Pires Rita Costa, Ferro Ana, Capote Tiago, Usié Ana, Correia Bárbara, Pinto Glória, Menéndez Esther, Marum Liliana
Centro de Biotecnologia Agrícola e Agro-Alimentar do Alentejo (CEBAL)/Instituto Politécnico de Beja (IPBeja), 7801-908, Beja, Portugal.
MED - Mediterranean Institute for Agriculture, Environment and Development, CEBAL - Centro de Biotecnologia Agrícola e Agro-Alimentar do Alentejo, 7801-908, Beja, Portugal.
Mol Biotechnol. 2023 Mar;65(3):419-432. doi: 10.1007/s12033-022-00542-9. Epub 2022 Aug 17.
An accurate profile of gene expression at a cellular level can contribute to a better understanding of biological processes and complexities involved in regulatory mechanism of woody plants. Laser microdissection is one technique that allows isolation of specific, target cells or tissue from a heterogeneous cell population. This technique entails microscopic visualization of the selected tissue and use a laser beam to separate the desired cells from surrounding tissue. Initial identification of these cells is made based on morphology and/or histological staining. Some works have been made in several tissues and plant models. However, there are few studies of laser microdissection application in woody species, particularly, lignified and suberized cells. Moreover, the presence of high level of suberin in cell walls can be a big challenge for the application of this approach. In our study it was developed a technique for tissue isolation, using laser microdissection of four different plant cell types (phellogen, lenticels, cortex and xylem) from woody tissues of cork oak (Quercus suber), followed by RNA extraction and RNA-Seq. We tested several methodologies regarding laser microdissection, cryostat equipments, fixation treatments, duration of single-cells collection and number of isolated cells by laser microdissection and RNA extraction procedures. A simple and efficient protocol for tissue isolation by laser microdissection and RNA purification was obtained, with a final method validation of RNA-Seq analysis. The optimized methodology combining RNA-Seq for expression analysis will contribute to elucidate the molecular pathways associated with different development processes of the xylem and phellem in oaks, including the lenticular channels formation.
在细胞水平上准确描绘基因表达情况,有助于更好地理解木本植物调控机制中涉及的生物学过程和复杂性。激光显微切割是一种能够从异质细胞群体中分离特定目标细胞或组织的技术。该技术需要对选定的组织进行显微镜观察,并使用激光束将所需细胞与周围组织分离。这些细胞的初步识别基于形态学和/或组织学染色。在几种组织和植物模型方面已经开展了一些工作。然而,在木本物种,特别是木质化和栓质化细胞中,激光显微切割应用的研究较少。此外,细胞壁中高水平栓质的存在可能是该方法应用的一大挑战。在我们的研究中,开发了一种组织分离技术,使用激光显微切割从栓皮栎(Quercus suber)的木质组织中分离四种不同的植物细胞类型(木栓形成层、皮孔、皮层和木质部),随后进行RNA提取和RNA测序。我们测试了有关激光显微切割、低温恒温器设备、固定处理、单细胞收集持续时间以及通过激光显微切割分离的细胞数量和RNA提取程序的几种方法。获得了一种通过激光显微切割进行组织分离和RNA纯化的简单高效方案,并对RNA测序分析进行了最终方法验证。将RNA测序与表达分析相结合的优化方法,将有助于阐明与橡树木质部和周皮不同发育过程相关的分子途径,包括皮孔通道的形成。