Palapol Yossapol, Ketsa Saichol, Lin-Wang Kui, Ferguson Ian B, Allan Andrew C
Department of Horticulture, Faculty of Agriculture, Kasetsart University, Bangkok, 10900, Thailand.
Planta. 2009 May;229(6):1323-34. doi: 10.1007/s00425-009-0917-3. Epub 2009 Mar 22.
Mangosteen (Garcinia mangostana L.) fruit undergo rapid red colour development, both on the tree and after harvest, resulting in high anthocyanin production in the pericarp. Here, we report the isolation of three full-length mangosteen MYB transcription factors (GmMYB1, GmMYB7 and GmMYB10) and all the anthocyanin biosynthetic pathway genes (GmPal to GmUFGT). Phylogenetic analysis at the protein level of the R2R3-MYB transcription factor family showed GmMYB10 had a high degree of similarity with production of anthocyanin pigment1 in Arabidopsis and as well as sequences from other plant species related to the elevation of anthocyanin pigmentation. In transient transactivation assays, GmMYB10, co-expressed with AtbHLH2, strongly activated the GmDFR and AtDFR promoters. Transcripts of GmMYB10 and GmUFGT were highly abundant with onset of pigmentation and subsequently during red colouration. Our results suggest that GmMYB10 plays an important role in regulating anthocyanin biosynthesis both on the tree and after harvest, while GmUFGT may be a key biosynthetic gene in mangosteen pigmentation. The expression patterns of GmMYB10 and GmUFGT correlated with ethylene production that increased linearly until stage 5 (dark purple) and decreased thereafter. 1-Methycyclopropene (1-MCP) clearly delayed red colouration with resulting down-regulation of GmMYB10. These results suggest that the effect of ethylene on anthocyanin biosynthesis may be via the regulation of GmMYB10 expression.
山竹(Garcinia mangostana L.)果实无论是在树上还是采收后,都会迅速变红,导致果皮中产生大量花青素。在此,我们报告了三个全长山竹MYB转录因子(GmMYB1、GmMYB7和GmMYB10)以及所有花青素生物合成途径基因(从GmPal到GmUFGT)的分离。R2R3-MYB转录因子家族蛋白质水平的系统发育分析表明,GmMYB10与拟南芥中花青素色素合成1以及其他与花青素色素沉着增加相关的植物物种序列具有高度相似性。在瞬时反式激活试验中,与AtbHLH2共表达的GmMYB10强烈激活了GmDFR和AtDFR启动子。GmMYB10和GmUFGT的转录本在色素沉着开始时以及随后的红色着色过程中高度丰富。我们的结果表明,GmMYB10在调节山竹果实树上和采收后的花青素生物合成中起重要作用,而GmUFGT可能是山竹色素沉着中的关键生物合成基因。GmMYB10和GmUFGT的表达模式与乙烯产量相关,乙烯产量在第5阶段(深紫色)之前呈线性增加,此后下降。1-甲基环丙烯(1-MCP)明显延迟了红色着色,并导致GmMYB10的下调。这些结果表明,乙烯对花青素生物合成的影响可能是通过调节GmMYB10的表达来实现的。