Wulf P, Bernhardt R R, Suter U
Institute of Cell Biology, Department of Biology, Swiss Federal Institute of Technology, Zurich, Switzerland.
J Neurosci Res. 1999 Aug 15;57(4):467-78.
Peripheral myelin protein 22 (PMP22) is a component of compact myelin of the peripheral nervous system (PNS). Mutations affecting PMP22 are associated with hereditary neuropathies in humans and rodents. Although mammalian PMP22 is expressed in several tissues, the disease pathology is restricted to the PNS. We describe the characterization of a PMP22-related cDNA from zebrafish and the distribution of its cognate mRNA. Phylogenetic considerations and mRNA expression in cranial nerves are consistent with the interpretation that the encoded protein is the orthologue of mammalian PMP22. In situ hybridization analysis during development showed zebrafish PMP22 expression in embryonic sclerotome cells, in neural crest cells, and in migratory derivatives of both populations. Based on this specific expression pattern prior to the onset of myelination, we hypothesize that zebrafish PMP22 may play a role in early PNS development and that disturbance of such functions may contribute to the PNS-restricted defects caused by mutations in the mammalian PMP22 gene.
外周髓鞘蛋白22(PMP22)是外周神经系统(PNS)致密髓鞘的一个组成部分。影响PMP22的突变与人类和啮齿动物的遗传性神经病变有关。尽管哺乳动物的PMP22在多个组织中表达,但疾病病理仅限于PNS。我们描述了来自斑马鱼的PMP22相关cDNA的特征及其同源mRNA的分布。系统发育分析和在颅神经中的mRNA表达与所编码的蛋白质是哺乳动物PMP22的直系同源物这一解释一致。发育过程中的原位杂交分析表明,斑马鱼PMP22在胚胎期的体节细胞、神经嵴细胞以及这两个群体的迁移衍生物中表达。基于髓鞘形成开始之前的这种特定表达模式,我们推测斑马鱼PMP22可能在PNS早期发育中发挥作用,并且这种功能的紊乱可能导致哺乳动物PMP22基因突变引起的PNS局限性缺陷。