6.9 and 2.5, respectively, compared with 4.6 for WA Bunsi. Reduced lodging and late maturity enhanced disease avoidance. The RILs with stay-green stem at harvest, similar to ND88-106-04, also exhibited less disease. Normal distribution and moderate heritability (Hns = 56 and 36% for WA and ND environments, respectively) for disease score indicated resistance was influenced by environment and likely conditioned by genes with small effects. Nonetheless, white mold resistance was present in a few RILs with high yield potential and pinto seed type. [ABSTRACT FROM AUTHOR]

Copyright of Genome is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The genetic improvement of economically important production traits of dry bean (Phaseolus vulgaris L.), for geographic regions where production is threatened by drought and high temperature stress, is challenging because of the complex genetic nature of these traits. Large scale SNP data sets for the two major gene pools of bean, Andean and Middle American, were developed by mapping multiple pools of genotype-bysequencing reads and identifying over 200k SNPs for each gene pool against the most recent assembly of the P. vulgaris genome sequence. Moderately sized Bean Abiotic Stress Evaluation (BASE) panels, consisting of genotypes appropriate for production in Central America and Africa, were assembled. Phylogenetic analyses demonstrated the BASE populations represented broad genetic diversity for the appropriate races within the two gene pools. Joint mixed linear model genome-wide association studies with data from multiple locations discovered genetic factors associated with four production traits in both heat and drought stress environments using the BASE panels. Pleiotropic genetic factors were discovered using a multi-trait mixed model analysis. SNPs within or near candidate genes associated with hormone signaling, epigenetic regulation, and ROS detoxification under stress conditions were identified and can be used as genetic markers in dry bean breeding programs. [ABSTRACT FROM AUTHOR]

• Seedling root architecture is related to yield in some environments. • Gene pools and races vary significantly for root architecture. • Integrated root phenotypes are related to yield in some environments. • Seedling root architectural phenes are a valuable breeding targets. Seedling root phenotypes may have important impacts on fitness and are more easily measured than mature root phenotypes. We phenotyped the roots of 577 genotypes of common bean (Phaseolus vulgaris), representing the bulk of the genetic diversity for recent cultivars and landraces in this species. Root architectural phenotypes of seedlings germinated for nine days were compared to root architectural phenotypes in the field as well as seed yield across 51 environments with an array of abiotic stresses including drought, nutrient deficiency, and heat, as well as non-stress conditions. We observed repeatability ranging from 0.52–0.57 for measures of root phenotypes in seedlings, significant variation in root phene states between gene pools and races, relationships between seedling and field phenotypes, and varying correlations between seedling root phenes and seed yield under a variety of environmental conditions. Seed yield was significantly related to seedling basal root number in 22% of environments, seedling adventitious root abundance in 35% of environments, and seedling taproot length in 12% of environments. Cluster analysis grouped genotypes by their aggregated seedling root phenotype, and variation in seed yield among these clusters under non-stress, drought, and low fertility conditions was observed. These results highlight the existence and influence of integrated root phenotypes for adaptation to edaphic stress, and suggest root phenes have value as breeding targets under real-world conditions. [ABSTRACT FROM AUTHOR]