Construction and application of SSR molecular markers system for genetic diversity analysis of Chinese tartary buckwheat germplasm resources

[Objective] The SSR molecular markers system was optimized and constructed for genetic diversity analyses of Chinese tartary buckwheat germplasm resources,which is helpful for evaluating Chinese tartary buckwheat collections.[Method] The SSR-PCR system was optimized by [L16(45)]orthogonal design,the...

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Autores principales: Gao F, Zhang, Z., Wu B.
Formato: Journal Article
Lenguaje:Inglés
Publicado: 2012
Materias:
Acceso en línea:https://hdl.handle.net/10568/34961
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author Gao F
Zhang, Z.
Wu B.
author_browse Gao F
Wu B.
Zhang, Z.
author_facet Gao F
Zhang, Z.
Wu B.
author_sort Gao F
collection Repository of Agricultural Research Outputs (CGSpace)
description [Objective] The SSR molecular markers system was optimized and constructed for genetic diversity analyses of Chinese tartary buckwheat germplasm resources,which is helpful for evaluating Chinese tartary buckwheat collections.[Method] The SSR-PCR system was optimized by [L16(45)]orthogonal design,the optimized gel concentration of PAGE was confirmed,and the genetic diversity of 50 tartary buckwheat accessions was analyzed by 19 SSR primer pairs screened from 250 ones of different crops.[Result]The optimized SSR-PCR system was as follows: 30 ng DNA template,150 μmol?L-1 dNTP,0.1 μmol?L-1 primer,2.0 U?L-1 TaqDNA polymerase,2.0 mmol?L-1 Mg2+,1×Taq buffer and ddH2O then added up to terminal volume of 25 μL with 6% PAGE for testing.The primers screening efficiency was 7.6%,and the primers from common buckwheat were applicable.A total of 157 alleles were detected by 19 primers,with 2-11 alleles for each primer pair,and the average was 7.42.Moreover,the averaged PIC and DP values were 0.8881 and 5.684,respectively.Using Popgen Ver.1.31,50 accessions were clustered into 5 groups at GS 0.578.The clustering results revealed that the genetic diversity of accessions of tartary buckwheat was not correlated to their geographic origins.The genetic diversity of tartary buckwheat from Sichuan was very rich as genetic parameters were the highest.The core primers could be used to identify the similar accessions.[Conclusion] The SSR molecular markers system was effective for assessment of genetic diversity of Chinese tartary buckwheat germplasm resources.SSR primers of common buckwheat could be used in tartary buckwheat.TBP5 and Fes2695 were SSR core primers.It showed a high genetic diversity in 50 Chinese tartary buckwheat accessions which could be classified into 5 groups.
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spelling CGSpace349612023-06-12T13:37:16Z Construction and application of SSR molecular markers system for genetic diversity analysis of Chinese tartary buckwheat germplasm resources Gao F Zhang, Z. Wu B. agriculture climate germplasm [Objective] The SSR molecular markers system was optimized and constructed for genetic diversity analyses of Chinese tartary buckwheat germplasm resources,which is helpful for evaluating Chinese tartary buckwheat collections.[Method] The SSR-PCR system was optimized by [L16(45)]orthogonal design,the optimized gel concentration of PAGE was confirmed,and the genetic diversity of 50 tartary buckwheat accessions was analyzed by 19 SSR primer pairs screened from 250 ones of different crops.[Result]The optimized SSR-PCR system was as follows: 30 ng DNA template,150 μmol?L-1 dNTP,0.1 μmol?L-1 primer,2.0 U?L-1 TaqDNA polymerase,2.0 mmol?L-1 Mg2+,1×Taq buffer and ddH2O then added up to terminal volume of 25 μL with 6% PAGE for testing.The primers screening efficiency was 7.6%,and the primers from common buckwheat were applicable.A total of 157 alleles were detected by 19 primers,with 2-11 alleles for each primer pair,and the average was 7.42.Moreover,the averaged PIC and DP values were 0.8881 and 5.684,respectively.Using Popgen Ver.1.31,50 accessions were clustered into 5 groups at GS 0.578.The clustering results revealed that the genetic diversity of accessions of tartary buckwheat was not correlated to their geographic origins.The genetic diversity of tartary buckwheat from Sichuan was very rich as genetic parameters were the highest.The core primers could be used to identify the similar accessions.[Conclusion] The SSR molecular markers system was effective for assessment of genetic diversity of Chinese tartary buckwheat germplasm resources.SSR primers of common buckwheat could be used in tartary buckwheat.TBP5 and Fes2695 were SSR core primers.It showed a high genetic diversity in 50 Chinese tartary buckwheat accessions which could be classified into 5 groups. 2012 2014-02-19T07:59:26Z 2014-02-19T07:59:26Z Journal Article https://hdl.handle.net/10568/34961 en Limited Access Gao F, Zhang Z, Wu B. 2012. Construction and application of SSR molecular markers system for genetic diversity analysis of Chinese tartary buckwheat germplasm resources. Scientia Agricultura Sinica 45(6): 1042–1053.
spellingShingle agriculture
climate
germplasm
Gao F
Zhang, Z.
Wu B.
Construction and application of SSR molecular markers system for genetic diversity analysis of Chinese tartary buckwheat germplasm resources
title Construction and application of SSR molecular markers system for genetic diversity analysis of Chinese tartary buckwheat germplasm resources
title_full Construction and application of SSR molecular markers system for genetic diversity analysis of Chinese tartary buckwheat germplasm resources
title_fullStr Construction and application of SSR molecular markers system for genetic diversity analysis of Chinese tartary buckwheat germplasm resources
title_full_unstemmed Construction and application of SSR molecular markers system for genetic diversity analysis of Chinese tartary buckwheat germplasm resources
title_short Construction and application of SSR molecular markers system for genetic diversity analysis of Chinese tartary buckwheat germplasm resources
title_sort construction and application of ssr molecular markers system for genetic diversity analysis of chinese tartary buckwheat germplasm resources
topic agriculture
climate
germplasm
url https://hdl.handle.net/10568/34961
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