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. 2012 Jul;191(3):655–669. doi: 10.1534/genetics.112.141812

Figure 1 .

Figure 1 

Photomicrographs showing wild-type and lin-12/Notch mutant phenotypes. (Left) Drosophila embryos. Neuroblasts are marked by anti-Hunchback staining, and insets show the results of staining with an antibody to the intracellular domain of Notch. (Top Left) A wild-type embryo showing the normal pattern of neuroblast segregation from the ventral ectoderm and Notch protein predominantly at the surface of ectodermal cells. (Middle Left) An embryo expressing Notchintra protein ubiquitously under heat-shock control: all ventral ectodermal cells remain ectodermal, and Notchintra protein accumulates predominantly in nuclei. (Bottom Left) A Notch embryo: all ventral ectodermal cells segregate as neuroblasts, the classic “neurogenic phenotype.” (Right) C. elegans hermaphrodite gonads. Green fluorescent protein marks the anchor cell (AC) in a wild-type hermaphrodite, two ACs in a lin-12(0) hermaphrodite, and the lack of an AC in a lin-12(d) hermaphrodite. Drosophila photomicrographs courtesy of Gary Struhl; C. elegans photomicrographs courtesy of Maria Sallee.