Chow K L, Hall D H, Emmons S W
Department of Molecular Genetics, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Development. 1995 Nov;121(11):3615-26. doi: 10.1242/dev.121.11.3615.
The gene mab-21, which encodes a novel protein of 386 amino acids, is required for the choice of alternate cell fates by several cells in the C. elegans male tail. Three cells descended from the ray 6 precursor cell adopt fates of anterior homologs, and a fourth, lineally unrelated hypodermal cell is transformed into a neuroblast. The affected cells lie together in the lateral tail epidermis, suggesting that mab-21 acts as part of a short-range pattern-formation mechanism. Each of the changes in cell fate brought about by mab-21 mutants can be interpreted as a posterior-to-anterior homeotic transformation. mab-21 mutant males and hermaphrodites have additional pleiotropic phenotypes affecting movement, body shape and fecundity, indicating that mab-21 has functions outside the tail region of males. We show that the three known alleles of mab-21 are hypomorphs of a new gene. Mosaic analysis revealed that mab-21 acts cell autonomously to specify the properties of the sensory ray, but non-autonomously in the hypodermal versus neuroblast cell fate choice. Presence of cell signalling in the choice of the neuroblast fate was confirmed by cell ablation experiments. Mutations in mab-21 were shown previously to be genetic modifiers of the effects of HOM-C/Hox gene mutations on ray identity specification. The results presented here support the conclusion that mab-21 acts as part of a mechanism required for correct cell fate choice, possibly involving the function of HOM-C/Hox genes in several body regions.
基因mab-21编码一种由386个氨基酸组成的新型蛋白质,秀丽隐杆线虫雄性尾部的几个细胞选择交替细胞命运需要该基因。从第6条射线前体细胞衍生而来的三个细胞采用前同源细胞的命运,而第四个与谱系无关的皮下细胞则转化为神经母细胞。受影响的细胞共同位于尾部外侧表皮,这表明mab-21作为短程模式形成机制的一部分发挥作用。mab-21突变体引起的细胞命运的每一种变化都可以解释为从后到前的同源异型转化。mab-21突变体雄性和雌雄同体有影响运动、体型和繁殖力的额外多效性表型,这表明mab-21在雄性尾部区域之外具有功能。我们表明,mab-21的三个已知等位基因是一个新基因的亚效等位基因。镶嵌分析表明,mab-21在细胞自主作用下确定感觉射线的特性,但在皮下细胞与神经母细胞命运选择中是非自主作用。细胞消融实验证实了细胞信号传导在神经母细胞命运选择中的存在。先前已表明,mab-21中的突变是HOM-C/Hox基因突变对射线身份指定影响的遗传修饰因子。此处给出的结果支持以下结论:mab-21作为正确细胞命运选择所需机制的一部分发挥作用,可能涉及HOM-C/Hox基因在几个身体区域的功能。