首页> 美国卫生研究院文献>Virology Journal >Repressor element-1 silencing transcription factoreuronal restrictive silencer factor (REST/NRSF) can regulate HSV-1 immediate-early transcription via histone modification
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Repressor element-1 silencing transcription factoreuronal restrictive silencer factor (REST/NRSF) can regulate HSV-1 immediate-early transcription via histone modification

机译:阻遏因子1沉默转录因子/神经元限制性沉默因子(REST / NRSF)可通过组蛋白修饰调控HSV-1立即早期转录

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摘要

BackgroundDuring primary infection of its human host, Herpes Simplex Virus Type-1 (HSV-1) establishes latency in neurons where the viral genome is maintained in a circular form associated with nucleosomes in a chromatin configration. During latency, most viral genes are silenced, although the molecular mechanisms responsible for this are unclear. We hypothesized that neuronal factors repress HSV-1 gene expression during latency. A search of the HSV-1 DNA sequence for potential regulatory elements identified a Repressor Element-1/Neuronal Restrictive Silencer Element (RE-1/NRSE) located between HSV-1 genes ICP22 and ICP4. We predicted that the Repressor Element Silencing Transcription Factor/Neuronal Restrictive Silencer Factor (REST/NRSF) regulates expression of ICP22 and ICP4.
机译:背景在人类宿主的初次感染期间,单纯疱疹病毒1型(HSV-1)在神经元中建立了潜伏期,其中病毒基因组以与染色质构型相关的核小体相关的环状形式维持。在潜伏期,大多数病毒基因被沉默,尽管造成这种现象的分子机制尚不清楚。我们假设神经元因素在潜伏期期间抑制HSV-1基因表达。在HSV-1 DNA序列中寻找潜在的调控元件,确定了位于HSV-1基因ICP22和ICP4之间的阻遏元件1 /神经元限制性沉默元件(RE-1 / NRSE)。我们预测阻遏物沉默转录因子/神经元限制性沉默因子(REST / NRSF)调节ICP22和ICP4的表达。

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