丁型肝炎病毒小抗原与elav样蛋白HuR的体内相互作用

The Open Virology Journal Pub Date : 2011-01-01 Epub Date: 2011-03-24 DOI:10.2174/1874357901105010012
Ana Casaca, Margarida Fardilha, Edgar da Cruz E Silva, Celso Cunha
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引用次数: 3

摘要

小型和大型δ抗原(分别为S-HDAg和L-HDAg)代表了丁型肝炎病毒(HDV) RNA基因组编码的唯一蛋白质的两种形式。因此,HDV在很大程度上依赖于宿主细胞机制进行复制和转录。到目前为止,只有有限数量的细胞蛋白被确定为参与病毒生命周期调节的S-HDAg或L-HDAg伴侣。为了鉴定细胞s - hdag结合蛋白,我们使用酵母双杂交方法筛选人肝脏cDNA文库。我们能够在体外和体内鉴定出HuR,一种参与RNA稳定的无处不在的表达蛋白,作为S-HDAg的伴侣。在人肝癌细胞中发现HuR与HDAg过表达和共定位。siRNA敲低HuR mRNA可抑制S-HDAg和L-HDAg的表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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In Vivo Interaction of the Hepatitis Delta Virus Small Antigen with the ELAV-Like Protein HuR.

The small and large delta antigens (S-HDAg and L-HDAg, respectively) represent two forms of the only protein encoded by the hepatitis delta virus (HDV) RNA genome. Consequently, HDV relies, at a large extent, on the host cell machinery for replication and transcription. Until now, only a limited number of cellular proteins were identified as S-HDAg or L-HDAg partners being involved in the modulation of the virus life cycle. In an attempt to identify cellular S-HDAg-binding proteins we made use of a yeast two-hybrid approach to screen a human liver cDNA library. We were able to identify HuR, a ubiquitously expressed protein involved in RNA stabilization, as an S-HDAg partner both in vitro and in vivo. HuR was found to be overexpressed and colocalize with HDAg in human hepatoma cells. siRNA knockdown of HuR mRNA resulted in inhibition of S-HDAg and L-HDAg expression.

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