Yochem J, Gu T, Han M
Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, Colorado 80309, USA.
Genetics. 1998 Jul;149(3):1323-34. doi: 10.1093/genetics/149.3.1323.
A fusion of the sur-5 protein to the green fluorescent protein containing a nuclear localization signal is demonstrated as a marker for genetic mosaic analysis in the nematode Caenorhabditis elegans. Because of an extensive accumulation of bright fluorescence in many nuclei, normal growth plates, each containing hundreds of worms, can be rapidly screened with a dissecting microscope for rare mosaic individuals. As the marker can also be used to detect transgenic worms, the construction of strains for mosaic analyses can be minimized. In the course of examining rare mosaic animals, an unexpected pattern of fluorescence was noticed for hyp6, a syncytial component of the hypodermis, which indicated that the marker may serve as a means of assessing cellular fusions during development. Immunofluorescent staining of adherens junctions confirmed a postembryonic fusion of hyp6 with hyp7, the major syncytium of the hypodermis.
在秀丽隐杆线虫中,将含有核定位信号的绿色荧光蛋白与sur-5蛋白融合,被证明是一种用于遗传镶嵌分析的标记。由于许多细胞核中大量积累了明亮的荧光,因此可以使用解剖显微镜快速筛选正常生长平板(每个平板包含数百条蠕虫)以寻找罕见的镶嵌个体。由于该标记还可用于检测转基因蠕虫,因此可以最大限度地减少用于镶嵌分析的菌株构建。在检查罕见的镶嵌动物过程中,发现了皮下组织的一个合胞体成分hyp6出现了意外的荧光模式,这表明该标记可能是评估发育过程中细胞融合的一种手段。黏着连接的免疫荧光染色证实了hyp6与皮下组织的主要合胞体hyp7在胚胎后期发生了融合。