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Transcription of Hepatitis Delta Antigen mRNA Continues throughout Hepatitis Delta Virus (HDV) Replication: a New Model of HDV RNA Transcription and Replication

机译:肝炎三角洲抗原mRNA的转录在整个肝炎三角洲病毒(HDV)复制中持续进行:HDV RNA转录和复制的新模型

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摘要

Hepatitis delta virus (HDV) replicates by RNA-dependent RNA synthesis according to a double rolling circle model. Also synthesized during replication is a 0.8-kb, polyadenylated mRNA encoding the hepatitis delta antigen (HDAg). It has been proposed that this mRNA species represents the initial product of HDV RNA replication; subsequent production of genomic-length HDV RNA relies on suppression of the HDV RNA polyadenylation signal by HDAg. However, this model was based on studies which required the use of an HDV cDNA copy to initiate HDV RNA replication in cell culture, thus introducing an artificial requirement for DNA-dependent RNA synthesis. We have now used an HDV cDNA-free RNA transfection system and a method that we developed to detect specifically the mRNA species transcribed from the HDV RNA template. We established that this polyadenylated mRNA is 0.8 kb in length and its 5′ end begins at nucleotide 1631. Surprisingly, kinetic studies showed that this mRNA continued to be synthesized even late in the viral replication cycle and that the mRNA and the genomic-length RNA increased in parallel, even in the presence of HDAg. Thus, a switch from production of the HDAg mRNA to the full-length HDV RNA does not occur in this system, and suppression of the polyadenylation site by HDAg may not significantly regulate the synthesis of the HDAg mRNA, as previously proposed. These findings reveal novel insights into the mechanism of HDV RNA replication. A new model of HDV RNA replication and transcription is proposed.
机译:肝炎三角洲病毒(HDV)根据双滚环模型通过RNA依赖性RNA合成进行复制。复制期间还合成了一个0.8 kb的聚腺苷酸化mRNA,编码肝炎三角洲抗原(HDAg)。已经提出该mRNA种类代表HDV RNA复制的初始产物。随后产生的基因组长度的HDV RNA依赖于HDAg对HDV RNA聚腺苷酸化信号的抑制。然而,该模型基于研究,该研究需要使用HDV cDNA复制来启动细胞培养中的HDV RNA复制,从而为依赖DNA的RNA合成引入了人工需求。现在,我们已经使用了无HDV cDNA的RNA转染系统,并且开发了一种方法来专门检测从HDV RNA模板转录的mRNA物种。我们确定该多腺苷酸化的mRNA的长度为0.8 kb,其5'末端始于核苷酸1631。令人惊讶的是,动力学研究表明,即使在病毒复制周期的后期,该mRNA仍继续合成,并且该mRNA和基因组长度的RNA即使存在HDAg,其并行增加。因此,在该系统中不会发生从HDAg mRNA的产生到全长HDV RNA的转变,并且如先前所提出的那样,HDAg对多腺苷酸化位点的抑制可能不会显着调节HDAg mRNA的合成。这些发现揭示了对HDV RNA复制机制的新颖见解。提出了一种新的HDV RNA复制和转录模型。

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