Bel S, Coré N, Djabali M, Kieboom K, Van der Lugt N, Alkema M J, Van Lohuizen M
Centre d'immunologie INSERM-CNRS de Marseille Luminy, Case 906, France.
Development. 1998 Sep;125(18):3543-51. doi: 10.1242/dev.125.18.3543.
In Drosophila and mouse, Polycomb group genes are involved in the maintenance of homeotic gene expression patterns throughout development. Here we report the skeletal phenotypes of compound mutants for two Polycomb group genes bmi1 and M33. We show that mice deficient for both bmi1 and M33 present stronger homeotic transformations of the axial skeleton as compared to each single Polycomb group mutant, indicating strong dosage interactions between those two genes. These skeletal transformations are accompanied with an enhanced shift of the anterior limit of expression of several Hox genes in the somitic mesoderm. Our results demonstrate that in mice the Polycomb group genes act in synergy to control the nested expression pattern of some Hox genes in somitic mesodermal tissues during development.
在果蝇和小鼠中,多梳蛋白家族基因参与了整个发育过程中同源异型基因表达模式的维持。在此,我们报告了两个多梳蛋白家族基因bmi1和M33的复合突变体的骨骼表型。我们发现,与每个单一的多梳蛋白家族突变体相比,同时缺乏bmi1和M33的小鼠轴向骨骼出现了更强的同源异型转化,这表明这两个基因之间存在强烈的剂量相互作用。这些骨骼转化伴随着体节中胚层中几个Hox基因表达前界的增强移位。我们的结果表明,在小鼠中,多梳蛋白家族基因协同作用,在发育过程中控制体节中胚层组织中一些Hox基因的嵌套表达模式。