首页> 美国卫生研究院文献>Journal of Virology >Localization of cis-acting sequences in the latency-related promoter of bovine herpesvirus 1 which are regulated by neuronal cell type factors and immediate-early genes.
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Localization of cis-acting sequences in the latency-related promoter of bovine herpesvirus 1 which are regulated by neuronal cell type factors and immediate-early genes.

机译:顺式作用序列在牛疱疹病毒1潜伏期相关启动子中的定位受神经元细胞类型因子和即刻早期基因调控。

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摘要

Bovine herpesvirus 1 (BHV-1) establishes a latent infection in sensory ganglionic neurons of cattle. During a latent infection, a single latency-related (LR) transcript is expressed. This observation suggested that DNA sequences in the LR promoter are positively regulated by neural cell type factors. The regulation of the LR gene was examined in neural cells as well as nonneural cells in transient assays. A 258-bp XbaI-SphI fragment from the LR promoter cis activated the herpes simplex virus type 1 thymidine kinase promoter in rat pheochromocytoma (PC-12) cells and differentiated human (HCN1A) neurons. In contrast, cis activation was not observed with rat (Rat-2) fibroblasts, undifferentiated HCN1A cells, or bovine turbinate cells. Treatment of PC-12 cells with nerve growth factor increased transcriptional activity of the XbaI-SphI fragment. Exonuclease III footprinting experiments suggested that nuclear factors bind to the XbaI-SphI fragment. The immediate-early genes of BHV-1 trans activated the LR promoter, and DNA sequences 5' to the XbaI-SphI fragment were necessary for maximal stimulation. These results imply that neural-cell-type-specific factors and BHV-1 immediate-early genes positively regulate LR gene expression.
机译:牛疱疹病毒1(BHV-1)在牛的感觉神经节神经元中建立潜在的感染。在潜伏感染期间,表达单个潜伏期相关(LR)转录本。该观察结果表明LR启动子中的DNA序列受神经细胞类型因子正调控。在瞬时测定中,在神经细胞和非神经细胞中检查了LR基因的调节。 LR启动子顺式的258 bp XbaI-SphI片段激活了大鼠嗜铬细胞瘤(PC-12)细胞和分化的人(HCN1A)神经元中的单纯疱疹病毒1型胸苷激酶启动子。相反,在大鼠(Rat-2)成纤维细胞,未分化的HCN1A细胞或牛鼻甲细胞中未观察到顺式激活。用神经生长因子处理PC-12细胞可增加XbaI-SphI片段的转录活性。核酸外切酶III足迹实验表明,核因子与XbaI-SphI片段结合。 BHV-1的立即早期基因反式激活了LR启动子,而XbaI-SphI片段的5'DNA序列对于最大刺激是必需的。这些结果暗示神经细胞类型特异性因子和BHV-1立即早期基因正调控LR基因表达。

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