Journals / Turkish Journal of Biology / 2015 / Cilt: 39 - Sayı: 5

Discovery of Dhn3 variants in wild barley (Hordeum spontaneum) byhigh-resolution melting (HRM) technology

Pages
758–764
Publication Date
2015-12-04
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The conditions and parameters for an optimized HRM assay were outlined, and its potential application in allelic variation research of stress-related genes was discussed.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Abstract: The analysis of allelic variation in model plant species and their wild relatives, such as Hordeum vulgare and Hordeum spontaneum, is useful for relating genetic determinants and important phenotypic traits such as stress tolerance.
📊
Key Findings & Data:The present study describes an HRM analysis of natural sequence variation within Dhn3 alleles from different H. spontaneum accessions.
💡
Conclusion & Impact:The conditions and parameters for an optimized HRM assay were outlined, and its potential application in allelic variation research of stress-related genes was discussed.
🔬Design:Modeling & Simulation
📍Scope:Comprehensive Sample
⚙️Variables:High-resolution melting · wild barley · Dhn3

Abstract

Abstract: The analysis of allelic variation in model plant species and their wild relatives, such as Hordeum vulgare and Hordeum spontaneum, is useful for relating genetic determinants and important phenotypic traits such as stress tolerance. High resolution melting (HRM) analysis is a cost-effective, rapid, and high-throughput assay for mutation screening and genotyping without sequencing. The present study describes an HRM analysis of natural sequence variation within Dhn3 alleles from different H. spontaneum accessions. Small PCR-derived amplicon assays were developed for exon 1 and exon 2 of Dhn3. The efficiency of the HRM procedure was affected by various factors, including specificity and efficiency of PCR, amplicon length and position, and DNA template quality. In addition to these factors, the use of PCR product rather than genomic DNA in HRM increased the quality of melting curves, thus affecting the accuracy and sensitivity of the assay. HRM classified 5-6 groups of variants carrying deletion mutants and single and multiple SNPs consistent with the sequencing data. 18-bp deletion variants were distinguished from the reference sample according to HRM analysis of 207-bp fragment of exon 1. A/T conversions were difficult to discriminate variants, whereas A/G or T/C transitions were easily grouped because they required high Tm differences. The conditions and parameters for an optimized HRM assay were outlined, and its potential application in allelic variation research of stress-related genes was discussed.

Özet

Abstract: The analysis of allelic variation in model plant species and their wild relatives, such as Hordeum vulgare and Hordeum spontaneum, is useful for relating genetic determinants and important phenotypic traits such as stress tolerance. High resolution melting (HRM) analysis is a cost-effective, rapid, and high-throughput assay for mutation screening and genotyping without sequencing. The present study describes an HRM analysis of natural sequence variation within Dhn3 alleles from different H. spontaneum accessions. Small PCR-derived amplicon assays were developed for exon 1 and exon 2 of Dhn3. The efficiency of the HRM procedure was affected by various factors, including specificity and efficiency of PCR, amplicon length and position, and DNA template quality. In addition to these factors, the use of PCR product rather than genomic DNA in HRM increased the quality of melting curves, thus affecting the accuracy and sensitivity of the assay. HRM classified 5-6 groups of variants carrying deletion mutants and single and multiple SNPs consistent with the sequencing data. 18-bp deletion variants were distinguished from the reference sample according to HRM analysis of 207-bp fragment of exon 1. A/T conversions were difficult to discriminate variants, whereas A/G or T/C transitions were easily grouped because they required high Tm differences. The conditions and parameters for an optimized HRM assay were outlined, and its potential application in allelic variation research of stress-related genes was discussed.

🔖

Cite This Article

UÇARLI, C., POYRAZ, N., GÜREL, A. F. (2015). Discovery of Dhn3 variants in wild barley (Hordeum spontaneum) byhigh-resolution melting (HRM) technology. Turkish Journal of Biology, Cilt: 39 - Sayı: 5, 758–764. https://ajindex.com/articles/181493

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (11)

  1. Botticella E, Sestili F, Hernandez-Lopez A, Phillips A, Lafiandra D (2011). High resolution melting analysis for the detection of EMS induced mutations in wheat SbeIIa genes. BMC Plant Biol 11: 156–170.
  2. Carillo S, Henry L, Lippert E, Girodon F, Guiraud I, Richard C, Dubois Galopin F, Cleyrat C, Jourdan E, Kralovics R et al. (2011). Nested high-resolution melting curve analysis a highly sensitive, reliable, and simple method for detection of JAK2 exon 12 mutations—clinical relevance in the monitoring of polycythemia. J Mol Diagn 13: 263–270.
  3. Choi DW, Zhu B, Close TJ (1999). The barley (Hordeum vulgare L.) dehydrin multigene family: sequences, allele types, chromosome assignments, and expression characteristics of 11 Dhn genes of cv Dicktoo. Theor Appl Genet 98: 1234–1247.
  4. Cousins MM, Ou SS, Wawer MJ, Munshaw S, Swan D, Magaret CA, Mullis CE, Serwadda D, Porcella SF, Gray RH et al. (2012). Comparison of a high-resolution melting assay to next- generation sequencing for analysis of HIV diversity. J Clin Microbiol 50: 3054–3059.
  5. Er TK, Chang JG (2012). High-resolution melting: applications in genetic disorders. Clin Chim Acta 414: 197–201.
  6. Garg R, Varshney RK, Jain M (2014). Molecular genetics and genomics of abiotic stress responses. Front Plant Sci 5: 398– 400. Gundry CN, Dobrowolski SF, Martin YR, Robbins TC, Nay LM, Boyd N, Coyne T, Wall MD, Wittwer CT, Teng DH (2008). Base-pair neutral homozygotes can be discriminated by calibrated high- resolution melting of small amplicons. Nucleic Acids Res 36: 3401–3408.
  7. Guo P, Baum M, Grando S, Ceccarelli S, Bai G, Li R, von Korff M, Varshney RK, Graner A, Valkoun J (2009). Differentially expressed genes between drought-tolerant and drought- sensitive barley genotypes in response to drought stress during the reproductive stage. J Exp Bot 60: 3531–3544.
  8. Harlan JR, Zohary D (1966). Distribution of wild wheats and barley. Science 153: 1074–1080.
  9. Hofinger BJ, Jing HC, Hammond-Kosack KE, Kanyuka K (2009). High-resolution melting analysis of cDNA-derived PCR amplicons for rapid and cost-effective identification of novel alleles in barley. Theor Appl Genet 119: 851–865.
  10. Karami A, Shahbazi M, Niknam V, Shobbar ZS, Tafreshi RS, Abedini R, Mabood HE (2013). Expression analysis of dehydrin multigene family across tolerant and susceptible barley (Hordeum vulgare L.) genotypes in response to terminal drought stress. Acta Physiol Plant 35: 2289–2297.
  11. Lehmensiek A, Sutherland MW, McNamara RB (2008). The use of high resolution melti