Campagnoni A T
Mental Retardation Research Center, UCLA School of Medicine 90024.
J Neurochem. 1988 Jul;51(1):1-14. doi: 10.1111/j.1471-4159.1988.tb04827.x.
Within the past several years, several of the genes coding for the major myelin proteins have been isolated, characterized, and mapped to specific chromosomes. In all cases, it has been clearly established that these proteins exist as multiple isoforms, and their structures have been established through an analysis of the cDNA clones encoding them. In each case, the isoforms appear to arise through the translation of individual mRNAs produced by alternative splicing of the primary transcript of a single gene. In several cases, the expression of the individual isoforms appears to be developmentally and/or regionally regulated, probably at the level of the splicing of the primary transcript. In the case of the dysmyelinating mutants shiverer and jimpy, the molecular defects involve the MBP gene and PLP gene, respectively; most of the dysmyelinating mutants, including those in which the genetic defect is established, appear to exhibit pleiotropy with respect to the expression of other myelin protein genes.
在过去几年中,编码主要髓磷脂蛋白的几个基因已被分离、鉴定并定位到特定染色体上。在所有情况下,都已明确这些蛋白质以多种异构体形式存在,并且它们的结构已通过对编码它们的cDNA克隆进行分析得以确定。在每种情况下,异构体似乎是由单个基因初级转录本的可变剪接产生的单个mRNA翻译而来。在几种情况下,各个异构体的表达似乎受到发育和/或区域调控,可能在初级转录本剪接水平上。就脱髓鞘突变体颤抖者和跳跃者而言,分子缺陷分别涉及髓磷脂碱性蛋白(MBP)基因和蛋白脂蛋白(PLP)基因;大多数脱髓鞘突变体,包括那些已确定遗传缺陷的突变体,在其他髓磷脂蛋白基因的表达方面似乎表现出多效性。