Department of Plant Sciences, University of Cambridge, Downing Street, Cambridge, CB2 3EA, UK.
Plant J. 2023 Oct;116(2):604-628. doi: 10.1111/tpj.16394. Epub 2023 Aug 15.
A combination of streamlined genetics, experimental tractability and relative morphological simplicity compared to vascular plants makes the liverwort Marchantia polymorpha an ideal model system for studying many aspects of plant biology. Here we describe a transformation vector combining a constitutive fluorescent membrane marker with a nuclear marker that is regulated by nearby enhancer elements and use this to produce a library of enhancer trap lines for Marchantia. Screening gemmae from these lines allowed the identification and characterization of novel marker lines, including markers for rhizoids and oil cells. The library allowed the identification of a margin tissue running around the thallus edge, highlighted during thallus development. The expression of this marker is correlated with auxin levels. We generated multiple markers for the meristematic apical notch region, which have different spatial expression patterns, reappear at different times during meristem regeneration following apical notch excision and have varying responses to auxin supplementation or inhibition. This reveals that there are proximodistal substructures within the apical notch that could not be observed otherwise. We employed our markers to study Marchantia sporeling development, observing meristem emergence as defining the protonema-to-prothallus stage transition, and subsequent production of margin tissue during the prothallus stage. Exogenous auxin treatment stalls meristem emergence at the protonema stage but does not inhibit cell division, resulting in callus-like sporelings with many rhizoids, whereas pharmacologically inhibiting auxin synthesis and transport does not prevent meristem emergence. This enhancer trap system presents a useful resource for the community and will contribute to future Marchantia research.
与维管植物相比,简化的遗传学、实验可操作性和相对形态简单性的结合,使地钱(Marchantia polymorpha)成为研究植物生物学许多方面的理想模式系统。在这里,我们描述了一个转化载体,该载体将组成型荧光膜标记物与受附近增强子元件调控的核标记物结合,并利用该载体构建了地钱的增强子捕获系文库。筛选这些系的原丝体允许鉴定和表征新的标记系,包括根状丝和油细胞的标记物。该文库允许鉴定沿叶状体边缘运行的边缘组织,在叶状体发育过程中该组织会突出显示。该标记物的表达与生长素水平相关。我们为分生组织顶端切迹区域生成了多个标记物,它们具有不同的空间表达模式,在顶端切迹切除后再生分生组织期间以不同的时间重新出现,并且对生长素补充或抑制有不同的反应。这表明在顶端切迹区域内存在近-远侧亚结构,否则无法观察到。我们利用我们的标记物研究地钱孢子体发育,观察到分生组织的出现定义了原丝体到叶状体阶段的过渡,随后在叶状体阶段产生边缘组织。外源生长素处理在原丝体阶段阻止分生组织的出现,但不会抑制细胞分裂,导致具有许多根状丝的愈伤组织样孢子体,而药理学抑制生长素的合成和运输并不能阻止分生组织的出现。该增强子捕获系统为社区提供了一个有用的资源,并将有助于未来的地钱研究。