ten Berge D, Brouwer A, Korving J, Martin J F, Meijlink F
Hubrecht Laboratory, Netherlands Institute for Developmental Biology, Uppsalalaan 8, The Netherlands.
Development. 1998 Oct;125(19):3831-42. doi: 10.1242/dev.125.19.3831.
Prx1 and Prx2 are closely related paired-class homeobox genes that are expressed in very similar patterns predominantly in mesenchyme. Prx1 loss-of-function mutants show skeletal defects in skull, limbs and vertebral column (Martin, J. F., Bradley, A. and Olson, E. N. (1995) Genes Dev. 9, 1237-1249). We report here that mice in which Prx2 is inactivated by a lacZ insertion had no skeletal defects, whereas Prx1/Prx2 double mutants showed many novel abnormalities in addition to an aggravation of the Prx1 single mutant phenotype. We found defects in external, middle and inner ear, reduction or loss of skull bones, a reduced and sometimes cleft mandible, and limb abnormalities including postaxial polydactyly and bent zeugopods. A single, or no incisor was present in the lower jaw, and ectopic expression of Fgf8 and Pax9 was found medially in the mandibular arch. A novel method to detect &bgr ;-galactosidase activity in hydroxyethylmethacrylate sections allowed detailed analysis of Prx2 expression in affected structures. Our results suggest a role for Prx genes in mediating epitheliomesenchymal interactions in inner ear and lower jaw. In addition, Prx1 and Prx2 are involved in interactions between perichondrium and chondrocytes that regulate their proliferation or differentiation in the bones of the zeugopods.
Prx1和Prx2是密切相关的配对类同源框基因,主要在间充质中以非常相似的模式表达。Prx1功能丧失突变体在颅骨、四肢和脊柱中表现出骨骼缺陷(Martin, J. F., Bradley, A.和Olson, E. N. (1995) Genes Dev. 9, 1237 - 1249)。我们在此报告,通过lacZ插入使Prx2失活的小鼠没有骨骼缺陷,而Prx1/Prx2双突变体除了Prx1单突变体表型加重外,还表现出许多新的异常。我们发现外耳、中耳和内耳存在缺陷,颅骨减少或缺失,下颌骨减少且有时出现腭裂,以及四肢异常,包括轴后多指和挠骨与胫骨弯曲。下颌骨中存在一颗或没有门牙,并且在下颌弓内侧发现了Fgf8和Pax9的异位表达。一种在甲基丙烯酸羟乙酯切片中检测β - 半乳糖苷酶活性的新方法允许对受影响结构中Prx2的表达进行详细分析。我们的结果表明Prx基因在介导内耳和下颌骨的上皮 - 间充质相互作用中发挥作用。此外,Prx1和Prx2参与了骨膜与软骨细胞之间的相互作用,这些相互作用调节了挠骨与胫骨骨骼中软骨细胞的增殖或分化。