Mishra Ajay Kumar, Kocábek Tomáš, Nath Vishnu Sukumari, Khan Ahamed, Matoušek Jaroslav, Hazzouri Khaled M, Sudalaimuthuasari Naganeeswaran, Krofta Karel, Ludwig-Müller Jutta, Amiri Khaled M A
Khalifa Centre for Genetic Engineering and Biotechnology, United Arab Emirates University, Al Ain, 15551, United Arab Emirates.
Biology Centre, Czech Academy of Sciences, Institute of Plant Molecular Biology, Branišovská 31, 370 05, České Budějovice, Czech Republic.
Plant Physiol Biochem. 2023 Apr;197:107636. doi: 10.1016/j.plaphy.2023.03.013. Epub 2023 Mar 10.
Hop (Humulus lupulus) biosynthesizes the highly economically valuable secondary metabolites, which include flavonoids, bitter acids, polyphenols and essential oils. These compounds have important pharmacological properties and are widely implicated in the brewing industry owing to bittering flavor, floral aroma and preservative activity. Our previous studies documented that ternary MYB-bHLH-WD40 (MBW) and binary WRKY1-WD40 (WW) protein complexes transcriptionally regulate the accumulation of bitter acid (BA) and prenylflavonoids (PF). In the present study, we investigated the regulatory functions of the R2R3-MYB repressor HlMYB7 transcription factor, which contains a conserved N-terminal domain along with the repressive motif EAR, in regulating the PF- and BA-biosynthetic pathway and their accumulation in hop. Constitutive expression of HlMYB7 resulted in transcriptional repression of structural genes involved in the terminal steps of biosynthesis of PF and BA, as well as stunted growth, delayed flowering, and reduced tolerance to viroid infection in hop. Furthermore, yeast two-hybrid and transient reporter assays revealed that HlMYB7 targets both PF and BA pathway genes and suppresses MBW and WW protein complexes. Heterologous expression of HlMYB7 leads to down-regulation of structural genes of flavonoid pathway in Arabidopsis thaliana, including a decrease in anthocyanin content in Nicotiana tabacum. The combined results from functional and transcriptomic analyses highlight the important role of HlMYB7 in fine-tuning and balancing the accumulation of secondary metabolites at the transcriptional level, thus offer a plausible target for metabolic engineering in hop.
啤酒花(Humulus lupulus)生物合成具有高度经济价值的次生代谢产物,其中包括黄酮类化合物、苦味酸、多酚和精油。这些化合物具有重要的药理特性,由于其苦味、花香和防腐活性,在酿造工业中广泛应用。我们之前的研究表明,三元MYB-bHLH-WD40(MBW)和二元WRKY1-WD40(WW)蛋白复合物可转录调控苦味酸(BA)和异戊烯基黄酮(PF)的积累。在本研究中,我们研究了R2R3-MYB阻遏物HlMYB7转录因子的调控功能,该转录因子包含一个保守的N端结构域以及阻遏基序EAR,其在调控PF和BA生物合成途径及其在啤酒花中的积累方面发挥作用。HlMYB7的组成型表达导致参与PF和BA生物合成末端步骤的结构基因转录受到抑制,同时啤酒花出现生长发育迟缓、开花延迟以及对类病毒感染的耐受性降低。此外,酵母双杂交和瞬时报告基因检测表明,HlMYB7靶向PF和BA途径基因,并抑制MBW和WW蛋白复合物。HlMYB7的异源表达导致拟南芥中黄酮类途径结构基因的下调,包括烟草中花青素含量的降低。功能和转录组分析的综合结果突出了HlMYB7在转录水平上微调并平衡次生代谢产物积累方面的重要作用,从而为啤酒花的代谢工程提供了一个合理的靶点。