Tretiakova A, Gallia G L, Shcherbik N, Jameson B, Johnson E M, Amini S, Khalili K
Center for NeuroVirology and NeuroOncology, Allegheny University of the Health Sciences, Philadelphia, Pennsylvania 19102, USA.
J Biol Chem. 1998 Aug 28;273(35):22241-7. doi: 10.1074/jbc.273.35.22241.
Cell type and developmental stage expression of the myelin basic protein (MBP) gene in mouse brain is regulated at the transcriptional level. Earlier studies from our laboratory have led to the identification of a DNA binding protein from mouse brain, named Puralpha, which interacts with the MB1 regulatory motif of the MBP and stimulates its transcription in glial cells. In this report, we demonstrate that a cellular RNA, with significant homology to 7 SL RNA is associated with Puralpha. Results from band shift competition studies indicate that Puralpha-associated RNA (PU-RNA), inhibits the interaction of immunopurified Puralpha with the MB1 DNA sequence. Results from Northern blot studies indicated that PU-RNA is expressed during various stages of brain development. Of interest, this RNA was found in association with Puralpha that was produced in the mouse brain at the early stage of brain development. Results from Northwestern analysis using a PU-RNA probe identified the regions within Puralpha that are important for Puralpha/PU-RNA association. Production of Puralpha at the early stage of brain development and its association with PU-RNA at this stage, when Puralpha exhibits poor binding ability to the MB1 DNA sequence, suggests that PU-RNA may function as a co-factor that negatively regulates Puralpha interaction with the MBP promoter sequence.
小鼠脑中髓鞘碱性蛋白(MBP)基因的细胞类型和发育阶段表达在转录水平受到调控。我们实验室早期的研究已鉴定出一种来自小鼠脑的DNA结合蛋白,名为Puralpha,它与MBP的MB1调控基序相互作用,并刺激其在神经胶质细胞中的转录。在本报告中,我们证明了一种与7 SL RNA具有显著同源性的细胞RNA与Puralpha相关联。凝胶迁移竞争研究结果表明,与Puralpha相关的RNA(PU-RNA)抑制免疫纯化的Puralpha与MB1 DNA序列的相互作用。Northern印迹研究结果表明,PU-RNA在脑发育的各个阶段均有表达。有趣的是,这种RNA与在脑发育早期小鼠脑中产生的Puralpha相关联。使用PU-RNA探针进行的蛋白质印迹分析结果确定了Puralpha中对Puralpha/PU-RNA关联重要的区域。在脑发育早期产生Puralpha并在此阶段使其与PU-RNA相关联,而此时Puralpha对MB1 DNA序列的结合能力较差,这表明PU-RNA可能作为一种辅助因子负向调节Puralpha与MBP启动子序列的相互作用。