SNP markers found in non-coding regions can distinguish among low-variant genotypes of Arabica and other coffee species

Development of efficient and scalable methods for molecular identification of Coffea spp. are necessary to accelerate studies related to the characterization of germplasm for both conservation or breeding purposes, and the validation of coffee germplasm. The low genetic diversity of coffee hinders t...

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Published inGenetic resources and crop evolution Vol. 70; no. 4; pp. 1215 - 1228
Main Authors Bolívar-González, Alejandro, Molina-Bravo, Ramón, Solano-Sánchez, William, Araya-Valverde, Emanuel, Ivamoto-Suzuki, Suzana T., Pereira, Luiz F. P., Gatica-Arias, Andrés
Format Journal Article
LanguageEnglish
Published Dordrecht Springer Netherlands 01.04.2023
Springer Nature B.V
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Abstract Development of efficient and scalable methods for molecular identification of Coffea spp. are necessary to accelerate studies related to the characterization of germplasm for both conservation or breeding purposes, and the validation of coffee germplasm. The low genetic diversity of coffee hinders the establishment of protocols that facilitate the molecular characterization of a given genotype. In this study, nucleotide variability was analyzed at 22 loci in the genome of 19 coffee accessions using de novo primer sets and high-resolution melting (HRM). Single nucleotide polymorphisms (SNPs) variants were studied in coding regions of genes implicated in sucrose accumulation in the seed, Sucrose synthase 2 ( SUS2 ), Ent-kaurene oxidase 1 ( CaKO1) , and Caffeoyl-coenzyme A 3-O-methyltransferase ( CcOAOMT). The non-coding Internal transcribed spacer 2 ( ITS2) region was also studied. Variability was shown at 103 positions both at the interspecies level (15 loci) and among varieties of Coffea arabica L. (4 loci). The HMR technique for identification of variants in genes CaKO1 , SUS2 , CcoAOMT, as well as in the ITS2 region proved to be a robust technique for germplasm characterization. More important this technique can be used for fingerprinting and traceability of coffee grain exports which is an increasing market-consumer demand.
AbstractList Development of efficient and scalable methods for molecular identification of Coffea spp. are necessary to accelerate studies related to the characterization of germplasm for both conservation or breeding purposes, and the validation of coffee germplasm. The low genetic diversity of coffee hinders the establishment of protocols that facilitate the molecular characterization of a given genotype. In this study, nucleotide variability was analyzed at 22 loci in the genome of 19 coffee accessions using de novo primer sets and high-resolution melting (HRM). Single nucleotide polymorphisms (SNPs) variants were studied in coding regions of genes implicated in sucrose accumulation in the seed, Sucrose synthase 2 (SUS2), Ent-kaurene oxidase 1 (CaKO1), and Caffeoyl-coenzyme A 3-O-methyltransferase (CcOAOMT). The non-coding Internal transcribed spacer 2 (ITS2) region was also studied. Variability was shown at 103 positions both at the interspecies level (15 loci) and among varieties of Coffea arabica L. (4 loci). The HMR technique for identification of variants in genes CaKO1, SUS2, CcoAOMT, as well as in the ITS2 region proved to be a robust technique for germplasm characterization. More important this technique can be used for fingerprinting and traceability of coffee grain exports which is an increasing market-consumer demand.
Development of efficient and scalable methods for molecular identification of Coffea spp. are necessary to accelerate studies related to the characterization of germplasm for both conservation or breeding purposes, and the validation of coffee germplasm. The low genetic diversity of coffee hinders the establishment of protocols that facilitate the molecular characterization of a given genotype. In this study, nucleotide variability was analyzed at 22 loci in the genome of 19 coffee accessions using de novo primer sets and high-resolution melting (HRM). Single nucleotide polymorphisms (SNPs) variants were studied in coding regions of genes implicated in sucrose accumulation in the seed, Sucrose synthase 2 ( SUS2 ), Ent-kaurene oxidase 1 ( CaKO1) , and Caffeoyl-coenzyme A 3-O-methyltransferase ( CcOAOMT). The non-coding Internal transcribed spacer 2 ( ITS2) region was also studied. Variability was shown at 103 positions both at the interspecies level (15 loci) and among varieties of Coffea arabica L. (4 loci). The HMR technique for identification of variants in genes CaKO1 , SUS2 , CcoAOMT, as well as in the ITS2 region proved to be a robust technique for germplasm characterization. More important this technique can be used for fingerprinting and traceability of coffee grain exports which is an increasing market-consumer demand.
Author Araya-Valverde, Emanuel
Gatica-Arias, Andrés
Ivamoto-Suzuki, Suzana T.
Pereira, Luiz F. P.
Solano-Sánchez, William
Bolívar-González, Alejandro
Molina-Bravo, Ramón
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CitedBy_id crossref_primary_10_1016_j_bcab_2024_103095
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Keywords HRM
Single-nucleotide polymorphism
Coffee
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Snippet Development of efficient and scalable methods for molecular identification of Coffea spp. are necessary to accelerate studies related to the characterization...
Development of efficient and scalable methods for molecular identification of Coffea spp. are necessary to accelerate studies related to the characterization...
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SubjectTerms Agriculture
Biomedical and Life Sciences
Breeding
Coenzyme A
Coffea arabica
Coffee
Fingerprinting
Genes
Genetic diversity
Genomes
Genotypes
Germplasm
Life Sciences
Methyltransferase
Nucleotides
Plant Genetics and Genomics
Plant Physiology
Plant Sciences
Plant Systematics/Taxonomy/Biogeography
Research Article
Single-nucleotide polymorphism
Sucrose
Sucrose synthase
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Title SNP markers found in non-coding regions can distinguish among low-variant genotypes of Arabica and other coffee species
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