Kunimoto M
Environmental Health Sciences Division, National Institute for Environmental Studies, Ibaraki, Japan.
J Cell Biol. 1995 Dec;131(6 Pt 2):1821-9. doi: 10.1083/jcb.131.6.1821.
Two isoforms of brain ankyrin, 440- and 220- kD ankyrinB, are generated from the same gene by alternative splicing of pre-mRNA. The larger isoform shares the same NH2-terminal and COOH-terminal domains to the smaller isoform and contains, in addition, a unique inserted domain of about 220-kD in size (Kunimoto, M., E. Otto, and V. Bennett. 1991. J. Cell Biol. 115:1319-1331). Both Isoforms were expressed in primary cerebellar cells in a manner similar to that in vivo; the larger isoform appeared first when axogenesis is actively conducted and the smaller isoform came up later. 440-kD ankyrinB was localized in the axons of cerebellar neurons both in vivo and in vitro using an antibody raised against the insert region, while 220-kD isoform was rather localized in the cell bodies and dendrites of neurons by a specific antibody prepared using a synthetic peptide corresponding to the splice site as antigen. Astroglia cells also expressed 220-kD ankyrinB but not the 440-kD isoform. These results indicate that 440-kD ankyrinB is a neuron-specific isoform targeted to the axons and its unique inserted domain is essential for the targeting.
脑锚蛋白的两种同工型,即440kD和220kD的锚蛋白B,是由同一基因通过前体mRNA的可变剪接产生的。较大的同工型与较小的同工型具有相同的氨基末端和羧基末端结构域,此外还包含一个大小约为220kD的独特插入结构域(Kunimoto, M., E. Otto, and V. Bennett. 1991. J. Cell Biol. 115:1319 - 1331)。两种同工型在原代小脑细胞中的表达方式与体内相似;较大的同工型在轴突发生活跃时首先出现,较小的同工型随后出现。使用针对插入区域产生的抗体,440kD的锚蛋白B在体内和体外均定位于小脑神经元的轴突中,而220kD的同工型则通过使用对应于剪接位点的合成肽作为抗原制备的特异性抗体定位于神经元的细胞体和树突中。星形胶质细胞也表达220kD的锚蛋白B,但不表达440kD的同工型。这些结果表明,440kD的锚蛋白B是一种靶向轴突的神经元特异性同工型,其独特的插入结构域对于靶向作用至关重要。