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三个相邻基因与泛素连接酶复合体及刚毛-类刚毛位点相互作用,以影响果蝇成虫盘的形态发生。

Three neighboring genes interact with the Broad-Complex and the Stubble-stubbloid locus to affect imaginal disc morphogenesis in Drosophila.

作者信息

Gotwals P J, Fristrom J W

机构信息

Department of Molecular and Cellular Biology, University of California, Berkeley 94720.

出版信息

Genetics. 1991 Apr;127(4):747-59. doi: 10.1093/genetics/127.4.747.

Abstract

The Broad-Complex (BR-C) is a complex regulatory locus at 2B-5 on the X chromosome of Drosophila melanogaster. The wild-type BR-C products are apparent transcription factors necessary for imaginal disc morphogenesis. Alleles of the Stubble-stubbloid (Sb-sbd) locus at 89B9-10 act as dominant enhancers of broad alleles of the BR-C. Sb-sbd wild-type products are necessary for appendage elongation. We report, here, on three new loci implicated in imaginal disc morphogenesis based on their genetic interactions with both BR-C and/or Sb-sbd mutants. Enhancer of broad (E(br)) was identified as a dominant enhancer of the br1 allele of the BR-C and is a recessive lethal. Mapping of E(br) has led to the identification of two loci, blistered and l(2)B485, mutants of which interact with E(br) and the Sb-sbd locus. Blistered, but not l(2)B485, interacts strongly with the BR-C. Alleles of the blistered locus are viable and disrupt proper wing disc morphogenesis independent of genetic interactions. All three loci map within the 0.6-map unit interval between the genetic markers speck and Irregular facets and to the cytological region 60C5-6; 60E9-10 at the tip of chromosome 2R. Genetic evidence is consistent with the view that the BR-C regulates blistered.

摘要

泛复合体(BR-C)是黑腹果蝇X染色体上2B-5处的一个复杂调控位点。野生型BR-C产物是成虫盘形态发生所必需的明显转录因子。位于89B9-10的刚毛-类刚毛(Sb-sbd)位点的等位基因作为BR-C广泛等位基因的显性增强子。Sb-sbd野生型产物是附肢伸长所必需的。我们在此报告基于它们与BR-C和/或Sb-sbd突变体的遗传相互作用而涉及成虫盘形态发生的三个新位点。泛增强子(E(br))被鉴定为BR-C的br1等位基因的显性增强子,并且是隐性致死的。E(br)的定位导致鉴定出两个位点,即起泡和l(2)B485,它们的突变体与E(br)和Sb-sbd位点相互作用。起泡而非l(2)B485与BR-C强烈相互作用。起泡位点的等位基因是有活力的,并且独立于遗传相互作用破坏适当的翅盘形态发生。所有这三个位点都定位在遗传标记斑点和不规则小眼之间0.6个图距单位的区间内,位于2R染色体末端的细胞学区域60C5-6;60E9-10。遗传证据与BR-C调节起泡的观点一致。

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