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Identification of SNP and SSR Markers in Finger Millet Using Next Generation Sequencing Technologies

Finger millet is an important cereal crop in eastern Africa and southern India with excellent grain storage quality and unique ability to thrive in extreme environmental conditions. Since negligible attention has been paid to improving this crop to date, the current study used Next Generation Sequen...

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Autores principales: Gimode, Davis, Odeny, Damaris A., de Villiers, Etienne P., Wanyonyi, Solomon, Dida, Mathews M., Mneney, Emmarold E., Muchugi, Alice, Machuka, Jesse, de Villiers, Santie M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959724/
https://www.ncbi.nlm.nih.gov/pubmed/27454301
http://dx.doi.org/10.1371/journal.pone.0159437
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author Gimode, Davis
Odeny, Damaris A.
de Villiers, Etienne P.
Wanyonyi, Solomon
Dida, Mathews M.
Mneney, Emmarold E.
Muchugi, Alice
Machuka, Jesse
de Villiers, Santie M.
author_facet Gimode, Davis
Odeny, Damaris A.
de Villiers, Etienne P.
Wanyonyi, Solomon
Dida, Mathews M.
Mneney, Emmarold E.
Muchugi, Alice
Machuka, Jesse
de Villiers, Santie M.
author_sort Gimode, Davis
collection PubMed
description Finger millet is an important cereal crop in eastern Africa and southern India with excellent grain storage quality and unique ability to thrive in extreme environmental conditions. Since negligible attention has been paid to improving this crop to date, the current study used Next Generation Sequencing (NGS) technologies to develop both Simple Sequence Repeat (SSR) and Single Nucleotide Polymorphism (SNP) markers. Genomic DNA from cultivated finger millet genotypes KNE755 and KNE796 was sequenced using both Roche 454 and Illumina technologies. Non-organelle sequencing reads were assembled into 207 Mbp representing approximately 13% of the finger millet genome. We identified 10,327 SSRs and 23,285 non-homeologous SNPs and tested 101 of each for polymorphism across a diverse set of wild and cultivated finger millet germplasm. For the 49 polymorphic SSRs, the mean polymorphism information content (PIC) was 0.42, ranging from 0.16 to 0.77. We also validated 92 SNP markers, 80 of which were polymorphic with a mean PIC of 0.29 across 30 wild and 59 cultivated accessions. Seventy-six of the 80 SNPs were polymorphic across 30 wild germplasm with a mean PIC of 0.30 while only 22 of the SNP markers showed polymorphism among the 59 cultivated accessions with an average PIC value of 0.15. Genetic diversity analysis using the polymorphic SNP markers revealed two major clusters; one of wild and another of cultivated accessions. Detailed STRUCTURE analysis confirmed this grouping pattern and further revealed 2 sub-populations within wild E. coracana subsp. africana. Both STRUCTURE and genetic diversity analysis assisted with the correct identification of the new germplasm collections. These polymorphic SSR and SNP markers are a significant addition to the existing 82 published SSRs, especially with regard to the previously reported low polymorphism levels in finger millet. Our results also reveal an unexploited finger millet genetic resource that can be included in the regional breeding programs in order to efficiently optimize productivity.
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spelling pubmed-49597242016-08-08 Identification of SNP and SSR Markers in Finger Millet Using Next Generation Sequencing Technologies Gimode, Davis Odeny, Damaris A. de Villiers, Etienne P. Wanyonyi, Solomon Dida, Mathews M. Mneney, Emmarold E. Muchugi, Alice Machuka, Jesse de Villiers, Santie M. PLoS One Research Article Finger millet is an important cereal crop in eastern Africa and southern India with excellent grain storage quality and unique ability to thrive in extreme environmental conditions. Since negligible attention has been paid to improving this crop to date, the current study used Next Generation Sequencing (NGS) technologies to develop both Simple Sequence Repeat (SSR) and Single Nucleotide Polymorphism (SNP) markers. Genomic DNA from cultivated finger millet genotypes KNE755 and KNE796 was sequenced using both Roche 454 and Illumina technologies. Non-organelle sequencing reads were assembled into 207 Mbp representing approximately 13% of the finger millet genome. We identified 10,327 SSRs and 23,285 non-homeologous SNPs and tested 101 of each for polymorphism across a diverse set of wild and cultivated finger millet germplasm. For the 49 polymorphic SSRs, the mean polymorphism information content (PIC) was 0.42, ranging from 0.16 to 0.77. We also validated 92 SNP markers, 80 of which were polymorphic with a mean PIC of 0.29 across 30 wild and 59 cultivated accessions. Seventy-six of the 80 SNPs were polymorphic across 30 wild germplasm with a mean PIC of 0.30 while only 22 of the SNP markers showed polymorphism among the 59 cultivated accessions with an average PIC value of 0.15. Genetic diversity analysis using the polymorphic SNP markers revealed two major clusters; one of wild and another of cultivated accessions. Detailed STRUCTURE analysis confirmed this grouping pattern and further revealed 2 sub-populations within wild E. coracana subsp. africana. Both STRUCTURE and genetic diversity analysis assisted with the correct identification of the new germplasm collections. These polymorphic SSR and SNP markers are a significant addition to the existing 82 published SSRs, especially with regard to the previously reported low polymorphism levels in finger millet. Our results also reveal an unexploited finger millet genetic resource that can be included in the regional breeding programs in order to efficiently optimize productivity. Public Library of Science 2016-07-25 /pmc/articles/PMC4959724/ /pubmed/27454301 http://dx.doi.org/10.1371/journal.pone.0159437 Text en © 2016 Gimode et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Gimode, Davis
Odeny, Damaris A.
de Villiers, Etienne P.
Wanyonyi, Solomon
Dida, Mathews M.
Mneney, Emmarold E.
Muchugi, Alice
Machuka, Jesse
de Villiers, Santie M.
Identification of SNP and SSR Markers in Finger Millet Using Next Generation Sequencing Technologies
title Identification of SNP and SSR Markers in Finger Millet Using Next Generation Sequencing Technologies
title_full Identification of SNP and SSR Markers in Finger Millet Using Next Generation Sequencing Technologies
title_fullStr Identification of SNP and SSR Markers in Finger Millet Using Next Generation Sequencing Technologies
title_full_unstemmed Identification of SNP and SSR Markers in Finger Millet Using Next Generation Sequencing Technologies
title_short Identification of SNP and SSR Markers in Finger Millet Using Next Generation Sequencing Technologies
title_sort identification of snp and ssr markers in finger millet using next generation sequencing technologies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959724/
https://www.ncbi.nlm.nih.gov/pubmed/27454301
http://dx.doi.org/10.1371/journal.pone.0159437
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