Molecular regulation of catechins biosynthesis in tea [Camellia sinensis (L.) O. Kuntze]
Catechins are bioprospecting molecules present in tea and any effort towards metabolic engineering of this important moiety would require knowledge on gene regulation. These are synthesized through the activities of phenylpropanoid and flavonoid pathways. Expression regulation of various genes of th...
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Veröffentlicht in: | Gene 2012-03, Vol.495 (2), p.205-210 |
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Sprache: | eng |
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Zusammenfassung: | Catechins are bioprospecting molecules present in tea and any effort towards metabolic engineering of this important moiety would require knowledge on gene regulation. These are synthesized through the activities of phenylpropanoid and flavonoid pathways. Expression regulation of various genes of these pathways namely phenylalanine ammonia-lyase (CsPAL), cinnamate 4-hydroxylase (CsC4H), p-coumarate:CoA ligase (Cs4CL), flavanone 3-hydroxylase (CsF3H), dihydroflavonol 4-reductase (CsDFR) and anthocyanidin reductase (CsANR) was accomplished previously. In depth analyses of the remaining genes namely, chalcone synthase (CsCHS), chalcone isomerase (CsCHI), flavonoid 3′5′-hydroxylase (CsF3′5′H) and anthocyanidin synthase (CsANS) were lacking. The objective of the work was to clone and analyze these genes so as to generate a comprehensive knowledge on the critical genes of catechins biosynthesis pathway. Gene expression analysis was carried out in response to leaf age and external cues (drought stress, abscisic acid, gibberellic acid treatments and wounding). A holistic analysis suggested that CsCHI, CsF3H, CsDFR, CsANS and CsANR were amongst the critical regulatory genes in regulating catechins content.
►CHS, CHI, F3′5′H and ANS associated with catechins biosynthesis in tea were cloned. ►Catechins content and gene expression varied with tissue type and external cues. ►A comprehensive analysis on the present and earlier published data was performed. ►CHI, F3H, DFR, ANS and ANR were amongst the genes regulating catechins content. |
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ISSN: | 0378-1119 1879-0038 |
DOI: | 10.1016/j.gene.2011.12.029 |