4.7 Article

Association mapping of caffeine content with TCS1 in tea plant and its related species

期刊

PLANT PHYSIOLOGY AND BIOCHEMISTRY
卷 105, 期 -, 页码 251-259

出版社

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.plaphy.2016.04.032

关键词

Caffeine; Linkage disequilibrium mapping; Single-nucleotide polymorphism; Tea caffeine synthase; Tea plant

资金

  1. Earmarked Fund for China Agriculture Research System [CARS-023]
  2. Chinese Academy of Agricultural Sciences through the Agricultural Science and Technology Innovation Program [CAASASTIP-2014-TRICAAS]
  3. National Natural Science Foundation of China [30901159, 31170624, 31100504, 31400581]
  4. National Science and Technology Support Program of China [2013BAD01B03]
  5. Science and Technology Major Project for New Crop Varieties Breeding of Zhejiang Province [2012C12905]
  6. Natural Science Foundation of Zhejiang Province [LY13C160005]

向作者/读者索取更多资源

Caffeine is the most abundant purine alkaloid in majority of tea plant and its related species. This purine alkaloid contributes to the important flavor and health attributes of tea. Tea caffeine synthase 1 (TCS1, EC 2.1.1.159/2.1.1.160) gene plays a crucial role in caffeine biosynthesis. The objective of this study was to investigate the genetic relationship between the TCS1 and caffeine content of tea plant and its related species using association mapping. We identified 87 single-nucleotide polymorphisms (SNPs, pi = 0.00447) by resequencing the TCS1 locus of 44 tea accessions. Linkage disequilibrium (LD) analysis showed that LD did not extend over the entire gene (r(2) < 0.1, within 1000 bp). Two cleaved amplified polymorphism sequence (CAPS) markers were developed from sequence variations (SNP4318 and SNP6252). By association mapping, we identified SNP4318 associated with caffeine content in four environments, explaining 4.0%-7.7% of the phenotypic variance. We also validated the significant marker-trait associations in site-directed mutagenesis experiments. Examination of allelic variation and linkage disequilibrium by a candidate-gene-based approach can help to decipher the genetic basis of caffeine biosynthesis. Moreover, the SNP marker identified in this study can potentially be applied for future marker-assisted selection to improve tea quality. (C) 2016 Elsevier Masson SAS. All rights reserved.

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