Soto M C, Chou T B, Bender W
Harvard Medical School, Department of Biological Chemistry and Molecular Pharmacology, Boston, Massachusetts 02115, USA.
Genetics. 1995 May;140(1):231-43. doi: 10.1093/genetics/140.1.231.
The genes of the Polycomb group (PcG) repress the genes of the bithorax and Antennapedia complexes, among others. To observe a null phenotype for a PcG gene, one must remove its maternal as well as zygotic contribution to the embryo. Five members of the PcG group are compared here: Enhancer of Polycomb [E(Pc)], Additional sex combs (Asx), Posterior sex combs (Psc), Suppressor of zeste 2 [Su (z) 2] and Polycomblike (Pcl). The yeast recombinase (FLP) system was used to induce mitotic recombination in the maternal germline. Mutant embryos were analyzed by staining with antibodies against six target genes of the PcG. The loss of the maternal component leads to enhanced homeotic phenotypes and to unique patterns of misexpression. E(Pc) and Su(z) 2 mutations had only subtle effects on the target genes, even when the maternal contributions were removed. Asx and Pcl mutants show derepression of the targets only in specific cell types. Psc shows unusual effects on two of the targets, Ultrabithorax and abdominal-A. These results show that the PcG genes do not act only in a common complex or pathway; they must have some independent functions.
多梳蛋白组(PcG)的基因会抑制双胸复合体和触角足复合体等的基因。要观察PcG基因的无效表型,必须去除其对胚胎的母体贡献以及合子贡献。本文比较了PcG组的五个成员:多梳增强子[E(Pc)]、额外性梳(Asx)、后性梳(Psc)、zeste 2抑制因子[Su(z)2]和类多梳蛋白(Pcl)。酵母重组酶(FLP)系统用于在母体生殖系中诱导有丝分裂重组。通过用针对PcG的六个靶基因的抗体进行染色来分析突变胚胎。母体成分的缺失会导致同源异型表型增强以及独特的错误表达模式。即使去除了母体贡献,E(Pc)和Su(z)2突变对靶基因也只有细微影响。Asx和Pcl突变体仅在特定细胞类型中表现出靶基因的去抑制。Psc对两个靶基因,即超双胸和腹部-A,表现出不同寻常的影响。这些结果表明,PcG基因并非仅在一个共同的复合体或途径中起作用;它们必定具有一些独立的功能。