Technau Gerhard Martin
Institut für Entwicklungsphysiologie der Universität zu Köln, Gyrhofstraße 17, D-5000, Köln 41, Germany.
Rouxs Arch Dev Biol. 1986 Aug;195(6):389-398. doi: 10.1007/BF00402872.
A method is presented which allows the study of the progeny of single cells during Drosophila embryogenesis. Cells from various larval anlagen of donor embryos labelled with a lineage tracer are individually transplanted from defined positions into similar, or different, positions in unlabelled hosts. The clones produced by these cells can be seen in whole mounts or in sections of fixed material, when using a histochemical marker (i.e. HRP), and/or in living embryos, when using fluorescent lineage tracers. The characteristics of the clones disclose lineage parameters, such as division patterns, morphogenetic movements and differentiation. The method is especially useful for testing the respective roles of positional information and cell lineage on the commitment of progenitor cells by transplanting these cells into heterotopic positions or into hosts of different genotypes.
本文介绍了一种方法,该方法可用于研究果蝇胚胎发育过程中单个细胞的后代。用谱系示踪剂标记的供体胚胎的各种幼虫原基中的细胞,从特定位置被逐个移植到未标记宿主的相似或不同位置。当使用组织化学标记物(即辣根过氧化物酶)时,这些细胞产生的克隆可以在固定材料的整体标本或切片中看到,而当使用荧光谱系示踪剂时,则可以在活胚胎中看到。克隆的特征揭示了谱系参数,如分裂模式、形态发生运动和分化。通过将这些细胞移植到异位位置或不同基因型的宿主中,该方法对于测试位置信息和细胞谱系在祖细胞定型中的各自作用特别有用。