首页> 外文期刊>Archives of virology >Number of and distance between response elements in Kaposi's sarcoma-associated herpesvirus ORF57 promoter influence its activation by replication and transcription activator and its repression by interferon regulatory factor 7.
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Number of and distance between response elements in Kaposi's sarcoma-associated herpesvirus ORF57 promoter influence its activation by replication and transcription activator and its repression by interferon regulatory factor 7.

机译:Kaposi的肉瘤相关Herpesvirus orf57启动子的响应元素之间的数量和距离影响其通过复制和转录激活剂的激活及其受干扰素调节因子7的抑制。

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摘要

Kaposi's sarcoma-associated herpesvirus ORF57 expression is highly responsive to replication and transcription activator (RTA) and interferon regulatory factor 7 (IRF-7). Three RTA response elements (RREs) have been identified in the ORF57 promoter. Here, we show evidence of another functional RRE located between nt 82003 and 82081, which can complement the loss of RTA activation resulting from RRE1 deletion. Repeats of a recombination signal-binding protein Jkappa (RBP-Jkappa) site enhanced RTA activation, which could not be suppressed by IRF-7. Alteration of the distance between the RBP-Jkappa site and RRE2 modulated responsiveness to RTA and IRF-7. These results will help to elucidate the precise regulation of viral gene expression.
机译:Kaposi的肉瘤相关的Herpesvirus Orf57表达对复制和转录激活剂(RTA)和干扰素调节因子7(IRF-7)非常敏感。 在ORF57启动子中鉴定了三个RTA响应元件(RRE)。 在这里,我们显示了位于NT 82003和82081之间的另一个功能RRE的证据,这可以补充RRE1缺失所产生的RTA活化的损失。 重组信号结合蛋白JKAPPA(RBP-JKAPPA)站点的重复增强RTA激活,其无法通过IRF-7抑制。 改变RBP-JKAPPA站点与RRE2调制响应性与RTA和IRF-7之间的距离。 这些结果将有助于阐明病毒基因表达的精确调节。

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