Matches in SemOpenAlex for { <https://semopenalex.org/work/W2897428816> ?p ?o ?g. }
- W2897428816 abstract "Tea is the most popular nonalcoholic beverage worldwide for its pleasant characteristics and healthful properties. Catechins, theanine and caffeine are the major natural products in tea buds and leaves that determine tea qualities such as infusion colors, tastes and fragrances, as well as their health benefits. Shading is a traditional and effective practice to modify natural product accumulation and to enhance the tea quality in tea plantation. However, the mechanism underlying the shading effects is not fully understood. This study aims to explore the regulation of flavonoid biosynthesis in Camellia sinensis under shading by using both metabolomic and transcriptional analyses.While shading enhanced chlorophyll accumulation, major catechins, including C, EC, GC and EGC, decreased significantly in tea buds throughout the whole shading period. The reduction of catechins and flavonols were consistent with the simultaneous down-regulation of biosynthetic genes and TFs associated with flavonoid biosynthesis. Of 16 genes involved in the flavonoid biosynthetic pathway, F3'H and FLS significantly decreased throughout shading while the others (PAL, CHSs, DFR, ANS, ANR and LAR, etc.) temporally decreased in early or late shading stages. Gene co-expression cluster analysis suggested that a number of photoreceptors and potential genes involved in UV-B signal transductions (UVR8_L, HY5, COP1 and RUP1/2) showed decreasing expression patterns consistent with structural genes (F3'H, FLS, ANS, ANR, LAR, DFR and CHSs) and potential TFs (MYB4, MYB12, MYB14 and MYB111) involved in flavonoid biosynthesis, when compared with genes in the UV-A/blue and red/far-red light signal transductions. The KEGG enrichment and matrix correlation analyses also attributed the regulation of catechin biosynthesis to the UVR8-mediated signal transduction pathway. Further UV-B treatment in the controlled environment confirmed UV-B induction on flavonols and EGCG accumulation in tea leaves.We proposed that catechin biosynthesis in C. sinensis leaves is predominantly regulated by UV through the UVR8-mediated signal transduction pathway to MYB12/MYB4 downstream effectors, to modulate flavonoid accumulation. Our study provides new insights into our understanding of regulatory mechanisms for shading-enhanced tea quality." @default.
- W2897428816 created "2018-10-26" @default.
- W2897428816 creator A5007855424 @default.
- W2897428816 creator A5026180045 @default.
- W2897428816 creator A5026323967 @default.
- W2897428816 creator A5029488879 @default.
- W2897428816 creator A5057035600 @default.
- W2897428816 creator A5071909250 @default.
- W2897428816 creator A5079286679 @default.
- W2897428816 creator A5083909930 @default.
- W2897428816 date "2018-10-12" @default.
- W2897428816 modified "2023-10-12" @default.
- W2897428816 title "Metabolite profiling and transcriptomic analyses reveal an essential role of UVR8-mediated signal transduction pathway in regulating flavonoid biosynthesis in tea plants (Camellia sinensis) in response to shading" @default.
- W2897428816 cites W160494749 @default.
- W2897428816 cites W1837288435 @default.
- W2897428816 cites W1868987770 @default.
- W2897428816 cites W1936666270 @default.
- W2897428816 cites W1944597845 @default.
- W2897428816 cites W1963670602 @default.
- W2897428816 cites W1963944394 @default.
- W2897428816 cites W1965514968 @default.
- W2897428816 cites W1971706091 @default.
- W2897428816 cites W1971792941 @default.
- W2897428816 cites W1978404628 @default.
- W2897428816 cites W1984921996 @default.
- W2897428816 cites W1985298763 @default.
- W2897428816 cites W1986463052 @default.
- W2897428816 cites W1989750273 @default.
- W2897428816 cites W1993394922 @default.
- W2897428816 cites W1998587460 @default.
- W2897428816 cites W2005925816 @default.
- W2897428816 cites W2009149233 @default.
- W2897428816 cites W2018260893 @default.
- W2897428816 cites W2021943076 @default.
- W2897428816 cites W2037876340 @default.
- W2897428816 cites W2046064827 @default.
- W2897428816 cites W2048588293 @default.
- W2897428816 cites W2059568988 @default.
- W2897428816 cites W2061119080 @default.
- W2897428816 cites W2063705471 @default.
- W2897428816 cites W2071809726 @default.
- W2897428816 cites W2073766890 @default.
- W2897428816 cites W2081050496 @default.
- W2897428816 cites W2084150082 @default.
- W2897428816 cites W2089764712 @default.
- W2897428816 cites W2094745283 @default.
- W2897428816 cites W2106444597 @default.
- W2897428816 cites W2114057457 @default.
- W2897428816 cites W2117719962 @default.
- W2897428816 cites W2121777152 @default.
- W2897428816 cites W2126419817 @default.
- W2897428816 cites W2131774142 @default.
- W2897428816 cites W2132991478 @default.
- W2897428816 cites W2134281770 @default.
- W2897428816 cites W2134805337 @default.
- W2897428816 cites W2135959854 @default.
- W2897428816 cites W2158330403 @default.
- W2897428816 cites W2165402269 @default.
- W2897428816 cites W2166563780 @default.
- W2897428816 cites W2170377424 @default.
- W2897428816 cites W2172072250 @default.
- W2897428816 cites W2294821411 @default.
- W2897428816 cites W2315670822 @default.
- W2897428816 cites W2327619244 @default.
- W2897428816 cites W2337691416 @default.
- W2897428816 cites W2514015068 @default.
- W2897428816 cites W2590523881 @default.
- W2897428816 cites W2600985089 @default.
- W2897428816 cites W2607191033 @default.
- W2897428816 cites W2610308012 @default.
- W2897428816 cites W2619015919 @default.
- W2897428816 cites W2624827669 @default.
- W2897428816 cites W2734861113 @default.
- W2897428816 cites W2762064049 @default.
- W2897428816 cites W2783129650 @default.
- W2897428816 cites W2783605644 @default.
- W2897428816 cites W2794671147 @default.
- W2897428816 cites W2800563766 @default.
- W2897428816 cites W2885529396 @default.
- W2897428816 cites W2949206574 @default.
- W2897428816 cites W88956824 @default.
- W2897428816 doi "https://doi.org/10.1186/s12870-018-1440-0" @default.
- W2897428816 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6186127" @default.
- W2897428816 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30314466" @default.
- W2897428816 hasPublicationYear "2018" @default.
- W2897428816 type Work @default.
- W2897428816 sameAs 2897428816 @default.
- W2897428816 citedByCount "74" @default.
- W2897428816 countsByYear W28974288162018 @default.
- W2897428816 countsByYear W28974288162019 @default.
- W2897428816 countsByYear W28974288162020 @default.
- W2897428816 countsByYear W28974288162021 @default.
- W2897428816 countsByYear W28974288162022 @default.
- W2897428816 countsByYear W28974288162023 @default.
- W2897428816 crossrefType "journal-article" @default.
- W2897428816 hasAuthorship W2897428816A5007855424 @default.
- W2897428816 hasAuthorship W2897428816A5026180045 @default.
- W2897428816 hasAuthorship W2897428816A5026323967 @default.
- W2897428816 hasAuthorship W2897428816A5029488879 @default.
- W2897428816 hasAuthorship W2897428816A5057035600 @default.