髓鞘碱性蛋白的分子生物学:髓鞘缺乏突变体中基因重排和反义RNA的表达。

K Mikoshiba, J Aruga, H Okano
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引用次数: 0

摘要

1. 髓磷脂是中枢神经系统(CNS)和外周神经系统(PNS)中促进沿轴突传导冲动的重要结构。2. 髓鞘碱性蛋白(Myelin basic protein, MBP)是中枢神经系统髓鞘中的一种主要蛋白。3.MBP在神经系统中特异表达。4. MBP基因已被克隆并鉴定。5. 两种突变小鼠,Shiverer (shi)和髓磷脂缺乏(mld)。Shimid),是常染色体隐性突变,表现出严重的症状,如故意震颤。他们被发现有MBP基因突变,导致中枢神经系统髓鞘形成不良。6. 发现MBP基因内的重排导致该基因的低表达。7. 在Shiverer中,MBP基因被部分删除(从外显子3到7),而在mld中,该基因被串联复制,并且大部分复制在完整拷贝的上游反转。8. 在mld中,RNase保护研究中检测到与3-7外显子互补的反义RNA,该反义RNA与倒置片段相对应,被认为是导致MBP表达降低的原因。9. 并对MBP基因重排的机制进行了探讨。10. 本文综述了近年来MBP基因的研究进展,特别是该基因的重排及其在突变小鼠中的表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular biology of myelin basic protein: gene rearrangement and expression of anti-sense RNA in myelin-deficient mutants.

1. Myelin is an important structure for facilitating the conduction of impulses along the axons both in the central nervous system (CNS) and peripheral nervous system (PNS). 2. Myelin basic protein (MBP) is a major protein in CNS myelin. 3. MBP is expressed specifically in the nervous system. 4. The MBP gene has been cloned and characterized. 5. Two mutant mice, Shiverer (shi) and myelin-deficient (mld. shimid), are autosomal recessive mutants that show severe symptoms such as intentional tremor. They have been found to have a mutation in the MBP gene that results in poor myelination in the central nervous system. 6. It was found that rearrangement within the MBP gene results in low expression of the gene. 7. In Shiverer, the MBP gene is partially deleted (from exons 3 to 7), and in mld, the gene is duplicated tandemly and a large portion of the duplication is inverted upstream of the intact copy. 8. In mld, anti-sense RNA complementary to exons 3-7, which correspond to the inverted segment, was detected by RNase protection studies, and presumed to be responsible for the reduced expressions of MBP. 9. The mechanism of gene rearrangement in MBP was also characterized. 10. This article reviews the recent progress in the study of the MBP gene, especially the rearrangement of the gene and its expression in mutant mice.

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