Department of Biology, Program in Genetics, Indiana University, Bloomington, Indiana 47405.
Genetics. 1980 Jun;95(2):383-97. doi: 10.1093/genetics/95.2.383.
The existence of a gene complex in the proximal right arm of chromosome 3 of Drosophila melanogaster involved in the development of the head and thorax was originally suggested by the phenotypes of several dominant homoeotic mutations and their revertants. A screen for mutations utilizing Df(3R) Antp(Ns+R17) (proximally broken in salivary region 84B1,2) yielded, among 102 recovered mutations, 17 localized by deficiency mapping to the putative homoeotic cluster. These fell into four complementation groups, two of which were characterized by homoeotic phenotypes. To explore the limits of the Antennapedia gene complex (ANT-C) more proximally, a second screen has been undertaken utilizing Df(3R)Scr, a deficiency of 84A1-B1,2.-Of 2832 chromosomes screened, 21 bearing alterations localized to polytene interval 84A-84B1,2 have been recovered. Sixteen are recessive lethals, and five showing reduced viability display a visible phenotype in surviving individuals. Complementation and phenotypic analyses revealed four complementation groups proximal to those identified in the previous screen, including two new alleles of the recessive homoeotic mutation, proboscipedia (pb). Ten of the new mutations correspond to complementation groups defined previously in the Df(3R)Antp(Ns+R17) screen four to the EbR11 group, two to the Scr group and four to the Antp group.-On the basis of the phenotypes of the 39 mutations localized to this region, plus their interactions with extant homoeotic mutations, we postulate that there are at least five functional sites comprising the ANT-C. Three have been demonstrated to be homoeotic in nature. The specific homoeotic transformations thus far observed suggest that these loci are critical for normal development of adult labial, maxillary and thoracic structures.
果蝇第 3 号染色体近着丝粒区的一个基因复合体与头部和胸部的发育有关,这一事实最初是由几个显性同异位突变及其回复突变的表型所提示的。利用 Df(3R)Antp(Ns+R17)(在唾液区 84B1,2 处近着丝粒断裂)筛选突变体,在所恢复的 102 个突变体中,有 17 个通过缺失作图定位在假定的同异位簇内。这些突变体分为四个互补群,其中两个群的表型具有同异位特征。为了更靠近触角足基因复合体(ANT-C)的近端进行限制,利用 Df(3R)Scr(84A1-B1,2 的缺失)进行了第二次筛选。在筛选的 2832 条染色体中,有 21 条携带的改变定位于多线染色体间隔 84A-84B1,2,已回收。其中 16 个是隐性致死突变,5 个显示生存个体的存活能力降低的表型。互补和表型分析揭示了与前一次筛选中鉴定的那些基因簇靠近的四个互补群,包括隐性同异位突变 proboscipedia (pb) 的两个新等位基因。新突变中有 10 个对应于以前在 Df(3R)Antp(Ns+R17)筛选中定义的互补群,4 个对应于 EbR11 群,2 个对应于 Scr 群,4 个对应于 Antp 群。基于定位在这个区域的 39 个突变的表型,以及它们与现存的同异位突变的相互作用,我们假设至少有五个功能位点组成了 ANT-C。其中三个已被证明具有同异位性质。迄今为止观察到的特定同异位转换表明,这些基因座对于成年唇瓣、上颌和胸部结构的正常发育是至关重要的。