Cheng N N, Sinclair D A, Campbell R B, Brock H W
Department of Zoology, University of British Columbia, Vancouver, Canada.
Genetics. 1994 Dec;138(4):1151-62. doi: 10.1093/genetics/138.4.1151.
The Polycomb (Pc) group genes of Drosophila are negative regulators of homeotic genes, but individual loci have pleiotropic phenotypes. It has been suggested that Pc group genes might form a regulatory hierarchy, or might be members of a multimeric complex that obeys the law of mass action. Recently, it was shown that polyhomeotic (ph) immunoprecipitates in a multimeric complex that includes Pc. Here, we show that duplications of ph suppress homeotic transformations of Pc and Pcl, supporting a mass-action model for Pc group function. We crossed ph alleles to all members of the Polycomb group, and to E(Pc) and Su(z)2 to look for synergistic effects. We observed extragenic noncomplementation between ph503 and Pc, Psc1 and Su(z)2(1) in females, and between ph409 and Sce1, ScmD1 and E(z)1 mutations in males, suggesting that these gene products might interact directly with ph. Males hemizygous for a temperature-sensitive allele, ph2, are lethal when heterozygous with mutants in Asx, Pc, Pcl, Psc, Sce and Scm, and with E(Pc) and Su(z)2. Mutations in trithorax group genes were not able to suppress the lethality of ph2/Y; Psc1/+ males. ph2 was not lethal with extra sex combs, E(z), super sex combs (sxc) or l(4)102EFc heterozygotes, but did cause earlier lethality in embryos homozygous for E(z), sxc and l(4)102EFc. However, ph503 did not enhance homeotic phenotypes of esc heterozygotes derived from homozygous esc- mothers. We examined the embryonic phenotypes of ph2 embryos that were lethal when heterozygous or homozygous for other mutations. Based on this phenotypic analysis, we suggest that ph may perform different functions in conjunction with differing subsets of Pc group genes.
果蝇的多梳(Pc)组基因是同源异型基因的负调控因子,但单个基因座具有多效性表型。有人提出,Pc组基因可能形成一个调控层次结构,或者可能是一个遵循质量作用定律的多聚体复合物的成员。最近,研究表明多同源异型(ph)在一个包含Pc的多聚体复合物中进行免疫沉淀。在这里,我们表明ph的重复抑制了Pc和Pcl的同源异型转化,支持了Pc组功能的质量作用模型。我们将ph等位基因与多梳组的所有成员以及E(Pc)和Su(z)2杂交,以寻找协同效应。我们在雌性中观察到ph503与Pc、Psc1与Su(z)2(1)之间的基因外互补缺失,在雄性中观察到ph409与Sce1、ScmD1与E(z)1突变之间的基因外互补缺失,这表明这些基因产物可能直接与ph相互作用。对于温度敏感等位基因ph2半合子的雄性,当与Asx、Pc、Pcl、Psc、Sce和Scm的突变体以及E(Pc)和Su(z)2杂合时是致死的。三体胸组基因的突变不能抑制ph2/Y;Psc1/+雄性的致死性。ph2与额外性梳、E(z)、超级性梳(sxc)或l(4)102EFc杂合子不致死,但确实会导致E(z)、sxc和l(4)102EFc纯合胚胎更早死亡。然而,ph503并没有增强来自纯合esc-母亲的esc杂合子的同源异型表型。我们检查了ph2胚胎的胚胎表型,当这些胚胎与其他突变杂合或纯合时是致死的。基于这种表型分析,我们认为ph可能与Pc组基因的不同子集结合执行不同的功能。