ABSTRACT
Abstract Bacterial leaf blight (BLB) is one of the major rice diseases in Malaysia. This disease causes substantial yield loss as high as 70%. Development of rice varieties which inherited BLB resistant traits is a crucial approach to promote and sustain rice industry in Malaysia. Hence, this study aims were to enhance BLB disease resistant characters of high yielding commercial variety MR219 through backcross breeding approach with supporting tool of marker-assisted selection (MAS). Broad spectrum BLB resistance gene, Xa7 from donor parent IRBB7 were introgressed into the susceptible MR219 (recurrent parent) using two flanking markers ID7 and ID15. At BC3F4, we managed to generate 19 introgressed lines with homozygous Xa7 gene and showed resistant characteristics as donor parent when it was challenged with Xanthomonas oryzae pv. oryzae through artificial inoculation. Recurrent parent MR219 and control variety, MR263 were found to be severely infected by the disease. The improved lines exhibited similar morphological and yield performance characters as to the elite variety, MR219. Two lines, PB-2-107 and PB-2-34 were chosen to be potential lines because of their outstanding performances compared to parent, MR219. This study demonstrates a success story of MAS application in development of improved disease resistance lines of rice against BLB disease.
Resumo A mancha bacteriana das folhas (BLB) é uma das principais doenças do arroz na Malásia. Essa doença causa perdas substanciais de rendimento de até 70%. O desenvolvimento de variedades de arroz que herdaram características de resistência ao BLB é uma abordagem crucial para promover e sustentar a indústria do arroz na Malásia. Portanto, o objetivo deste estudo foi aumentar os caracteres BLB resistentes a doenças da variedade comercial MR219 de alto rendimento por meio de uma abordagem de cruzamento retrocruzamento com ferramenta de apoio de seleção assistida por marcador (MAS). O gene de resistência a BLB de amplo espectro, Xa7 do pai doador IRBB7, foi introgressado no MR219 suscetível (pai recorrente) usando dois marcadores flanqueadores ID7 e ID15. No BC3F4, conseguimos gerar 19 linhagens introgressadas com o gene Xa7 homozigoto e apresentamos características de resistência como genitor doador quando desafiado com Xanthomonas oryzae pv. oryzae por inoculação artificial. O pai recorrente MR219 e a variedade controle, MR263, estavam gravemente infectados pela doença. As linhas melhoradas exibiram características morfológicas e de desempenho de rendimento semelhantes às da variedade elite, MR219. Duas linhas, PB-2-107 e PB-2-34, foram escolhidas como linhas potenciais por causa de seus desempenhos excelentes em comparação com a mãe, MR219. Este estudo demonstra uma história de sucesso de aplicação de MAS no desenvolvimento de linhas de arroz melhoradas com resistência a doenças contra a doença BLB.
ABSTRACT
Abstract Bacterial leaf blight (BLB) is one of the major rice diseases in Malaysia. This disease causes substantial yield loss as high as 70%. Development of rice varieties which inherited BLB resistant traits is a crucial approach to promote and sustain rice industry in Malaysia. Hence, this study aims were to enhance BLB disease resistant characters of high yielding commercial variety MR219 through backcross breeding approach with supporting tool of marker-assisted selection (MAS). Broad spectrum BLB resistance gene, Xa7 from donor parent IRBB7 were introgressed into the susceptible MR219 (recurrent parent) using two flanking markers ID7 and ID15. At BC3F4, we managed to generate 19 introgressed lines with homozygous Xa7 gene and showed resistant characteristics as donor parent when it was challenged with Xanthomonas oryzae pv. oryzae through artificial inoculation. Recurrent parent MR219 and control variety, MR263 were found to be severely infected by the disease. The improved lines exhibited similar morphological and yield performance characters as to the elite variety, MR219. Two lines, PB-2-107 and PB-2-34 were chosen to be potential lines because of their outstanding performances compared to parent, MR219. This study demonstrates a success story of MAS application in development of improved disease resistance lines of rice against BLB disease.
Resumo A mancha bacteriana das folhas (BLB) é uma das principais doenças do arroz na Malásia. Essa doença causa perdas substanciais de rendimento de até 70%. O desenvolvimento de variedades de arroz que herdaram características de resistência ao BLB é uma abordagem crucial para promover e sustentar a indústria do arroz na Malásia. Portanto, o objetivo deste estudo foi aumentar os caracteres BLB resistentes a doenças da variedade comercial MR219 de alto rendimento por meio de uma abordagem de cruzamento retrocruzamento com ferramenta de apoio de seleção assistida por marcador (MAS). O gene de resistência a BLB de amplo espectro, Xa7 do pai doador IRBB7, foi introgressado no MR219 suscetível (pai recorrente) usando dois marcadores flanqueadores ID7 e ID15. No BC3F4, conseguimos gerar 19 linhagens introgressadas com o gene Xa7 homozigoto e apresentamos características de resistência como genitor doador quando desafiado com Xanthomonas oryzae pv. oryzae por inoculação artificial. O pai recorrente MR219 e a variedade controle, MR263, estavam gravemente infectados pela doença. As linhas melhoradas exibiram características morfológicas e de desempenho de rendimento semelhantes às da variedade elite, MR219. Duas linhas, PB-2-107 e PB-2-34, foram escolhidas como linhas potenciais por causa de seus desempenhos excelentes em comparação com a mãe, MR219. Este estudo demonstra uma história de sucesso de aplicação de MAS no desenvolvimento de linhas de arroz melhoradas com resistência a doenças contra a doença BLB.
Subject(s)
Oryza , Xanthomonas , Plant Diseases/genetics , Disease Resistance/genetics , Plant BreedingABSTRACT
ABSTRACT One of the greatest challenges facing humanity is the development of sustainable strategies to ensure food availability in response to population growth and climate change. One approach that can contribute to increase food security is to close yield gaps and enhancing genetic gain; to such end, what is known as "molecular breeding" plays a fundamental role. Since a crop breeding program is mainly based on the quality of the germplasm, its detailed genetic characterization is mandatory to ensure the efficient use of genetic resources and accelerating development of superior varieties. Deep genotyping is an essential tool for a comprehensive characterization of the germplasm of interest and, fortunately, the technology is now accessible at a reasonable cost. What must be ensured is the correct interpretation of the genotypic information and on that basis develop efficient practical molecular crop breeding strategies that respond to the real needs of the breeding program.
RESUMEN Uno de los mayores desafíos que enfrenta la humanidad es el desarrollo de estrategias sostenibles para asegurar la disponibilidad de alimentos en respuesta al crecimiento de la población y el cambio climático. Un enfoque que puede contribuir a aumentar la seguridad alimentaria es cerrar las brechas de rendimiento y mejorar la ganancia genética; para tal fin, lo que se conoce como "mejoramiento molecular" juega un papel fundamental. Dado que un programa de mejoramiento de cultivos se basa principalmente en la calidad del germoplasma, su caracterización genética detallada es fundamental para garantizar el uso eficiente de los recursos genéticos y acelerar el desarrollo de variedades superiores. La genotipificación profunda es una herramienta esencial para una caracterización integral del germoplasma de interés y, afortunadamente, en la actualidad se puede acceder a la tecnología a un costo razonable. Lo que debe asegurarse es la interpretación correcta de la información genotípica y sobre esa base desarrollar estrategias eficientes y prácticas de mejoramiento molecular de cultivos que respondan a las necesidades reales del programa de mejoramiento.
ABSTRACT
BACKGROUND: Wheat is one of the most important crops cultivated all over the world. New high-yielding cultivars that are more resistant to fungal diseases have been permanently developed. The present study aimed at the possibility of accelerating the process of breeding new cultivars, resistant to eyespot, by using doubled haploids (DH) system supported by marker-assisted selection. RESULTS: Two highly resistant breeding lines (KBP 0916 and KBH 4942/05) carrying Pch1 gene were crossed with the elite wheat genotypes. Hybrid plants of early generations were analyzed using endopeptidase EpD1 and two SSR markers linked to the Pch1 locus. Selected homozygous and heterozygous genotypes for the Pch1-linked EpD1b allele were used to produce haploid plants. Molecular analyses were performed on haploids to identify plants possessing Pch1 gene. Chromosome doubling was performed only on haploid plants with Pch1 gene. Finally, 65 DH lines carrying eyespot resistance gene Pch1 and 30 lines without this gene were chosen for the eyespot resistance phenotyping in a field experiment. CONCLUSIONS: Results of the experiment confirmed higher resistance to eyespot of the genotypes with Pch1 in comparison to those without this gene. This indicates the efficiency of selection at the haploid level.
Subject(s)
Selection, Genetic , Triticum/genetics , Triticum/metabolism , Haploidy , Plant Diseases , Breeding/methods , Gene Expression , Microsatellite Repeats , GenotypeABSTRACT
Abstract Background: Tilapia is the most farmed fish in Colombia. However, the genetic diversity and structure of broodstocks in the hatcheries of Antioquia province remains unknown. Objective: To analyze the genetic diversity and structure of one Nile and three red tilapia broodstocks in Antioquia, Colombia. Methods: Fish were genotyped using 24 microsatellite markers of 13 linkage groups in five multiple reactions. Genetic diversity metrics were estimated and null alleles were detected. Analysis of Molecular Variance and analysis of number of clusters were used to describe the relationship between broodstocks. Results: Two microsatellites could not be amplified, and 22 were polymorphic. Average number of alleles per locus ranged 5.77 to 7.91. Locus UNH211 had the most alleles (17), whereas OMO032 had the fewest (4). Except for GM234 and OMO032, the analyzed loci had at least one private allele per population. Average effective number of alleles (3.37-4.03) was always less than the number of observed alleles. Significant deviations from Hardy-Weinberg equilibrium with heterozygote deficiencies were registered. Nine markers showed evidence of null alleles. The expected heterozygosity (0.65 to 0.67 per broodstock) was significantly higher than the observed heterozygosity (0.601 to 0.649) in the four populations. The fixation index for all broodstocks (excluding null alleles) was 0.0766 (95% confidence interval, 0.05092 to 0.10289). According to the molecular variance analysis, the greatest variation was between individuals rather than between groups of broodstocks or individuals within broodstocks. The genetic distance between the Nile and red broodstocks ranged from 0.43 to 0.54. Conclusions: Overall, these findings provide baseline information about the genetic diversity and structure of tilapia broodstocks in Antioquia, Colombia, useful for the management of hatcheries.
Resumen Antecedentes: La tilapia es el pez más cultivado en Colombia; sin embargo, hay gran desconocimiento sobre la estructura genetica actual de los reproductores. Objetivo: Analizar la diversidad y estructura genética de los reproductores de tres granjas de tilapia roja y una de tilapia Nilótica en Antioquia, Colombia. Métodos: Se utilizaron 24 microsatélites de 13 grupos de ligamiento amplificados en cinco reacciones múltiples. Se calcularon diferentes medidas de diversidad y se detectaron alelos nulos. Se utilizó un análisis de varianza molecular y uno de número de grupos para describir las relaciones entre las granjas de reproductores. Resultados: Dos marcadores no fueron amplificados y los 22 restantes fueron polimórficos. El promedio de alelos por locus varió entre 5,77 y 7,91. El mayor número de alelos (17) se encontró en el locus UNH 211, mientras que el menor se observó en OMO032 (cuatro). Veinte loci presentaron por lo menos un alelo privado. El número de alelos efectivos promedio fue menor al número de alelos observado y estuvo entre 3,37 y 4,03. Se registraron desviaciones significativas en el equilibrio Hardy-Weinberg, en su mayoría con deficiencias de heterocigotos. Se encontraron evidencias de alelos nulos en nueve marcadores. La heterocigosidad observada estuvo entre 0,601 y 0,649. El índice de fijación fue de 0.0766 (intervalo de confianza de 95%, entre 0,05092 y 0,10289). Según el análisis de varianza molecular, la mayor fuente de variación se encontró entre individuos. El valor de la distancia de Nei entre los reproductores Nilóticos y rojos estuvo entre 0,43 y 0,54. Conclusión: Los resultados de la presente investigación proveen una línea base acerca de la diversidad y estructura genética de los reproductores de tilapia en Antioquia, Colombia, y son útiles para el manejo de granjas dedicadas a la reproducción de tilapia.
Resumo Antecedentes: A tilápia é o peixe mais cultivado na Colômbia. É importante examinar a diversidade genética de peixes reprodutores. Objetivo: Avaliar a diversidade e estrutura genética de três estoques de reprodutores de tilápias vermelhas e um de tilápia Nilótica em Antioquia, Colômbia. Métodos: Utilizaram-se 24 microssatélites de 13 grupos de ligação em cinco reações múltiplas. Métricas de diversidade genética foram estimadas e alelos nulos foram detectados. Análise da Variância Molecular e análise do número de clusters foram utilizados para descrever a relação entre os estoques. Resultados: Dois marcadores não foram amplificados e vinte e dois microssatélites analisados mostraram-se polimórficos. O número médio de alelos por locus variou entre 5,77 e 7,91. O Locus UNH211 apresentou o maior número de alelos (17), enquanto o OMO032 apresentou o menor número (4). Exceto GM234 e OMO032, os loci analisados mostrou um pelo menos um alelo privado por população. O número efetivo médio de alelos (3,37-4,03) foi sempre menor do que o número de alelos observados. Foram observados desvios significativos do equilíbrio Hardy-Weinberg e deficiência de heterozigotos. Nove loci mostraram evidências de alelos nulos. A heterozigosidade esperada (0,6504-0,6748 por população) foi significativamente maior do que a heterozigosidade observada (0,601-0,649). O índice de fixação foi de 0,0766 (intervalo de confiança de 95%, 0,05092-0,10289). De acordo com a análise da variância molecular, a maior variação foi entre indivíduos. Adistância genética entre o Nilo e os reprodutores vermelhos variou de 0,43 a 0,54. Conclusão: No geral, esses resultados fornecem informação básica sobre sobre diversidade e estrutura genética de reprodutores de tilápia em Antioquia, Colômbia, e são significativos para o manejo de plantéis de reprodutores.
ABSTRACT
To improve the blast resistance of elite rice restorer line Fuhui 673, 3 blast resistance genes Pi-1, Pi-9 and Pi-kh were introduced into Fuhui 673 from a good-quality restorer line Jinhui 1059 through 3 successive backcrosses followed by one selfing using the technique of marker-assisted selection. Ten near-isogenic lines (NILs) of Fuhui 673 carrying the 3 introduced resistance genes were created. Genotype analysis using 68 SSR markers evenly distributed in the genome indicated that 92.96%-98.59% of the NILs' genetic background had been recovered to Fuhui 673. Both indoor and field resistance tests indicated that the NILs and their hybrids with sterile line Yixiang A were all resistant to rice blast, with resistance levels significantly higher than those of controls Fuhui 673 and hybrid Yiyou 673 (Yixiang A Fuhui 673). In addition, among the 10 hybrids between the NILs and Yixiang A, 2 showed significantly higher yield than and 4 displayed similar yield to that of control Yiyou 673, suggesting that most of the NILs retained the elite characteristics of Fuhui 673. Two new hybrid rice cultivars Liangyou 7283 and Jintaiyou 683 from NIL Line 9 showed high yield, good resistance to blast and moderate growth period in regional trial, suggesting that the NIL Line 9 has a good prospect for application.
Subject(s)
Breeding , Disease Resistance , Genetics , Genes, Plant , Genetics , Oryza , GeneticsABSTRACT
Yuhua91 is a new peanut variety with high oleic acid content bred by Qingdao Agricultural University. The crossing was conducted with Luhua11 as female parent and with Kainong1715, an F435-type variety with high oleic acid content as male parent. The real F1 hybrids were screened by sequencing on PCR amplification products, and those homozygotes with bb genotype in F2 populations were screened by the same sequencing method as above. The content of oleic and linoleic acid was measured on the kernels harvested from F2 single plants by near infrared ray method, and those kernels whose content of oleic was above 80%, oleic and linoleic acid ratio was above 10.0 were obtained and planted into a row, with pedigree method for subsequent selection breeding. Yuhua91 has some characters of small pod, light and obvious pod texture, 148.06 g per 100 pods, 63.31 g per 100 kernels, 75.15% shelling percentage, long elliptic seed kernel, pink seed coat, without crack, white endotesta. Its content of protein, oil, oleic acid, linoleic acid and palmitic acid was 26.57%, 52.72%, 80.40%, 2.50% and 5.57% respectively. Yuhua91 has other characters of strong seedlings, compact pod areas, and moderate resistance to leaf spot disease and bacterial wilt. Average pod yield is 215.79 kg per Mu, 15.27% higher than the control variety Huayu20. Average seed kernels yield is 157.33 kg per Mu, 21.64% higher than the control variety Huayu20. Yuhua 91 has been registered on department of agriculture in 2018, and the registration No. is GPD peanut (2018) 370210, fit for growing in Shandong Province.
Subject(s)
Arachis , Oleic Acid , Plant Breeding , SeedsABSTRACT
ABSTRACT: Soil salinity limits agricultural production and is a major obstacle for increasing crop yield. Common wheat is one of the most important crops with allohexaploid characteristic and a highly complex genome. QTL mapping is a useful way to identify genes for quantitative traits such as salinity tolerance in hexaploid wheat. In the present study, a hydroponic trial was carried out to identify quantitative trait loci (QTLs) associated with salinity tolerance of wheat under 150mM NaCl concentration using a recombinant inbred line population (Xiaoyan 54×Jing 411). Values of wheat seedling traits including maximum root length (MRL), root dry weight (RDW), shoot dry weight (SDW), total dry weight (TDW) and the ratio of TDW of wheat plants between salt stress and control (TDWR) were evaluated or calculated. A total of 19QTLs for five traits were detected through composite interval mapping method by using QTL Cartographer version 2.5 under normal and salt stress conditions. These QTLs distributed on 12 chromosomes explained the percentage of phenotypic variation by individual QTL varying from 7.9% to 19.0%. Among them, 11 and six QTLs were detected under normal and salt stress conditions, respectively and two QTLs were detected for TDWR. Some salt tolerance related loci may be pleiotropic. Chromosome 1A, 3A and 7A may harbor crucial candidate genes associated with wheat salt tolerance. Our results would be helpful for the marker assisted selection to breed wheat varieties with improved salt tolerance.
RESUMO: A salinidade do solo limita a produção agrícola. O trigo mole é uma das culturas mais importantes com característica allohexaploid e genoma altamente complexo. O mapeamento QTL é uma maneira muito útil de identificar genes para traços quantitativos, como a tolerância à salinidade em trigo hexaplóide. No presente estudo realizou-se um ensaio hidropónico para identificar locos de traços quantitativos (QTLs) associados à tolerância à salinidade do trigo sob concentração de NaCl 150 mM, usando uma população de linhagem consanguíneo recombinante (Xiaoyan 54 × Jing 411). Os valores dos traços de mudas de trigo, incluindo comprimento máximo da raiz (MRL), peso seco da raiz (RDW), ponha o peso seco (SDW), peso seco total (TDW) e a proporção das plantas de trigo TDW entre o estresse salgado e o controle (TDWR), foram avaliados ou calculados. Um total de 19QTLs para cinco traços foram detectados através do método de mapeamento de intervalo composto usando a versão 2.5 do cartógrafo QTL sob condições normais e de estresse salino. Estes QTLs distribuídos em 12 cromossomos explicaram a porcentagem de variação fenotípica por QTL individual variando de 7,9% a 19,0%. Entre eles, foram detectados 11 e 6 QTLs em condições de estresse normal e sal, respectivamente, e dois QTLs foram detectados para TDWR. Cromossoma 1A, 3A e 7A podem conter genes que são candidatos cruciais associados à tolerância ao sal de trigo. Nossos resultados seriam úteis para a seleção assistida por marcadores para produzir variedades de trigo com tolerância salina melhorada.
ABSTRACT
ABSTRACT: Stripe rust, caused by Puccinia striiformis is one of the most destructive diseases of wheat worldwide. CH5389 is a wheat-Thinopyrum intermedium derived line conferring stripe rust resistance. Genetic analyses of seedlings of F2 populations and F2:3 families developed by crossing CH5389 and susceptible common wheat revealed that stripe rust resistance in CH5389 was controlled by a single dominant gene that was designated YrCH5389. Eight SSR and EST-PCR polymorphic markers on chromosome 3AL were identified in F2 population of CH5389/Taichung29. The YrCH5389 was flanked by EST marker BE405348 and SSR marker Xwmc388 on chromosome 3AL with genetic distances of 2.2 and 4.6 cM, respectively. Comparative genomic analysis demonstrated that the orthologous genomic region of YrCH5389 covered 990 kb in rice, 640 kb in Brachypodium, and 890 kb in sorghum. Based on the locations of the markers, the resistance gene was located to chromosome deletion bin 3AL-0.85-1.00. Because there are no officially named stripe rust resistance genes on the 3AL chromosome, the YrCH5389 should be designated as a new resistance gene. These linkage markers could be useful for marker-assisted selection in wheat resistance breeding.
RESUMO: A ferrugem linear causada por Puccinia striiformis é uma das doenças mais destrutivas do trigo no mundo. A linhagem CH5389 é derivada do cruzamento de trigo com Thinopyrum intermedium e confere resistência a ferrugem linear. Análises genéticas de indivíduos da população F2 e família F2:3 obtida a partir do cruzamento entre CH5389 e trigo comum suscetível revelaram que a resistência à ferrugem linear na linhagem CH5389 foi controlada por um único gene dominante, designado YrCH5389. Oito marcadores polimórficos SSR e EST-PCR no cromossomo 3AL foram identificados na população F2 de CH5389/Taichung29. O gene YrCH5389 foi delimitado pelos marcadores EST BE405348 e SSR Xwmc388 no cromossomo 3AL com distâncias genéticas de 2,2 e 4,6 cM, respectivamente. Análises genômicas comparativas demonstraram que regiões genômicas ortólogas do gene YrCH5389 compreendem 990 kb em arroz, 640 kb em braquipódio e 890 kb em sorgo. Com base nas localizações dos marcadores, o gene de resistência foi localizado no cromossomo 3AL-0.85-1.00. Como não há genes oficialmente nomeados de resistência à ferrugem linear no cromossomo 3AL, o YrCH5389 deve ser designado como um gene novo de resistência. Esses marcadores de ligação podem ser úteis para a seleção assistida de genótipos de trigo resistentes a ferrugem linear.
ABSTRACT
ABSTRACT Mungbean (Vigna radiata (L.) Wilczek) also known as green gram is an important source of protein in the category of food legumes. In the present study, SSR marker is used to analyze the genetic diversity amongst 23 genotypes of mungbean. Out of a total of 10 primers used for SSR analysis revealed generation of 15 alleles. The number of alleles per locus ranged from one (CEDG006, CEDG010, CEDG050, CEDG088, CEDG092 and CEDG232) to three (CEDG 214), with an average of 1.5 allele per primer. The index for expected heterozygosity was 0.29 ranging from 0.15 to 0.49 revealed a deficit in heterozygosity. The size of amplification products varied in case of each primer and the range was found to be 100 bp to 190 bp. 13 out of 15 alleles were found polymorphic. The average PIC value of SSR marker was found to be 0.205. The value of Jaccard's similarity coefficient had ranged from 0.28-1.00 with an average value of 0.64. The dendrogram constructed on SSR molecular marker data through UPGMA method and PCA using average linkage, had enabled grouping of the genotypes into three main clusters. Clustering pattern based on SSR marker data clearly indicated the narrow genetic base of mungbean genotypes that emphasizes the need to explore and exploit more number of germplasm from additional source to study genetic variation in mungbean for genetic improvement. The results indicated the marked usefulness of SSR in the assessment of genetic diversity in mungbean crop.
ABSTRACT
Background: Cultivated peanut (Arachis hypogaea L.) is a major oilseed crop worldwide. Fatty acid composition of peanut oil may affect the flavor and shelf life of the resulting food products. Oleic acid and linoleic acid are the major fatty acids of peanut oil. The conversion from oleic acid to linoleic acid is controlled by theΔ12 fatty acid desaturase (FAD) encoded byAhFAD2AandAhFAD2B, two homoeologous genes from A and B subgenomes, respectively. One nucleotide substitution (G:CâA:T) ofAhFAD2Aand an "A" insertion ofAhFAD2Bresulted in high-oleic acid phenotype. Detection ofAhFAD2mutation had been achieved by cleaved amplified polymorphic sequence (CAPS), real-time polymerase chain reaction (qRT-PCR) and allele-specific PCR (AS-PCR). However, a low cost, high throughput and high specific method is still required to detectAhFAD2genotype of large number of seeds. Kompetitive allele specific PCR (KASP) can detect both alleles in a single reaction. The aim of this work is to develop KASP for detectionAhFAD2genotype of large number of breeding materials. Results: Here, we developed a KASP method to detect the genotypes of progenies between high oleic acid peanut and common peanut. Validation was carried out by CAPS analysis. The results from KASP assay and CAPS analysis were consistent. The genotype of 18 out of 179 BC4F2seeds was aabb. Conclusions: Due to high accuracy, time saving, high throughput feature and low cost, KASP is more suitable fordeterminingAhFAD2genotype than other methods.
Subject(s)
Arachis/genetics , High-Throughput Nucleotide Sequencing , Genetic Markers , Polymerase Chain Reaction/methods , Oleic Acid , Fatty Acid Desaturases/genetics , Peanut Oil , Genotype , MutationABSTRACT
DNA marker-assisted selection of medicinal plants is based on the DNA polymorphism, selects the DNA sequences related to the phenotypes such as high yields, superior quality, stress-resistance and so on according to the technologies of molecular hybridization, polymerase chain reaction and high-throughput sequencing, and assists the breeding of new cultivars. This study bred the first disease-resistant cultivar of notoginseng "Miaoxiang Kangqi 1" using the technology of DNA marker-assisted selection of medicinal plants and systematic breeding. The disease-resistant cultivar of notoginseng contained 12 special SNPs based on the analysis of Restriction-site Associated DNA Sequencing (RAD-Seq). Among the SNP (record_519688) was related to the root rot-resistant characteristics, which indicated this SNP could serve as genetic markers of disease-resistant cultivars and assist the systematic breeding. Compared to the conventional cultivated cultivars, the incidence rate of root-rot and rust-rot in notoginseng seedlings decreased by 83.6% and 71.8%, respectively. The incidence rate of root-rot respectively declined by 43.6% and 62.9% in notoginseng cultivation for 2 and 3 years compared with those of the conventional cultivated cultivars. Additionally, the potential disease-resistant groups were screened based on the relative SNP, and this model enlarged the target groups and advanced the breeding efficiency. DNA marker-assisted selection of medicinal plants accelerated the breeding and promotion of new cultivars, and guaranteed the healthy development of Chinese medicinal materials industry.
ABSTRACT
Over the last 20 years, the two uniparentally inherited marker systems, namely mitochondrial DNA and Y chromosome have been widely employed to solve questions about origin and prehistorical range expansions, demographic processes, both in humans and domestic animals. The mtDNA and the Y chromosome, with their unique patterns of inheritance, continue to be extremely important source of information. These markers played significant roles in farm animals in the evaluation of the genetic variation within- and among-breed strains and lines and have widely applied in the fields of linkage mapping, paternity tests, prediction of breeding values in genome-assisted selection, analysis of genetic diversity within breeds detection of population admixture, assessment of inbreeding and relationships between breeds, and assignment of individuals to their breed of origin. This approach offers a unique opportunity to save genetic resources and achieving improved productivity. In the past years, significant progress was achieved in reconstructing detailed cattle phylogenies; many studies indicated multiple parental sources and several levels of phylogeographic structuring. More detailed researches are still in progress in order to provide a more comprehensive picture of such extant variability. This paper is focused on reviewing the use of the two uniparental markers as valuable tool for the characterization of cattle genetic diversity. Furthermore, their implications in animal breeding, management and genetic resources conservation are also reported.
Subject(s)
Animals , Male , Female , Cattle , Cattle/genetics , Selection, Genetic , Genetic Variation , Breeding , DNA, Mitochondrial , Genetic Markers , Demography , Domestication , Genetics, PopulationABSTRACT
Summary Background: marker assisted selection methods of sheep require the identification of genes that positively and negatively affect meat quality. Genes with high expression levels could have the greatest impact on growth and structure of muscle fibers. Objective: this study evaluated the expression of genes in the loin muscle of Dzhalginsky Merino sheep. Methods: reverse transcription-quantitative real-time PCR (RT-qPCR) was used to investigate the expression of 48 genes in the loin muscle of Dzhalginsky Merino sheep bred in Russia. Results: genes GAPDH, PYGM, CAST, ATP5G1, CAPN3, SOD1, VEGFA, CALM2, YWHAZ, ASIP,MYOD1, CAPN1, GHR, OXTR, BEGAIN, SLC2A3, and SS18L2 showed the highest expression. The group of genes with a medium level of expression included ATOX1, BAMBI, TLR6, IGF2, FOS, FST, GGTA2P, C-MET, FGF5, ACVR2A, CAPN2, GH, DGAT1, and IGF1. Low levels of expression were identified for genes ABCG2, SPP2, PYGL, PPARG2, TGFB1, CXCR4, MSTN, CYP2J, LEPR, CDKN1A, IGFBP4, and SERT. Trace expression was detected in genes SST, TSHR, GDF9, FGF7 and BMP15. Significant correlation between expression level and live weight was observed for most of the investigated genes. Conclusion: our results demonstrate the feasibility of using these newly identified candidate genes as genetic markers in sheep.
Resumen Antecedentes: los métodos de selección asistida de ovejas a través de marcadores requieren la identificación de los genes que afectan positiva o negativamente la calidad de la carne. Los genes con niveles más altos de expresión podrían tener mayor impacto en el crecimiento y estructura de las fibras musculares. Objetivo: evaluar la expresión de los genes en el músculo del lomo de carneros de la raza Dzhalginsky Merino. Métodos: se utilizó RT-PCR cuantitativa en tiempo real (RT-qPCR) para investigar la expresión de 48 genes en el músculo del lomo de ovejos raza Merino Dzhalginsky criados en Rusia. Resultados: los genes GAPDH, PYGM, CAST, ATP5G1, CAPN3, SOD1, VEGFa, CALM2, YWHAZ, ASIP, MYOD1, CAPN1, GHR, OXTR, BEGAIN,SLC2A3 y SS18L2 mostraron la más alta expresión. El grupo de genes con un nivel medio de expresión incluyó ATOX1, BAMBI, TLR6, IGF2, FOS, FST, GGTA2P, C-MET, FGF5, ACVR2A, CAPN2, GH, DGAT1 y IGF1. Se identificaron bajos niveles de expresión en los genes ABCG2, SPP2, PYGL, PPARG2, TGFB1, CXCR4, NTCR, CYP2J, LEPR, CDKN1A, IGFBP4 y SERT. Expresión traza fue detectada en los genes SST, TSHR, GDF9, FGF7 y BMP15. Para la mayoría de los genes investigados hubo una correlación significativa entre el nivel de expresión y el peso vivo de los carneros. Conclusión: los resultados demuestran la factibilidad del uso de estos genes candidatos identificados recientemente como marcadores genéticos en ovejas.
Resumo Antecedentes: métodos que utilizam marcadores de seleção assistida em ovelhas exigem a identificação de novos genes que afetam a qualidade da carne. Genes com maiores níveis de expressão podem ter maior impacto sobre o crescimento e a estrutura das fibras músculares. Objetivo: avaliar a expressão de genes no músculo lombar de ovinos da raça Merino Dzhalginsky. Métodos: foi utilizada a reação em cadeia da polimerase-transcriptase reversa e em tempo real (RT-qPCR) para investigar a expressão de 48 genes em músculo do lombo da raça de ovinos Merino Dzhalginsky, que foram criados na Rússia. Resultados: os genes GAPDH, PYGM, CAST, ATP5G1, CAPN3, SOD1, VEGFA, CALM2, YWHAZ, ASIP, MYOD1, CAPN1, GHR,OXTR, BEGAIN, SLC2A3 e SS18L2 apresentaram a maior expressão. O grupo de genes com um nível médio de expressão incluíram ATOX1, BAMBI, TLR6, IGF2, FOS, FST, GGTA2P, C-MET, FGF5, ACVR2A, CAPN2,GH, DGAT1 e IGF1. Foram identificados baixos níveis de expressão para os genes ABCG2, SPP2, PYGL, PPARG2, TGFB1, CXCR4, MSTN, CYP2J, LEPR, CDKN1A, IGFBP4 e SERT. Foi detectado rastreamento de expressão nos genes SST, TSHR, GDF9, FGF7 e BMP15. Para a maioria dos genes investigados, houve uma correlação significativa entre o nível de expressão e o peso vivo dos carneiros Dzhalginsky Merino. Conclusão: os resultados demonstram a viabilidade do uso desses genes candidatos recentemente identificados como marcadores genéticos no desenvolvimento de novas raças de ovinos.
ABSTRACT
Present study was aimed to screening the population of 25 wheat genotypes from Baluchistan region of Pakistan along with five commercial cultivars for leaf rust adult plant resistance (APR) through gene postulation using natural inoculation of Puccinia triticina Erikss local pathotype. Infection severity was recorded on scale in comparison with susceptible control "Morroco" cultivar. On the basis of phenotypic score, seven accessions and four varieties (Zardana-89, Sariab-92, Zarlashta-99 and Raskoh-05) with AUDPC values up to 20% were characterized as resistant genotypes. Coefficient of infection (CI) score ranged from 0-10 for some accessions and cultivars showing high level of adult plant resistance. Furthermore, bi-allelic STS marker csLV34 having close linkage with Lr34 (0.4cM). This marker amplified one gene specific allele of 150bp in 21 genotypes, including 19 accessions and two commercial varieties (Sariab-92 and Zarghoon-79) which confirmed presence of Lr34 gene conferring adult plant resistance against leaf rust. The rust pathogenicity scale varied for accessions from resistant to moderately susceptible. However, beside Lr34, phenotypic gene postulation, in combination with marker assisted selection for leaf rust resistance, has revealed presence of some other unknown resistance genes in local wheat germplasm which signified its use in wheat improvement programs both locally and abroad.
O presente estudo teve como objetivo a triagem da população de 25 genótipos de trigo do Baluchistão, região do Paquistão, juntamente com cinco cultivares comerciais para o estudo da resistência à ferrugem da folha em plantas adultas (leaf rust adult plant resistance, APR, em inglês) através da postulação gênica usando a inoculação natural do patótipo local da Puccinia triticina Erikks. A gravidade da infecção foi registrada na escala em comparação ao cultivar de controle suscetível "Morroco". Com base na pontuação fenotípica, sete acessões e quatro variedades (Zardana-89, Sariab-92, Zarlashta-99 and Raskoh-05) com valores de AUDPC (area under the disease progress curve, em inglês) até 20% foram caracterizados como genótipos resistentes. A pontuação do coeficiente de infecção (CI) variou no intervalo de 0-10 para algumas acessões e cultivares evidenciando uma elevada resistência nas plantas adultas. Além disso, o STS marker para o csLV34 bi-alélico demonstrou uma ligação estreita com o Lr34 (0.4cM). Este marcador amplificou um alelo específico do gene do 150bp em 21 genótipos, incluindo 19 acessões e duas variedades comerciais (Sariab-92 and Zarghoon-79) o que confirmou a presença do gene Lr34 conferindo resistência às plantas adultas contra a ferrugem da folha. A escala de patogenicidade da ferrugem para as acessões de resistente a moderadamente suscetível. Contudo, além do Lr34, a postulação gênica fenotípica, em combinação com a seleção auxiliada (ou assistida) por marcadores para a resistência da ferrugem da folha, revelou a presença de outros genes resistentes desconhecidos no germoplasma do trigo local o que justifica a sua utilização em programas de melhoramento do trigo tanto a nível local quanto a nível internacional.
Subject(s)
Triticum , Disease Resistance , Plant Pathology , GenesABSTRACT
O estudo visou inferir sobre a estabilidade genética, com base na viabilidade polínica, em genótipos de triticale hexaploide utilizados no bloco de cruzamentos do programa de melhoramento genético da Empresa Brasileira de Pesquisa Agropecuária (Embrapa Trigo). O experimento foi conduzido em delineamento inteiramente casualizado. Para cada genótipo, foram avaliadas cinco repetições e cada repetição foi constituída por uma planta. Analisaram-se, por meio de microscopia óptica e pela técnica de Squash com corante carmim acético 1%, 200 grãos de pólen por lâmina, totalizando 1.000 grãos de pólen por genótipo. As variáveis analisadas foram: grãos de pólen binucleados e trinucleados, com pouco amido, vazios, com mais de um poro e de tamanhos diferentes. Os dados obtidos foram submetidos à análise de variância e as médias comparadas pelo teste de Tukey a 1%. Houve diferença significativa entre todas as variáveis. A porcentagem de grãos de pólen binucleados e/ou trinucleados variou de 74 a 97%. Concluiu-se que 66% dos genótipos avaliados apresentaram viabilidade polínica acima de 90%, sendo indicados a continuar fazendo parte do programa de melhoramento genético de triticale, tanto na seleção de parentais como durante os cruzamentos e retrocruzamentos. Portanto, os estudos citogenéticos representam excelente ferramenta de apoio ao melhorista na escolha dos genótipos mais estáveis.(AU)
The study aimed to infer about the genetic stability from the pollen viability in hexaploid triticale genotypes used in block crossings breeding program from Brazilian Company of Agriculture Research (Embrapa Wheat). The experiments were conducted in a randomized design. For each genotype five repetitions were assessed. Each replication consisted of one plant and each replication consisted of one plant. Two hundred pollen grains were analyzed by optical microscopy and by the squash technique with 1% acetic carmine dye per slide, totalizing 1,000 pollen grains per genotype. The variables analyzed were: binucleate and trinucleate pollen grains, with little starch, empty, with more than one pore and with different sizes. The data were submitted to analysis of variance and compared by Tukey test at 1%. There were significant differences between all variables. The percentage of binucleate and/or trinucleate grains ranged from 74 to 97%. We conclude that 66% of genotypes present pollen viability above 90% and they are indicated to remain of the breeding program of triticale, both in the selection of parenting as during the crossing and backcrossing. Therefore, the cytogenetic studies represent excellent support tool for breeder in selecting the most stable genotypes.(AU)
Subject(s)
Edible Grain , Cytogenetic Analysis , Triticale/genetics , Plant Breeding , Cytological TechniquesABSTRACT
Background: molecular markers for genetic resistance can be used to control mastitis in dairy cattle. The Major Histocompatibility Complex and the Toll-like receptor 4 (TLR4) are two promising genes that warrant investigation. Objective: to identify associations between genotypes of BoLA-DRB3 locus and T4CRBR2 fragment and subclinical mastitis (SM). Methods: 996 lactating cows from 32 herds comprising Holstein (80%), Holstein x Jersey cross (12.5%), and other crosses (7.5%) were evaluated monthly during two years, diagnosed for SM and genotyped for the second exon of BoLA DRB3 and the TLR4 coreceptor-binding region 2 (T4CRBR2) using a Polymerase chain reaction-restriction fragment length polymorphism technique (PCRRFLP). The association between candidate alleles and subclinical mastitis was measured by logistic regression. Results: the most frequently observed alleles for BoLA-DRB3 were DRB3.2 *8, *22, *24, *16, *10, *23, *gba, *11, *2, *mbb, *jba, *3, and *15, accounting for 58.9% of the population. Frequencies for T4CRBR2 alleles A and B were 0.352 and 0.647, respectively. Based on 57,408 observations during the period, the mean SM prevalence was 16.2% (95% CI 13.0 and 19.4) per udder quarter and 37.6% (95% CI 32.1 and 43.2) per cow. The predominant microorganisms isolated from SM quarters were Streptococcus agalactiae and Coagulase-Negative Staphylococci (CNS). Allele DRB3.2 *23 was associated with SM occurrence and CNS infection. No alleles were associated with Streptococcus agalactiae infection. Allele *mbb was associated with occurrence of CNS infection and alleles *jba and *15 were associated with resistance to CNS infection. No significant relationship between T4CRBR2 and SM was observed. Conclusion: DRB3.2 gen may play an important role in the occurrence of SM and certain alleles may confer resistance to specific pathogens.
Antecedentes: los marcadores moleculares genéticos de resistencia para mastitis bovina son una herramienta para el control de la enfermedad en rebaños lecheros. Los genes del Complejo Mayor de Histocompatibilidad y el Receptor tipo Toll 4 (TLR4) son dos genes candidatos promisorios que justifica investigar. Objetivo: identificar asociaciones entre los genotipos del locus BoLA-DRB3 y del fragmento T4CRBR2 con la ocurrencia de mastitis subclínica. Métodos: 996 vacas lactantes de 32 hatos de las razas Holstein (80%), Holstein x Jersey (12,5%) y otros cruces (7,5%), fueron visitadas mensualmente por dos años, diagnosticadas para mastitis subclínica y genotipificadas para el segundo exón del DRB3 y para la región 2 de unión al correceptor del TLR4 (T4CRBR2) por medio de las técnicas de Reacción en cadena de la polimerasa y de Longitud del polimorfismo del fragmento de restricción (PCR-RFLP). La asociación entre los alelos candidatos y la mastitis subclínica se midió por regresión logística. Resultados: los alelos más frecuentes para el DRB3.2 fueron *8, *22, *24, *16, *10, *23, *gba, *11, *2, *mbb, *jba, *3 y *15, que suman el 58,9% del total en la población. Las frecuencias para los alelos A y B del T4CRBR2 fueron de 0,352 y 0,647, respectivamente. Basados en 57.408 observaciones, la prevalencia de MS a nivel de cuarto fue 16,2% (95% IC 13,0 y 19,4) y a nivel de vaca fue de 37,6% (95% IC 32,1 y 43,2). Los microorganismos más frecuentes fueron Streptococcus agalactiae y Estafilococo Coagulasa Negativo (ECN). El alelo DRB3.2 *23 fue el más asociado con la ocurrencia de MS y con la infección por ECN. No se hallaron alelos asociados a infección con mastitis por Streptococcus agalactiae. Con respecto a la infección por ECN, el *mbb se asoció con la ocurrencia y los alelos *jba y *15 se asociaron con resistencia. No se observó asociación entre T4CRBR2 y MS. Conclusión: el gen DRB3.2 puede jugar un papel importante en la presencia de MS y ciertos alelos pueden conferir resistencia a patógenos específicos.
Antecedentes: o uso de marcadores moleculares de resistência para mastites permite controlar esta doença em rebanhos leiteiros. Os genes Toll Like Receptor 4 (TLR4) e o Complexo Mayor de Histocompatibilidade são dois genes candidatos promissórios que justifica pesquisar. Objetivo: identificar associações entre genótipos do locus BoLA-DRB3 e do fragmento T4CRBR2 com a ocorrência de mastite subclínica. Método: 996 vacas em lactação de 32 rebanhos da raça Holandesa (80%), Holandesa x Jersey (12,5%) e outras cruzas (7,5%) foram visitadas mensalmente por dois anos, diagnosticadas para mastites subclínica e genotipadas para o exon segunda BoLA DRB3 e região 2 da ligação co-receptor TLR4 (T4CRBR2) através das técnicas de Reação em Cadeia da Polimerase e do Polimorfismo de Comprimento do Fragmento de Restrição (PCRRFLP). A associação entre alelos candidatos e mastite subclínica foi realizada por meio de regressão logística. Resultados: os alelos mais frequentes *8, *22, *24, *16, *10, *23, *gba, *11, *2, *mbb, *jba, *3 e *15, com um 58,9% do total da população. As frequências dos alelos A e B do T4CRBR2 foram 0,352 e 0,647, respectivamente. Com base em 57.408 observações, a prevalência da SM em quartos mamários foi de 16,2% ((IC 95% 13,0 e 19,4) e ao nível de vaca foi de 37,6% (IC 95% 32,1 e 43,2). Os microrganismos mais comuns foram: Streptococcus agalactiae e Estafilococos Coagulase-negativo, ECN. O alelo DRB3.2 *23 foi o mais associado com a ocorrência de SM e com a infecção por ECN. Não foram encontrados alelos associados à infecção por Streptococcus agalactiae. Em relação à infecção por ECN, o *mbb esteve associado com ocorrência e os alelos *jba e *15 estiveram associados com resistência. Não existiu associação entre MS e os alelos do T4CRBR2. Conclusão: o gene DRB3.2 bovino pode desempenhar um papel importante na presencia de MS e alguns alelos podem conferir resistência à patógenos específicos.
ABSTRACT
O milho é um dos cereais mais importantes cultivados no mundo, porém, fatores como as doenças podem ocasionar decréscimos no rendimento de grãos. A mancha branca, causada por um complexo de patógenos, está entre as principais doenças desta cultura e pode ocasionar perdas de cerca de 60 %. Dentro deste contexto, este trabalho teve como objetivos estimar parâmetros genéticos, identificar e mapear QTLs associados à resistência à mancha branca do milho, visando o desenvolvimento de genótipos resistentes à doença. Noventa e oito famílias F2:3 do cruzamento entre as linhagens BS01 (suscetível) e BS02 (resistente) e 90 famílias F2:3 do cruzamento entre BS03 (suscetível) e BS04 (resistente) foram conduzidas a campo em três ambientes. As herdabilidades variaram de 82,3 % a 86,2 % nos locais avaliados para a população 1. Para a população 2 a herdabilidade variou de 76 % a 86,6 %. Na análise conjunta para a resistência nas duas populações, efeitos entre pais e entre progênies foram significativos, assim como a interação de progênies e local, indicando que uma família superior em um local não será obrigatoriamente superior em outro local. Dos QTLs testados nas populações 1 e 2, foram encontrados marcadores que expressaram até 25% da variância fenotípica nos grupos de ligação 1, 3, 6 e 9. Assim, estes dados em conjunto demonstram a possibilidade de seleção assistida, para a resistência à mancha branca do milho, nas gerações iniciais com o uso dos marcadores moleculares estudados.
Maize is one of the most important cereal crops in the world; however, diseases, among other factors, may drastically reduce its grain yield. The white spot disease, caused by a complex of pathogens, is one of the most important syndromes affecting maize, causing losses of up to 60%. Thus, this study aimed to estimate heritability, to identify and to map QTLs associated with resistance to white spot in maize. Ninety-eight F2:3 families from a cross between lines BS01 (susceptible) and BS02 (resistant) and ninety F2:3 families from a cross between BS03 (susceptible) and BS04 (resistant) were evaluated in a lattice square (10x10) experimental design in three environments. Heritability estimations ranged from 82.3% to 86.2% in population 1, and from 76% to 86.6% in population 2. A joint analysis of both populations showed significant effects among parents and progenies, so it did for the interactions of locations and progenies. It means that a specific family may not show the same performance for resistance to white spot across different environments. QTLs for resistance to white spot were found in the linkage groups 1, 3, 6 and 9 in both populations. These QTLs explained up to 25% of the total phenotypic variation for the studied trait. Combined, these data confirm the possibility of marker assisted selection for resistance to maize white spot in early generations.
Subject(s)
Zea mays , Fungi , Fungicides, IndustrialABSTRACT
The aim of this study was to evaluate genetic diversity of nine molecular markers, six short tandem repeats - STRs (BM4325, BMS3004, ILSTS002, IDVGA51, HEL5, AFZ1) and three single nucleotide polymorphisms (SNPs; LepSau3A1 A-B, LepSau3A1 1-2, and FSHRAlu1), linked to genes involved in reproductive function and their possible effect on reproductive performance. For this purpose, 81 crossbred beef cows were used in this study. The animals were classified into two groups (fertile and sub-fertile cows) based on their pregnancy status after two breeding seasons. High genetic diversity level was observed highlighted by the polymorphic content information ranging 0.23 to 0.87 and expected heterozygosity from 27 to 89%, with an average of 62%. Alleles BM4325 103, BMS3004 129, ILSTS002 137, IDVGA51 177, LEPSau3A1 A, LEPSau3A1 1, HEL5 149, AFZ1 119 and FSHRAlu1 G presented high frequencies. Two STRs (IDVGA51 and ILSTS002), linked to Leptin and LH genes, respectively, were associated to reproductive performance. These data support previous findings suggesting the potential use of IDVGA51 and ILSTS002 STRs for reproductive performance selection.
Foi avaliada a diversidade genética de nove marcadores moleculares, dos quais seis do tipo short tandem repeats - STR (BM4325, BMS3004, ILSTS002, IDVGA51, HEL5, AFZ1) e três do tipo single nucleotide polymorphisms - SNPs (LepSau3A1 A-B, LepSau3A1 1-2 e FSHRAlu1), ligados a genes envolvidos na reprodução e seus efeitos na performance reprodutiva. Foram examinadas amostras de sangue de 81 vacas sem raça definida, os animais foram classificados em dois grupos (vacas férteis e subférteis) baseado nas taxas de prenhez de duas estações reprodutivas. Alto nível de diversidade genética foi observado, revelando alto conteúdo de informação polimórfica, variando de 0,23 a 0,87 e heterozigosidade esperada de 27 a 89% com 62% em média. Os alelos mais frequentes foram BM4325 103*, BMS3004 129*, ILSTS002 137*, IDVGA51 177*, LEPSau3A1 A, LEPSau3A1 1, HEL5 149*, AFZ1 119* e FSHRAlu1 G. Os marcadores IDVGA51 e ILSTS002, ligados aos genes da leptina e LH, respectivamente, foram associados a performance reprodutiva. Esses dados suportam achados prévios que sugerem o potencial uso desses marcadores na seleção de animais com maior performance reprodutiva.
Subject(s)
Animals , Female , Pregnancy , Cattle , Luteinizing Hormone, beta Subunit/genetics , Leptin/genetics , Polymorphism, Single Nucleotide/genetics , Tandem Repeat Sequences/genetics , Genetic Variation/genetics , Reproductive Techniques, Assisted/veterinaryABSTRACT
Molecular markers may accelerate selection through the identification of plants with higher proportion of recurrent parent genome, as well as identifying those plants bearing target alleles like quantitative traits loci (QTLs) for white mold resistance. The objectives of this work were: 1) to employ microsatellite markers (SSR) in order to accelerate the recovery of recurrent parent genome 2) to validate sequence characterized amplified region (SCAR) Phs associated with a QTL that confers resistance to white mold, as previously identified in bean populations. Lines G122 and M20 were crossed, which generated 267 F1 plants from backcross (BC) BC1 and 113 plants from backcross BC2.SSR polymorphic markers were adopted. The relationship between BC plants and the recurrent parent was estimated based on the recurrent genome proportion (PR) in each BC plant, and the Sorensen-Dice genetic similarity (sg ir). To determine how much the phenotypic variation is explained by SCAR Phs, 56 F1:2BC1 progenies were evaluated on the field following a random block design with two replications through the straw test method. SSR markers are efficient in identifying individuals with a greater proportion of the recurrent genome. SCAR Phs was not efficient for the indirect selection of common beans for white mold resistance.