Sanicola M, Sekelsky J, Elson S, Gelbart W M
Department of Cellular and Developmental Biology, Harvard University, Cambridge, Massachusetts 02138, USA.
Genetics. 1995 Feb;139(2):745-56. doi: 10.1093/genetics/139.2.745.
During development of the Drosophila adult appendage precursors, the larval imaginal disks, the decapentaplegic (dpp) gene is expressed in a stripe just anterior to the anterior/posterior (A/P) compartment boundary. Here, we investigate the genetic controls that lead to production of this stripe. We extend previous observations on leaky engrailed (en) mutations by showing that mutant clones completely lacking both en and invected (inv) activity ectopically express dpp-lacZ reporter genes in the posterior compartment, where dpp activity ordinarily is repressed. Similarly, patched (ptc) is also ectopically expressed in such posterior compartment en-inv- null clones. In contrast, these en-inv- clones exhibit loss of hedgehog (hh) expression. We suggest that the absence of dpp expression in the posterior compartment is due to direct repression by en. Ubiquitious expression of en in imaginal disks, produced by a hs-en construct, eliminates the expression of dpp-lacZ in its normal A/P boundary stripe. We identify three in vitro Engrailed binding sites in one of our dpp-lacZ reporter gene. Mutagenesis of these Engrailed binding sites results in ectopic expression of this reporter gene, but does not alter the normal stripe of expression at the A/P boundary. We propose that the en-hh-ptc regulatory loop that is responsible for segmental expression of wingless in the embryo is reutilized in imaginal disks to create a stripe of dpp expression along the A/P compartment boundary.
在果蝇成虫附肢前体(即幼虫的成虫盘)发育过程中,“十体瘫”(dpp)基因在前后(A/P)间隔边界前方的一条带中表达。在此,我们研究导致这条带产生的遗传控制机制。我们通过研究扩展了之前对渗漏型“成对控制基因”(en)突变的观察,结果表明,完全缺乏en和“镶嵌”(inv)活性的突变克隆在通常抑制dpp活性的后间隔中异位表达dpp - lacZ报告基因。同样,“patched”(ptc)在这种后间隔en - inv - 缺失克隆中也异位表达。相反,这些en - inv - 克隆表现出“刺猬”(hh)表达缺失。我们认为后间隔中dpp表达的缺失是由于en的直接抑制作用。由hs - en构建体产生的en在成虫盘中的普遍表达消除了其在正常A/P边界带中的dpp - lacZ表达。我们在我们的一个dpp - lacZ报告基因中鉴定出三个体外“成对控制基因”结合位点。对这些“成对控制基因”结合位点进行诱变导致该报告基因异位表达,但不会改变A/P边界处的正常表达带。我们提出,负责胚胎中“无翅”基因节段性表达的en - hh - ptc调控环在成虫盘中被重新利用,以在A/P间隔边界处形成一条dpp表达带。