Yamaguchi Tomoko, Kurihara Yukio, Makita Yuko, Okubo-Kurihara Emiko, Kageyama Ami, Osada Emi, Shimada Setsuko, Tsuchida Hiroko, Shimada Hiroaki, Matsui Minami
Synthetic Genomics Research Group, RIKEN Center for Sustainable Resource Science, Yokohama, Kanagawa 230-0045, Japan.
Department of Biological Science and Technology, Tokyo University of Science, Katsushika, Tokyo 125-8585, Japan.
Plants (Basel). 2020 May 26;9(6):674. doi: 10.3390/plants9060674.
Natural rubber is the main component of latex obtained from laticifer cells of . For improving rubber yield, it is essential to understand the genetic molecular mechanisms responsible for laticifer differentiation and rubber biosynthesis. Jasmonate enhances both secondary laticifer differentiation and rubber biosynthesis. Here, we carried out time-course RNA-seq analysis in suspension-cultured cells treated with methyljasmonic acid (MeJA) to characterize the gene expression profile. Gene Ontology (GO) analysis showed that the term "cell differentiation" was enriched in upregulated genes at 24 hours after treatment, but inversely, the term was enriched in downregulated genes at 5 days, indicating that MeJA could induce cell differentiation at an early stage of the response. Jasmonate signaling is activated by MYC2, a basic helix-loop-helix (bHLH)-type transcription factor (TF). The aim of this work was to find any links between transcriptomic changes after MeJA application and regulation by TFs. Using an in vitro binding assay, we traced candidate genes throughout the whole genome that were targeted by four bHLH TFs: Hb_MYC2-1, Hb_MYC2-2, Hb_bHLH1, and Hb_bHLH2. The latter two are highly expressed in laticifer cells. Their physical binding sites were found in the promoter regions of a variety of other TF genes, which are differentially expressed upon MeJA exposure, and rubber biogenesis-related genes including and . These studies suggest the possibilities that and regulate cell differentiation and that and promote rubber biosynthesis. We expect that our findings will help to increase natural rubber yield through genetic control in the future.
天然橡胶是从 的乳管细胞中获得的乳胶的主要成分。为了提高橡胶产量,了解负责乳管分化和橡胶生物合成的遗传分子机制至关重要。茉莉酸酯可增强次生乳管分化和橡胶生物合成。在此,我们对用茉莉酸甲酯(MeJA)处理的悬浮培养细胞进行了时间进程RNA测序分析,以表征基因表达谱。基因本体论(GO)分析表明,“细胞分化”这一术语在处理后24小时的上调基因中富集,但相反,该术语在5天时在下调基因中富集,这表明MeJA可在反应的早期阶段诱导细胞分化。茉莉酸信号由MYC2激活,MYC2是一种基本的螺旋-环-螺旋(bHLH)型转录因子(TF)。这项工作的目的是寻找MeJA应用后转录组变化与TF调控之间的任何联系。使用体外结合试验,我们在整个基因组中追踪了四个bHLH TF(Hb_MYC2-1、Hb_MYC2-2、Hb_bHLH1和Hb_bHLH2)靶向的候选基因。后两个在乳管细胞中高度表达。它们的物理结合位点存在于多种其他TF基因的启动子区域,这些基因在MeJA暴露后差异表达,以及包括 和 在内的橡胶生物合成相关基因。这些研究表明 和 调节细胞分化以及 和 促进橡胶生物合成的可能性。我们期望我们的发现将有助于未来通过基因控制提高天然橡胶产量。