Weigel Detlef, Bellen Hugo J, Jürgens Gerd, Jäckle Herbert
Institut für Genetik und Mikrobiologie, Universität München, Maria-Ward-Straß e la, D-8000, München 19, Germany.
Biozentrum der Universität, Klingelbergstraße 70, CH-4056, Basel, Switzerland.
Rouxs Arch Dev Biol. 1989 Nov;198(4):201-210. doi: 10.1007/BF00375906.
The homeotic gene fork head (fkh) of Drosophila melanogaster promotes terminal as opposed to segmental development in the ectodermal parts of the gut. Molecular analysis revealed that fkh expression is not restricted to the ectodermal parts of the gut, but is detectable in a variety of other tissues. Therefore, the phenotype of fkh mutant embryos was re-examined using molecular probes as tissue specific markers. With the exception of the nervous system, which was not studied, phenotypic effects were found in all tissues expressing fkh protein in the wild-type. Particularly, these tissues include all components of the gut in the Drosophila embryo: the foregut and hindgut, the midgut and the yolk nuclei. The defects observed in the gut of fkh mutant embryos are primordium specific.
果蝇的同源异型基因叉头(fkh)促进肠道外胚层部分的末端发育,而非节段发育。分子分析表明,fkh的表达并不局限于肠道的外胚层部分,在多种其他组织中也可检测到。因此,使用分子探针作为组织特异性标记,对fkh突变胚胎的表型进行了重新检查。除未研究的神经系统外,在野生型中表达fkh蛋白的所有组织中均发现了表型效应。特别地,这些组织包括果蝇胚胎肠道的所有组成部分:前肠和后肠、中肠和卵黄核。在fkh突变胚胎肠道中观察到的缺陷是原基特异性的。