Evidence map›Paper›PMID 41493480›Full record

ArticleMolecular biology reports2026

Development of SCAR and rapid detection of YMV resistant genotypes of blackgram through qRT-PCR based absolute quantification.

Priyanka Halldakeri, Amar A Sakure, Sushil Kumar, Sneha Macwana, K V Patel, D A Patel

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Article in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Priyanka HalldakeriDepartment of Genetics and Plant Breeding, Anand Agricultural University, Anand, Gujarat, India.
Amar A SakureDepartment of Agriculture Biotechnology, Anand Agricultural University, Anand, Gujarat, India. amar_biotech@aau.in.
Sushil KumarDepartment of Agriculture Biotechnology, Anand Agricultural University, Anand, Gujarat, India.
Sneha MacwanaDepartment of Genetics and Plant Breeding, Anand Agricultural University, Anand, Gujarat, India.
K V PatelCrop Improvement Division, ICARVIVEKANANDAPARVATIYA KRISHI ANUSANDHAN SANSTHAN, Almora, Uttarakhand, India.
D A PatelDepartment of Agriculture Biotechnology, Anand Agricultural University, Anand, Gujarat, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Black gram [Vigna mungo (L.) Hepper] is an important food legume whose productivity in the Indian subcontinent has declined due to multiple abiotic and biotic stresses, particularly Yellow Mosaic Virus (YMV), a major yield-limiting pathogen. To support the development of YMV-resistant varieties, the present study aimed to identify reliable molecular markers associated with YMV resistance. A bi-parental mapping population was developed from two contrasting genotypes-NUK 17 - 05 (highly resistant) and VUG 49 (highly susceptible)-and subjected to bulked segregant analysis using RAPD markers. A polymorphic RAPD marker (OPAD17) linked to resistance was identified and subsequently converted into a stable SCAR marker, designated SCAR15 (238 bp). SCAR15 consistently differentiated resistant and susceptible parents based on band intensity and was validated using F₂ individuals representing extreme phenotypes. qRT-PCR analysis confirmed that resistance was associated with copy number variation at the SCAR15 locus. Resistant lines showed a copy number > 0.1 with a mean value of 1.85, whereas susceptible lines had a mean copy number of 0.06. These results demonstrate that YMV resistance in the studied population is linked to genomic copy number variation. The SCAR15 marker developed in this study provides a robust tool for marker-assisted selection and breeding of YMV-resistant black gram genotypes.

Indexed as

Disease ResistancePlant DiseasesVignaDNA Copy Number VariationsGenetic MarkersGenotypeRandom Amplified Polymorphic DNA TechniqueReal-Time Polymerase Chain ReactionGenetic MarkersBlack gramRAPDRT-PCRSCARYMV

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.