Haas S, Gordon J, Khalili K
Department of Biochemistry and Molecular Biology, Jefferson Institute of Molecular Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania 19107.
Mol Cell Biol. 1993 May;13(5):3103-12. doi: 10.1128/mcb.13.5.3103-3112.1993.
Transcription of the myelin basic protein (MBP) gene is regulated in a cell-type-specific and developmental stage-specific manner during myelin formation in the murine central nervous system. The 5'-flanking region of the MBP gene contains several regulatory elements that differentially contribute to the cell-type-specific transcription of MBP in cells derived from the central nervous system. The proximal element, termed MB1, which is located between nucleotides -14 and -50 with respect to the RNA start site, has previously been shown to have characteristics of a cell-type-specific enhancer element. In this study, we used band shift and UV cross-linking assays to identify DNA-binding proteins in mouse brain nuclear extract which interact with the MB1 element. Fractionation of these extracts has allowed the identification of a 38- to 41-kDa nuclear protein, derived from mouse brain tissue at the peak of myelination, which specifically binds the MB1 DNA sequence. Fractions enriched in the MB1-binding protein have been shown to stimulate transcription of the MBP promoter in extract derived from HeLa cells. MB1 binding protein activity is expressed in a tissue-specific and development stage-specific pattern which coincides with the pattern of MBP transcription, suggesting that this protein may be a biologically relevant transcription factor for the MBP gene in vivo.
在小鼠中枢神经系统髓鞘形成过程中,髓鞘碱性蛋白(MBP)基因的转录以细胞类型特异性和发育阶段特异性的方式受到调控。MBP基因的5'侧翼区域包含几个调控元件,它们对中枢神经系统来源细胞中MBP的细胞类型特异性转录有不同的贡献。近端元件,称为MB1,相对于RNA起始位点位于核苷酸-14至-50之间,先前已显示具有细胞类型特异性增强子元件的特征。在本研究中,我们使用凝胶迁移和紫外线交联试验来鉴定小鼠脑海核提取物中与MB1元件相互作用的DNA结合蛋白。对这些提取物进行分级分离,已鉴定出一种38至41 kDa的核蛋白,它来源于髓鞘形成高峰期的小鼠脑组织,能特异性结合MB1 DNA序列。富含MB1结合蛋白的级分已显示能刺激HeLa细胞提取物中MBP启动子的转录。MB1结合蛋白活性以组织特异性和发育阶段特异性的模式表达,这与MBP转录模式一致,表明该蛋白可能是体内MBP基因生物学上相关的转录因子。