Leviten M W, Posakony J W
Department of Biology, University of California San Diego, La Jolla, 92093-0366, USA.
Dev Biol. 1996 Jun 15;176(2):264-83. doi: 10.1006/dbio.1996.0133.
We have isolated a novel class of gain-of-function mutations at the Bearded (Brd) locus which specifically affect the development of adult sensory organs in Drosophila. These Brd alleles cause bristle multiplication and bristle loss phenotypes resembling those described for the neurogenic genes Notch (N) and Delta (Dl). We have found that supernumerary sensory organ precursor (SOP) cells develop in the proneural clusters of Brd mutant imaginal discs; like normal SOPs, these are dependent on the function of the proneural genes achaete and scute, and express elevated levels of ac protein. At cuticular positions exhibiting the Brd bristle loss phenotype, we have found that the progeny of the multiplied SOPs develop aberrantly, in that neurons and thecogen (sheath) cells appear but not trichogen (shaft) and tormogen (socket) cells. This appears to represent a transformation of the pIIa secondary precursor cell within the SOP lineage to a pIIb secondary precursor cell fate. These results suggest that Brd gain-of-function alleles interfere with Notch pathway-dependent cell-cell interactions at two distinct stages of adult sensory organ development. We have also identified enhancers and suppressors of the Brd dominant phenotypes; these include both previously characterized mutations and alleles of apparently novel loci. Finally, we have found that Brd null mutants are viable and exhibit no mutant phenotypes, suggesting that Brd may be a component of an overlapping function.
我们在“大胡子”(Brd)基因座分离出了一类新的功能获得性突变,这类突变特异性地影响果蝇成虫感觉器官的发育。这些Brd等位基因导致刚毛增殖和刚毛缺失表型,类似于神经源性基因Notch(N)和Delta(Dl)所描述的表型。我们发现,在Brd突变体成虫盘的原神经簇中会发育出多余的感觉器官前体细胞(SOP);与正常SOP一样,这些细胞依赖于原神经基因achaete和scute的功能,并表达高水平的ac蛋白。在表现出Brd刚毛缺失表型的表皮位置,我们发现增殖的SOP的后代发育异常,即出现了神经元和鞘细胞,但没有毛原细胞(轴)和膜原细胞(窝)。这似乎代表了SOP谱系中的pIIa二级前体细胞向pIIb二级前体细胞命运的转变。这些结果表明,Brd功能获得性等位基因在成虫感觉器官发育的两个不同阶段干扰了Notch信号通路依赖的细胞间相互作用。我们还鉴定出了Brd显性表型的增强子和抑制子;其中包括先前已鉴定的突变以及明显新基因座的等位基因。最后,我们发现Brd基因敲除突变体是可行的,且没有表现出突变表型,这表明Brd可能是一个具有重叠功能的组分。