Gene Classification and Mining of Molecular Markers Useful in Red Clover (Trifolium pratense) Breeding
Autor: | Jan Ištvánek, Jana Dluhošová, Lenka Pátková, Jana Řepková, Jan Nedělník, Petr Dluhoš |
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Rok vydání: | 2017 |
Předmět: |
2. Zero hunger
0106 biological sciences 0301 basic medicine Genetics Genetic diversity SNP food and beverages Single-nucleotide polymorphism genetic diversity sequencing Plant Science Biology SSR 01 natural sciences Genome SNP genotyping 03 medical and health sciences specific genes 030104 developmental biology biosynthetic pathways Genetic marker Microsatellite Gene Blast2GO 010606 plant biology & botany |
Zdroj: | Frontiers in Plant Science. 8 |
ISSN: | 1664-462X |
DOI: | 10.3389/fpls.2017.00367 |
Popis: | 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 to 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. |
Databáze: | OpenAIRE |
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