Deans Z, Dawson S J, Buttery L, Polak J M, Wallace D, Latchman D S
Department of Molecular Pathology, University College London Medical School, UK.
J Mol Neurosci. 1995;6(3):159-67. doi: 10.1007/BF02736762.
The POU family transcription factor Oct-2 was originally identified in B lymphocytes but has been shown to be expressed in neuronal cells, although it is absent in most other cell types. Cotransfection of Oct-2 expression vectors into nonneuronal cells with a tyrosine hydroxylase promoter/reporter plasmid suggests that Oct-2 can repress this promoter in this artificial situation. Here we report that reduction of endogenous Oct-2 levels in a neuronal cell line by an antisense approach results in an increase in endogenous tyrosine hydroxylase levels. In contrast, the level of the neuronal marker protein PGP9.5 remains unchanged in the antisense lines whereas that of the neuronal nitric oxide synthase decreases. Hence, the tyrosine hydroxylase gene is a natural target for repression by Oct-2 in neuronal cells. The significance of this effect is discussed in terms of the processes that regulate tyrosine hydroxylase gene expression and the role of Oct-2 in neuronal cells.
POU家族转录因子Oct-2最初是在B淋巴细胞中发现的,但已证明它在神经元细胞中表达,尽管在大多数其他细胞类型中不存在。将Oct-2表达载体与酪氨酸羟化酶启动子/报告质粒共转染到非神经元细胞中表明,在这种人工情况下Oct-2可以抑制该启动子。在此我们报告,通过反义方法降低神经元细胞系中内源性Oct-2水平会导致内源性酪氨酸羟化酶水平升高。相反,在反义细胞系中神经元标记蛋白PGP9.5的水平保持不变,而神经元型一氧化氮合酶的水平降低。因此,酪氨酸羟化酶基因是Oct-2在神经元细胞中抑制的天然靶点。从调节酪氨酸羟化酶基因表达的过程以及Oct-2在神经元细胞中的作用方面讨论了这种效应的意义。