Snipes G J, Suter U, Welcher A A, Shooter E M
Department of Neurobiology, Stanford University School of Medicine, CA 94305.
J Cell Biol. 1992 Apr;117(1):225-38. doi: 10.1083/jcb.117.1.225.
We have recently described a novel cDNA, SR13 (Welcher, A. A., U. Suter, M. De Leon, G. J. Snipes, and E. M. Shooter. 1991. Proc. Natl. Acad. Sci. USA. 88:7195-7199), that is repressed after sciatic nerve crush injury and shows homology to both the growth arrest-specific mRNA, gas3 (Manfioletti, G., M. E. Ruaro, G. Del Sal, L. Philipson, and C. Schneider, 1990. Mol. Cell Biol. 10:2924-2930), and to the myelin protein, PASII (Kitamura, K., M. Suzuki, and K. Uyemura. 1976. Biochim. Biophys. Acta. 455:806-816). In this report, we show that the 22-kD SR13 protein is expressed in the compact portion of essentially all myelinated fibers in the peripheral nervous system. Although SR13 mRNA was found in the central nervous system, no corresponding SR13 protein could be detected by either immunoblot analysis or by immunohistochemistry. Northern and immunoblot analysis of SR13 mRNA and protein expression during development of the peripheral nervous system reveal a pattern similar to other myelin proteins. Furthermore, we demonstrate by in situ mRNA hybridization on tissue sections and on individual nerve fibers that SR13 mRNA is produced predominantly by Schwann cells. We conclude that the SR13 protein is apparently exclusively expressed in the peripheral nervous system where it is a major component of myelin. Thus, we propose the name Peripheral Myelin Protein-22 (PMP-22) for the proteins and cDNA previously designated PASII, SR13, and gas3.
我们最近描述了一种新的cDNA,即SR13(韦尔彻,A.A.,U.苏特,M.德莱昂,G.J.斯奈普斯,以及E.M.舒特。1991年。美国国家科学院院刊。88:7195 - 7199),它在坐骨神经挤压损伤后受到抑制,并且与生长停滞特异性mRNA即gas3(曼菲奥莱蒂,G.,M.E.鲁阿罗,G.德尔萨尔,L.菲利普森,以及C.施奈德,1990年。分子细胞生物学。10:2924 - 2930)以及髓磷脂蛋白PASII(北村,K.,M.铃木,以及K.上村。1976年。生物化学与生物物理学报。455:806 - 816)均具有同源性。在本报告中,我们表明22-kD的SR13蛋白表达于外周神经系统中基本上所有有髓纤维的致密部分。尽管在中枢神经系统中发现了SR13 mRNA,但通过免疫印迹分析或免疫组织化学均未检测到相应的SR13蛋白。对外周神经系统发育过程中SR13 mRNA和蛋白表达的Northern印迹和免疫印迹分析揭示了一种与其他髓磷脂蛋白相似的模式。此外,我们通过对组织切片和单个神经纤维进行原位mRNA杂交证明,SR13 mRNA主要由施万细胞产生。我们得出结论,SR13蛋白显然仅在外周神经系统中表达,在那里它是髓磷脂的主要成分。因此,我们为先前命名为PASII、SR13和gas3的蛋白质及cDNA提议命名为外周髓磷脂蛋白-22(PMP-22)。