Klämbt C, Knust E, Tietze K, Campos-Ortega J A
Institut für Entwicklungsphysiologie, Universität zu Köln, FRG.
EMBO J. 1989 Jan;8(1):203-10. doi: 10.1002/j.1460-2075.1989.tb03365.x.
Genetic evidence suggests that E(spl), one of the neurogenic loci of Drosophila, is a gene complex comprising an as yet incompletely established number of transcription units. In order to correlate the various transcription units with E(spl) functions, wild-type flies were transformed with genomic DNA encoding the transcription unit m8 from the mutant E(spl)D, which was known to be altered in embryos carrying this mutant allele. Transformants show the same dominant enhancement of the spl phenotype as E(spl)D itself. Since m8 has a virtually identical pattern of expression as m4, m5 and m7, we have determined the sequence of these four transcripts. The deduced protein products of m5, m7 and m8 exhibit extensive sequence homology with each other. All three encode a sequence similar to one of the conserved domains of representatives of the vertebrate myc gene family which is also present in the deduced protein sequences of the Drosophila achaete-scute gene complex. Sequence analysis of the m8 transcription unit in the E(spl)D mutation revealed several DNA lesions. One of the lesions is a deletion in the region upstream of the transcription start site. Another lesion is a deletion in the coding region that leads to a shorter protein which, in addition, differs in its carboxy-terminal end from the wild-type protein by the presence of nine amino acids.
遗传学证据表明,果蝇的神经发生位点之一E(spl)是一个基因复合体,其转录单元的数量尚未完全确定。为了将各种转录单元与E(spl)的功能联系起来,用编码来自突变体E(spl)D的转录单元m8的基因组DNA转化野生型果蝇,已知在携带该突变等位基因的胚胎中m8发生了改变。转化体表现出与E(spl)D本身相同的对spl表型的显性增强作用。由于m8与m4、m5和m7具有几乎相同的表达模式,我们测定了这四个转录本的序列。m5、m7和m8推导的蛋白质产物彼此表现出广泛的序列同源性。这三个都编码一个与脊椎动物myc基因家族代表的一个保守结构域相似的序列,该结构域也存在于果蝇achaete-scute基因复合体的推导蛋白质序列中。对E(spl)D突变中m8转录单元的序列分析揭示了几个DNA损伤。其中一个损伤是转录起始位点上游区域的缺失。另一个损伤是编码区的缺失,导致产生一种较短的蛋白质,此外,其羧基末端与野生型蛋白质不同,多了九个氨基酸。