Liu Zixi, Hu Xi, Nie Jing, Li Xiaojun, Wang Qing, Liu Wenqian, Wang Tao, Lu Xiaohong, Gao Shunli, Gao Lihong, Zhang Wenna
Beijing Key Laboratory of Growth and Developmental Regulation for Protected Vegetable Crops, China Agricultural University, Beijing 100193, China.
Plants (Basel). 2020 Oct 29;9(11):1461. doi: 10.3390/plants9111461.
Cucumber ( L.) is one of the main vegetable crops in China. The physiological cultivation mechanism and gene function characteristics of cucumber are of great significance to the construction of modern agriculture. Due to the low genetic transformation rate of cucumber, only in situ hybridization, which does not involve the progress of gene modified transformation, is convenient to study mRNA localization, so it is more suitable for determination on mRNA localization in the mature tissue of cucumber. At present, the existing in situ hybridization technology system is more suitable for cucumber meristem than for the mature tissue of cucumber seedlings. Therefore, we optimized the traditional plant in situ hybridization protocol. Taking a known gene CsNPF7.2 (Nitrate Transporter Families protein) as an example, we then optimized the steps of plant tissue culture, gene probe preparation, plant material sampling and fixation, preparation of cross section, hybridization pretreatment, hybridization incubation, chromogenic reaction, microscopy examination, and treatment after reaction termination in order to obtain a new RNA in situ hybridization technique suitable for identification on mRNA localization in mature tissues of cucumber seedlings. This optimized technique will ensure the yield of probes, the integrity of RNA molecules, and the clarity and integrity of plant tissue structure, which is conducive to the study of gene function and screening of key genes in cucumber.
黄瓜(Cucumis sativus L.)是中国主要蔬菜作物之一。黄瓜的生理栽培机制和基因功能特性对现代农业建设具有重要意义。由于黄瓜的遗传转化率较低,仅原位杂交不涉及基因修饰转化过程,便于研究mRNA定位,因此更适合用于黄瓜成熟组织中mRNA定位的测定。目前,现有的原位杂交技术体系对黄瓜分生组织的适用性优于黄瓜幼苗的成熟组织。因此,我们优化了传统的植物原位杂交方案。以已知基因CsNPF7.2(硝酸盐转运蛋白家族蛋白)为例,我们随后对植物组织培养、基因探针制备、植物材料取样与固定、切片制备、杂交预处理、杂交孵育、显色反应、显微镜检查以及反应终止后的处理等步骤进行了优化,以获得一种适用于鉴定黄瓜幼苗成熟组织中mRNA定位的新型RNA原位杂交技术。这种优化后的技术将确保探针产量、RNA分子的完整性以及植物组织结构的清晰度和完整性,有利于黄瓜基因功能的研究和关键基因的筛选。