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Post-translational Modification of Delta Antigen of Hepatitis D Virus

机译:丁型肝炎病毒Delta抗原的翻译后修饰

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摘要

The hepatitis delta virus (HDV) genome has only one open reading frame, which encodes the viral small delta antigen. After RNA editing, the same open reading frame is extended 19 amino acids at the carboxyl terminus and encodes the large delta antigen. These two viral proteins escort the HDV genome through different cellular compartments for the complicated phases of replication, transcription and, eventually, the formation of progeny virions. To orchestrate these events, the delta antigens have to take distinct cues to traffic to the right compartments and make correct molecular contacts. In eukaryotes, post-translational modification (PTM) is a major mechanism of dictating the multiple functions of a single protein. Multiple PTMs, including phosphorylation, isoprenylation, acetylation, and methylation, have been identified on hepatitis delta antigens. In this chapter we review these PTMs and discuss their functions in regulating and coordinating the life cycle of HDV.
机译:肝炎三角洲病毒(HDV)基因组只有一个开放阅读框,该框架编码病毒小三角洲抗原。 RNA编辑后,相同的开放阅读框在羧基末端延伸了19个氨基酸,并编码较大的δ抗原。这两种病毒蛋白通过不同的细胞区室护送HDV基因组,以进行复杂的复制,转录和最终形成子代病毒体的阶段。为了编排这些事件,δ抗原必须采取不同的线索才能运输到正确的区室并进行正确的分子接触。在真核生物中,翻译后修饰(PTM)是决定单个蛋白质多功能的主要机制。在肝炎三角洲抗原上已鉴定出多种PTM,包括磷酸化,异戊烯基化,乙酰化和甲基化。在本章中,我们将回顾这些PTM,并讨论其在调节和协调HDV生命周期中的功能。

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