marker assisted selection
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2022 ◽  
pp. 1-6
Author(s):  
Susheel Sharma ◽  
Aejaz Ahmad Dar ◽  
Sachin Gupta ◽  
Ravinder Singh

Abstract Powdery mildew (PM) is one of the most severe fungal diseases of cucumber that limits its production worldwide. In this study, 140 genotypes of cucumber were screened for disease resistance under field and artificial conditions, and then validated with eight known SSR markers linked to PM resistance. Among these genotypes, genotype GS140 was found resistant (R), whereas GS148, GS16 and GS70 were moderately resistant, and GS169 was found to be tolerant. Of all the eight markers, only C31, C80, C162, SSR16472 and SSR16881 amplified the reported linked allele. The 127 bp allele of SSR16881 was found to be associated with the lowest disease severity of 37.65%. The associated markers could further be verified for their usability using linkage studies and the contrast genotypes in the present study could serve as a tool for selection in future marker-assisted selection breeding strategies for PM resistance.


Biology ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 49
Author(s):  
Samathmika Ravi ◽  
Mahdi Hassani ◽  
Bahram Heidari ◽  
Saptarathi Deb ◽  
Elena Orsini ◽  
...  

Rhizoctonia solani, causing Rhizoctonia crown and root rot, is a major risk to sugar beet (Beta vulgaris L.) cultivation. The development of resistant varieties accelerated by marker-assisted selection is a priority of breeding programs. We report the identification of a single-nucleotide polymorphism (SNP) marker linked to Rhizoctonia resistance using restriction site-associated DNA (RAD) sequencing of two geographically discrete sets of plant materials with different degrees of resistance/susceptibility to enable a wider selection of superior genotypes. The variant calling pipeline utilized SAMtools for variant calling and the resulting raw SNPs from RAD sequencing (15,988 and 22,439 SNPs) were able to explain 13.40% and 25.45% of the phenotypic variation in the two sets of material from different sources of origin, respectively. An association analysis was carried out independently on both the datasets and mutually occurring significant SNPs were filtered depending on their contribution to the phenotype using principal component analysis (PCA) biplots. To provide a ready-to-use marker for the breeding community, a systematic molecular validation of significant SNPs distributed across the genome was undertaken to combine high-resolution melting, Sanger sequencing, and rhAmp SNP genotyping. We report that RsBv1 located on Chromosome 6 (9000093 bp) is significantly associated with Rhizoctonia resistance (p < 0.01) and able to explain 10% of the phenotypic disease variance. The related SNP assay is thus ready for marker-assisted selection in sugar beet breeding for Rhizoctonia resistance.


2021 ◽  
Vol 12 ◽  
Author(s):  
Fakhriddin N. Kushanov ◽  
Ozod S. Turaev ◽  
Dilrabo K. Ernazarova ◽  
Bunyod M. Gapparov ◽  
Barno B. Oripova ◽  
...  

Cotton genetic resources contain diverse economically important traits that can be used widely in breeding approaches to create of high-yielding elite cultivars with superior fiber quality and adapted to biotic and abiotic stresses. Nevertheless, the creation of new cultivars using conventional breeding methods is limited by the cost and proved to be time consuming process, also requires a space to make field observations and measurements. Decoding genomes of cotton species greatly facilitated generating large-scale high-throughput DNA markers and identification of QTLs that allows confirmation of candidate genes, and use them in marker-assisted selection (MAS)-based breeding programs. With the advances of quantitative trait loci (QTL) mapping and genome-wide-association study approaches, DNA markers associated with valuable traits significantly accelerate breeding processes by replacing the selection with a phenotype to the selection at the DNA or gene level. In this review, we discuss the evolution and genetic diversity of cotton Gossypium genus, molecular markers and their types, genetic mapping and QTL analysis, application, and perspectives of MAS-based approaches in cotton breeding.


2021 ◽  
pp. 85-94
Author(s):  
Sushma Tiwari ◽  
M. K. Tripathi ◽  
R. S. Tomar ◽  
Ashok Ahuja

Genes ◽  
2021 ◽  
Vol 12 (12) ◽  
pp. 1985
Author(s):  
Elizabeth Esdaile ◽  
Angelica Kallenberg ◽  
Felipe Avila ◽  
Rebecca R. Bellone

Coat color is a trait of economic significance in horses. Variants in seven genes have been documented to cause white patterning in horses. Of the 34 variants that have been identified in KIT proto-oncogene, receptor tyrosine kinase (KIT), 27 have only been reported in a single individual or family and thus not all are routinely offered for genetic testing. Therefore, to enable proper use of marker-assisted selection, determining breed specificity for these alleles is warranted. Screening 19 unregistered all-white Shetland ponies for 16 white patterning markers identified 14 individuals whose phenotype could not be explained by testing results. In evaluating other known dominant white variants, 14 horses were heterozygous for W13. W13 was previously only reported in two quarter horses and a family of Australian miniature horses. Genotyping known white spotting variants in 30 owner-reported white animals (25 Miniature Horses and five Shetland ponies) identified two additional W13/N American Miniature Horses. The estimated allele frequency of W13 in the American Miniature Horse was 0.0063 (79 N/N, 1 W13/N) and the allele was not detected in a random sample (n = 59) of Shetland ponies. No homozygous W13 individuals were identified and W13/N ponies had a similar all-white coat with pink skin phenotype, regardless of the other white spotting variants present, demonstrating that W13 results in a Mendelian inherited dominant white phenotype and homozygosity is likely lethal. These findings document the presence of W13 in the American Miniature Horse and Shetland pony populations at a low frequency and illustrate the importance of testing for this variant in additional breeds.


2021 ◽  
pp. 119-136
Author(s):  
P.M. Visscher ◽  
S. Van der Beek ◽  
C.S. Haley

Biology ◽  
2021 ◽  
Vol 10 (12) ◽  
pp. 1249
Author(s):  
Andekelile Mwamahonje ◽  
John Saviour Yaw Eleblu ◽  
Kwadwo Ofori ◽  
Santosh Deshpande ◽  
Tileye Feyissa ◽  
...  

Sorghum is an important staple food crop in drought prone areas of Sub-Saharan Africa, which is characterized by erratic rainfall with poor distribution. Sorghum is a drought-tolerant crop by nature with reasonable yield compared to other cereal crops, but such abiotic stress adversely affects the productivity. Some sorghum varieties maintain green functional leaves under post-anthesis drought stress referred to as stay-green, which makes it an important crop for food and nutritional security. Notwithstanding, it is difficult to maintain consistency of tolerance over time due to climate change, which is caused by human activities. Drought in sorghum is addressed by several approaches, for instance, breeding drought-tolerant sorghum using conventional and molecular technologies. The challenge with conventional methods is that they depend on phenotyping stay-green, which is complex in sorghum, as it is constituted by multiple genes and environmental effects. Marker assisted selection, which involves the use of DNA molecular markers to map QTL associated with stay-green, has been useful to supplement stay-green improvement in sorghum. It involves QTL mapping associated with the stay-green trait for introgression into the senescent sorghum varieties through marker-assisted backcrossing by comparing with phenotypic field data. Therefore, this review discusses mechanisms of drought tolerance in sorghum focusing on physiological, morphological, and biochemical traits. In addition, the review discusses the application of marker-assisted selection techniques, including marker-assisted backcrossing, QTL mapping, and QTL pyramiding for addressing post-flowering drought in sorghum.


2021 ◽  
Author(s):  
Arsalan Barazandeh ◽  
Morteza Mokhtari ◽  
Zahra Roudbari ◽  
Rouhollah Mirmahmoudi

Abstract Litter size is perhaps the main commercial trait since it has an observable effect on benefit in the sheep industry. Fecundity genes, play a vital role in expression of litter size. One of the most popular of these genes is the Booroola gene (FecB). In many past researches there was a dependency between the BMPR1B gene polymorphism and litter size of sheep. In the current study, a meta-analysis directed by coalescing outcoming of 9902 cases of 26 published research wherein various breeds of sheep to assess the influence of the FecB gene on litter size utilizing additive, recessive, dominant, and co-dominant genetic models. The random effects model was used for data analysis according to the Cochran Q test and I2 quantity. Under additive (SMD = 0.528), dominant (SMD = 0.468) and recessive (SMD = 0.250) models, the significant effect (P<0.01) of FecB genotypes has been identified. Furthermore, under the co-dominant (SMD = -0.050, P = 0.3332) model, the association between FecB genotypes and litter size trait had not been detected. A growth in litter size by about 0.47 lambs (Dominant model) was associated with the first copy of the FecB gene and 0.25 lambs (Recessive model) with the second copy of this gene. Consequences of the current study support the idea that BMPR1B fundamentally influenced litter size and subsequently it may be utilized for Marker-assisted selection programmers for improved genetic merit of reproductive futures and furthermore insert this gene by crossbreeding in low prolific breeds may improve reproductive characteristics.


Author(s):  
Georgeta BIVOLARIU (GUZU) ◽  
Ioan ZAGRAI ◽  
Luminița ZAGRAI ◽  
Mirela Irina CORDEA ◽  
Claudiu MOLDOVAN

Apple scab, caused by Venturia inaequalis is one of the most damaging pathogens that affects apple species. Cross combinations were made between Auriu de Bistrița cv. (female genitor) - a valuable local variety in terms of fruit quality but only tolerant to scab, and Florina cv. (male genitor) used as a donor of Vf resistance gene. It was first detected in Malus floribunda Clone 821, which was later transferred to commercial varieties by different breeding programs. To confirm the presence of Vf gene, progenies resulting from the mentioned combination were tested with MAS (Marker Assited Selection), using two dominant primers pairs (AM19, U1400), and another one codominant (AL07) used to distinguish homozygous and heterozygous genotypes. After the crossing combination, a number of twenty-six hybrids were obtained, of which 50% (13 hybrids) were clasified as resistant (heterozygous), respectively 50% (13 hybrids) as susceptible (recessive homozygotes), so the Mendelian ratio was confirmed.


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