Kimura M, Inoko H, Katsuki M, Ando A, Sato T, Hirose T, Takashima H, Inayama S, Okano H, Takamatsu K
J Neurochem. 1985 Mar;44(3):692-6. doi: 10.1111/j.1471-4159.1985.tb12870.x.
The gene expression of myelin basic proteins (MBPs) in shiverer mutant mice was investigated by the Northern and Southern hybridization techniques. In the control mice RNA molecules from the brains which were about 2,300 nucleotides in length were hybridized to cDNA of 1.8 kb encoding for a mouse MBP, but RNA from the brains of 3-week-old shiverer mutant mice contained no detectable amount of MBP transcripts hybridizing to this probe. Moreover the shiverer mutant mice lost several restriction fragments that hybridized to the same probe in the control mice when each of the five restriction enzymes, i.e., HindIII, PstI, PvuII, AccI, and StuI, was used. These data suggest that the shiverer mutation may correspond to the deletion of a large portion of MBP exon(s) in the gene, and this deletion causes inefficient transcription leading to the depletion of MBPs in the myelin and the dysmyelination observed in these mice.
通过Northern和Southern杂交技术研究了颤抖突变小鼠中髓鞘碱性蛋白(MBP)的基因表达。在对照小鼠中,来自大脑的约2300个核苷酸长度的RNA分子与编码小鼠MBP的1.8 kb cDNA杂交,但3周龄颤抖突变小鼠大脑中的RNA未检测到与该探针杂交的MBP转录本。此外,当使用五种限制性内切酶(即HindIII、PstI、PvuII、AccI和StuI)中的每一种时,颤抖突变小鼠丢失了几个在对照小鼠中与同一探针杂交的限制性片段。这些数据表明,颤抖突变可能对应于该基因中大部分MBP外显子的缺失,这种缺失导致转录效率低下,从而导致这些小鼠髓鞘中MBP的耗尽和脱髓鞘。