Locke J, Tartof K D
Department of Genetics, University of Alberta, Edmonton, Canada.
Mol Gen Genet. 1994 Apr;243(2):234-43. doi: 10.1007/BF00280321.
The cubitus interruptus (ci) locus of Drosophila melanogaster is located proximally on chromosome 4. In ci mutants cubital wing veins are interrupted or absent. We have cloned this locus using a gypsy element associated with the ci1 mutation. Analysis of all extant ci mutations reveals that they contain conspicuous molecular alterations within a 13.7 kb region. Of the four homozygous viable mutations, three (ci1, ci361, ciw) have single insertions, while one (ci57g) has a small deletion, all located within a more restricted 1 kb region. The dominant mutations, ciD and Ce2 each contain two insertions within the 13.7 kb region. All these molecular alterations are located upstream of a transcript previously associated with the ciD mutation and thought to derive from a segment polarity gene. We induced revertants of the dominant ci phenotype (wing vein interruption) in ciD and found molecular alterations in this transcript (the ci+ transcript) in two revertant alleles, thereby demonstrating this transcript's involvement in the ci phenotype. The locations of the molecular alterations, together with the results of the ciD reversion experiment, provide a connection between the dominant and recessive ci mutations and argue that all are likely to be alleles of the same complex locus, ci, not two separate loci as previously proposed. The ci phenotype of dominant and recessive mutations can be explained by inappropriate expression of the ci+ transcript in the posterior wing compartment where the cubital vein is affected, while loss of ci+ function generates recessive lethality. Lack of repression of ci+ transcription, through a pairing-dependent, trans-acting silencer element, can explain the unusual position effects associated with ci (the Dubinin effect).
黑腹果蝇的肘脉中断(ci)基因座位于4号染色体近端。在ci突变体中,肘脉翅脉会中断或缺失。我们利用与ci1突变相关的gypsy元件克隆了这个基因座。对所有现存的ci突变进行分析发现,它们在一个13.7 kb的区域内存在明显的分子改变。在四个纯合存活突变中,三个(ci1、ci361、ciw)有单个插入,而一个(ci57g)有一个小缺失,所有这些都位于一个更受限的1 kb区域内。显性突变ciD和Ce2在13.7 kb区域内各有两个插入。所有这些分子改变都位于一个先前与ciD突变相关且被认为源自一个体节极性基因的转录本的上游。我们在ciD中诱导出显性ci表型(翅脉中断)的回复体,并在两个回复体等位基因中发现了该转录本(ci+转录本)的分子改变,从而证明了该转录本与ci表型有关。分子改变的位置,连同ciD回复实验的结果,建立了显性和隐性ci突变之间的联系,并表明所有这些可能都是同一个复合基因座ci的等位基因,而不是如先前所提出的两个独立基因座。显性和隐性突变的ci表型可以通过ci+转录本在肘脉受影响的后翅区室中不适当的表达来解释,而ci+功能的丧失会导致隐性致死。通过一个配对依赖的反式作用沉默元件对ci+转录的抑制缺失,可以解释与ci相关的不寻常位置效应(杜比宁效应)。