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.prot5321. doi: 10.1101/pdb.prot5321.
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 a 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 techniques for preparing RNA probes for whole-mount in situ hybridization in Hawaiian bobtail squid (Euprymna scolopes) embryos from linearized plasmid DNA or polymerase chain reaction (PCR) products.
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,在严格条件下与靶序列杂交,在一系列洗涤过程中去除过量的未杂交探针。然后通过免疫组织化学观察标记核糖探针的位置,从而观察到感兴趣的mRNA序列。本方案概述了从线性化质粒DNA或聚合酶链反应(PCR)产物制备用于夏威夷短尾鱿鱼(Euprymna scolopes)胚胎全胚胎原位杂交的RNA探针的技术。