Zopf D, Dineva B, Betz H, Gundelfinger E D
ZMBH, Universität Heidelberg, FRG.
Nucleic Acids Res. 1990 Feb 11;18(3):521-9. doi: 10.1093/nar/18.3.521.
We have isolated and sequenced genomic DNA clones covering the coding region of the chicken mid-size neurofilament (NF-M) gene and greater than 1 kb of its 5' upstream region. The NF-M gene contains two introns which both are located within the highly conserved C-terminal region of the rod domain. The 5' end of the corresponding mRNA was assigned to a G residue 40 nucleotides upstream of the translation start site and in appropriate distance from a potential TATA box. To functionally analyze the NF-M promoter, constructs carrying 112, 222, and 1026 nucleotides of the 5' upstream region in front of a luciferase reporter gene were tested for their capability to direct luciferase expression after transient transfection into various cell lines. Significant luciferase activity was recorded both in rat phaeochromocytoma (PC12) cells and murine fibroblasts. In PC12 cells, in which neurite outgrowth is induced by nerve growth factor (NGF), expression was stimulated up to 13-fold within 3 days of NGF treatment. This closely resembles expression of the endogenous NF-M gene in response to this hormone.
我们已分离并测序了覆盖鸡中型神经丝(NF-M)基因编码区及其5'上游区域超过1 kb的基因组DNA克隆。NF-M基因包含两个内含子,它们都位于杆状结构域高度保守的C末端区域内。相应mRNA的5'端位于翻译起始位点上游40个核苷酸处的一个G残基,且与潜在的TATA盒保持适当距离。为了对NF-M启动子进行功能分析,测试了在荧光素酶报告基因前携带5'上游区域112、222和1026个核苷酸的构建体在瞬时转染到各种细胞系后指导荧光素酶表达的能力。在大鼠嗜铬细胞瘤(PC12)细胞和小鼠成纤维细胞中均记录到显著的荧光素酶活性。在经神经生长因子(NGF)诱导神经突生长的PC12细胞中,NGF处理3天内表达被刺激高达13倍。这与内源性NF-M基因对该激素的反应表达非常相似。