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Gene Classification and Mining of Molecular Markers Useful in Red Clover (Trifolium pratense) Breeding

Red clover (Trifolium pratense) is an important forage plant worldwide. This study was directed to broadening current knowledge of red clover's coding regions and enhancing its utilization in practice by specific reanalysis of previously published assembly. A total of 42,996 genes were characte...

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Autores principales: Ištvánek, Jan, Dluhošová, Jana, Dluhoš, Petr, Pátková, Lenka, Nedělník, Jan, Řepková, Jana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360756/
https://www.ncbi.nlm.nih.gov/pubmed/28382043
http://dx.doi.org/10.3389/fpls.2017.00367
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author Ištvánek, Jan
Dluhošová, Jana
Dluhoš, Petr
Pátková, Lenka
Nedělník, Jan
Řepková, Jana
author_facet Ištvánek, Jan
Dluhošová, Jana
Dluhoš, Petr
Pátková, Lenka
Nedělník, Jan
Řepková, Jana
author_sort Ištvánek, Jan
collection PubMed
description Red clover (Trifolium pratense) is an important forage plant worldwide. This study was directed to broadening current knowledge of red clover's coding regions and enhancing its utilization in practice by specific reanalysis of previously published assembly. A total of 42,996 genes were characterized using Illumina paired-end sequencing after manual revision of Blast2GO annotation. Genes were classified into metabolic and biosynthetic pathways in response to biological processes, with 7,517 genes being assigned to specific pathways. Moreover, 17,727 enzymatic nodes in all pathways were described. We identified 6,749 potential microsatellite loci in red clover coding sequences, and we characterized 4,005 potential simple sequence repeat (SSR) markers as generating polymerase chain reaction products preferentially within 100–350 bp. Marker density of 1 SSR marker per 12.39 kbp was achieved. Aligning reads against predicted coding sequences resulted in the identification of 343,027 single nucleotide polymorphism (SNP) markers, providing marker density of one SNP marker per 144.6 bp. Altogether, 95 SSRs in coding sequences were analyzed for 50 red clover varieties and a collection of 22 highly polymorphic SSRs with pooled polymorphism information content >0.9 was generated, thus obtaining primer pairs for application to diversity studies in T. pratense. A set of 8,623 genome-wide distributed SNPs was developed and used for polymorphism evaluation in individual plants. The polymorphic information content ranged from 0 to 0.375. Temperature switch PCR was successfully used in single-marker SNP genotyping for targeted coding sequences and for heterozygosity or homozygosity confirmation in validated five loci. Predicted large sets of SSRs and SNPs throughout the genome are key to rapidly implementing genome-based breeding approaches, for identifying genes underlying key traits, and for genome-wide association studies. Detailed knowledge of genetic relationships among breeding material can also be useful for breeders in planning crosses or for plant variety protection. Single-marker assays are useful for diagnostic applications.
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spelling pubmed-53607562017-04-05 Gene Classification and Mining of Molecular Markers Useful in Red Clover (Trifolium pratense) Breeding Ištvánek, Jan Dluhošová, Jana Dluhoš, Petr Pátková, Lenka Nedělník, Jan Řepková, Jana Front Plant Sci Plant Science Red clover (Trifolium pratense) is an important forage plant worldwide. This study was directed to broadening current knowledge of red clover's coding regions and enhancing its utilization in practice by specific reanalysis of previously published assembly. A total of 42,996 genes were characterized using Illumina paired-end sequencing after manual revision of Blast2GO annotation. Genes were classified into metabolic and biosynthetic pathways in response to biological processes, with 7,517 genes being assigned to specific pathways. Moreover, 17,727 enzymatic nodes in all pathways were described. We identified 6,749 potential microsatellite loci in red clover coding sequences, and we characterized 4,005 potential simple sequence repeat (SSR) markers as generating polymerase chain reaction products preferentially within 100–350 bp. Marker density of 1 SSR marker per 12.39 kbp was achieved. Aligning reads against predicted coding sequences resulted in the identification of 343,027 single nucleotide polymorphism (SNP) markers, providing marker density of one SNP marker per 144.6 bp. Altogether, 95 SSRs in coding sequences were analyzed for 50 red clover varieties and a collection of 22 highly polymorphic SSRs with pooled polymorphism information content >0.9 was generated, thus obtaining primer pairs for application to diversity studies in T. pratense. A set of 8,623 genome-wide distributed SNPs was developed and used for polymorphism evaluation in individual plants. The polymorphic information content ranged from 0 to 0.375. Temperature switch PCR was successfully used in single-marker SNP genotyping for targeted coding sequences and for heterozygosity or homozygosity confirmation in validated five loci. Predicted large sets of SSRs and SNPs throughout the genome are key to rapidly implementing genome-based breeding approaches, for identifying genes underlying key traits, and for genome-wide association studies. Detailed knowledge of genetic relationships among breeding material can also be useful for breeders in planning crosses or for plant variety protection. Single-marker assays are useful for diagnostic applications. Frontiers Media S.A. 2017-03-22 /pmc/articles/PMC5360756/ /pubmed/28382043 http://dx.doi.org/10.3389/fpls.2017.00367 Text en Copyright © 2017 Ištvánek, Dluhošová, Dluhoš, Pátková, Nedělník and Řepková. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Ištvánek, Jan
Dluhošová, Jana
Dluhoš, Petr
Pátková, Lenka
Nedělník, Jan
Řepková, Jana
Gene Classification and Mining of Molecular Markers Useful in Red Clover (Trifolium pratense) Breeding
title Gene Classification and Mining of Molecular Markers Useful in Red Clover (Trifolium pratense) Breeding
title_full Gene Classification and Mining of Molecular Markers Useful in Red Clover (Trifolium pratense) Breeding
title_fullStr Gene Classification and Mining of Molecular Markers Useful in Red Clover (Trifolium pratense) Breeding
title_full_unstemmed Gene Classification and Mining of Molecular Markers Useful in Red Clover (Trifolium pratense) Breeding
title_short Gene Classification and Mining of Molecular Markers Useful in Red Clover (Trifolium pratense) Breeding
title_sort gene classification and mining of molecular markers useful in red clover (trifolium pratense) breeding
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360756/
https://www.ncbi.nlm.nih.gov/pubmed/28382043
http://dx.doi.org/10.3389/fpls.2017.00367
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