Kwon Moonhyuk, Hodgins Connor L, Haslam Tegan M, Roth Susan A, Nguyen Trinh-Don, Yeung Edward C, Ro Dae-Kyun
Department of Biological Sciences, University of Calgary, Calgary, AL T2N 1N4, Canada.
Division of Applied Life Sciences (BK21 Plus), Plant Molecular Biology and Biotechnology Research Center, Gyeongsang National University, Jinju 660-701, Korea.
Plants (Basel). 2022 Apr 28;11(9):1192. doi: 10.3390/plants11091192.
Sesquiterpene lactone (STL) and natural rubber (NR) are characteristic isoprenoids in lettuce (). Both STL and NR co-accumulate in laticifers, pipe-like structures located along the vasculature. NR-biosynthetic genes are exclusively expressed in laticifers, but cell-type specific expression of STL-biosynthetic genes has not been studied. Here, we examined the expression pattern of germacrene A synthase (), which catalyzes the first step in STL biosynthesis in lettuce. Quantitative PCR and Illumina read mapping revealed that the transcripts of two isoforms (/) are expressed two orders of magnitude (~100-200) higher in stems than laticifers. This result implies that the cellular site for / expression is not in laticifers. To gain more insights, promoters of / were cloned and fused to β-glucuronidase (), followed by transformations of lettuce with these promoter- constructs. In in situ GUS assays, the expression driven by the promoters was tightly associated with vascular bundles. High-resolution microsections showed that GUS signals are not present in laticifers but are detected in the vascular parenchyma cells neighboring the laticifers. These results suggest that expression of occurs in the parenchyma cells neighboring laticifers, while the resulting STL metabolites accumulate in laticifers. It can be inferred that active metabolite-trafficking occurs from the parenchyma cells to laticifers in lettuce.
倍半萜内酯(STL)和天然橡胶(NR)是生菜中的特征性类异戊二烯。STL和NR在乳管中共同积累,乳管是沿维管束分布的管状结构。NR生物合成基因仅在乳管中表达,但STL生物合成基因的细胞类型特异性表达尚未得到研究。在这里,我们研究了法呢烯A合酶()的表达模式,该酶催化生菜中STL生物合成的第一步。定量PCR和Illumina读数定位显示,两种异构体(/)的转录本在茎中的表达比在乳管中的高两个数量级(约100 - 200)。这一结果表明/的表达细胞位点不在乳管中。为了获得更多见解,克隆了/的启动子并将其与β - 葡萄糖醛酸酶()融合,然后用这些启动子构建体转化生菜。在原位GUS分析中,由启动子驱动的表达与维管束紧密相关。高分辨率切片显示,GUS信号不在乳管中出现,而是在与乳管相邻的维管薄壁细胞中检测到。这些结果表明,的表达发生在与乳管相邻的薄壁细胞中,而产生的STL代谢产物在乳管中积累。可以推断,生菜中存在从薄壁细胞到乳管的活跃代谢物运输。