Lee Patricia N, McFall-Ngai Margaret J, Callaerts Patrick, de Couet H Gert
Department of Zoology, University of Hawaii at Manoa, Honolulu, HI 96822, USA.
Cold Spring Harb Protoc. 2009 Nov;2009(11):pdb.prot5322. doi: 10.1101/pdb.prot5322.
Whole-mount in situ hybridization is a technique used to localize and visualize specific gene transcripts in whole embryos by hybridizing labeled RNA probes complementary to the sequence of interest. A digoxigenin (DIG)-labeled riboprobe synthesized during in vitro transcription through the incorporation of DIG-labeled UTP is hybridized to the target sequence under stringent conditions, and excess unhybridized probe is removed during a series of washes. The location of the labeled riboprobe, and thus the mRNA sequence of interest, is then visualized by immunohistochemistry. This protocol outlines the steps involved in preparing Hawaiian bobtail squid (Euprymna scolopes) embryos, hybridizing a DIG-labeled riboprobe in whole-mount embryos, and visualizing the labeled RNA colorimetrically using an alkaline-phosphatase-conjugated anti-DIG antibody.
全胚胎原位杂交是一种通过将与目标序列互补的标记RNA探针进行杂交,来定位和可视化全胚胎中特定基因转录本的技术。通过掺入地高辛(DIG)标记的尿苷三磷酸(UTP)在体外转录过程中合成的地高辛(DIG)标记的核糖探针,在严格条件下与目标序列杂交,并且在一系列洗涤过程中去除过量未杂交的探针。然后通过免疫组织化学来可视化标记的核糖探针的位置,从而确定感兴趣的mRNA序列的位置。本方案概述了制备夏威夷短尾乌贼(Euprymna scolopes)胚胎、在全胚胎中杂交DIG标记的核糖探针以及使用碱性磷酸酶偶联的抗DIG抗体以比色法可视化标记RNA的步骤。