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 in | Genetic resources and crop evolution Vol. 70; no. 4; pp. 1215 - 1228 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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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Coffea
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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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