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Acta Horticulturae Sinica ›› 2024, Vol. 51 ›› Issue (1): 77-90.doi: 10.16420/j.issn.0513-353x.2023-0105

• Genetic & Breeding·Germplasm Resources·Molecular Biology • Previous Articles     Next Articles

Mining of Genetic Locus of Phenylethyl Alcohol Primrose Glycoside Abundance in Tea Plants

ZHANG Lilan, YANG Jun, WANG Rangjian*()   

  1. Fujian Branch,National Center for Tea Improvement,Tea Research Institute,Fujian Academy of Agricultural Science,Fuzhou 350013,China
  • Received:2023-08-28 Revised:2023-12-01 Online:2024-01-25 Published:2024-01-16
  • Contact: (E-mail:rangjian.wang@163.com

Abstract:

In this study,169 tea germplasms were used as the association population,and 675 245 high-quality SNP markers developed based on the simplified genome sequencing technology were used to perform genome-wide association study(GWAS)on the content of phenylethanol primrose glycosides in tea shoots from 2018 to 2020. The results demonstrated that the variation coefficient of phenylethanol primrose glycoside content among tea germplasms in different years was 61.50%-62.09%,the correlation coefficient was 0.95-0.98(P < 0.01),and the generalized heritability was 67.49%. Three GWAS analysis models detected a total of 24 stable sites(P < 0.001)which significantly associated with phenylethanol primrose glycosides in tea plants,explaining phenotypic variation rates ranging from 0.01% to 10.63%. Thirty-six excellent germplasm with excellent allelic variations at 24 major loci were identified and significantly increased phenylethanol primrose glycoside content by allelic effect analysis. A total of 10 candidate genes related to phenylethanol primrose glycoside content were preliminarily screened,namely TEA020086.1TEA003248.1TEA013029.1TEA021435.1TEA016196.1TEA029411.1TEA014564.1TEA014567.1TEA014571.1,and TEA014573.1,mainly involving secondary metabolism and transcrip- tional regulation molecular processes.

Key words: Camellia sinensis, phenylethyl alcohol primrose glycoside, genome-wide association study, candidate gene, elite allele