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Role of two forms of hepatitis delta virus antigen: Evidence for a mechanism of self-limiting genome replication

  • Mei Chao
  • , Sen Yung Hsieh
  • , John Taylor*
  • *此作品的通信作者
  • Fox Chase Cancer Center

研究成果: 期刊稿件文章同行評審

281 引文 斯高帕斯(Scopus)

摘要

The replication of the RNA genome of hepatitis delta virus is greatly facilitated by the presence of the only known virus-coded protein, the delta antigen. Most, if not all, infections are characterized by the presence of two electrophoretic forms of the delta antigen. These forms correspond to polypeptide lengths of 195 and 214 amino acids which are encoded by genomes with different nucleotide sequences. We used cDNA transfections to investigate the functions of these two forms of the delta antigen. We found that only the small form of delta antigen supported hepatitis delta virus genome replication and that the large form acted as a dominant negative repressor of such replication. This inhibition was potent. For example, the amount of genome replication was reduced eightfold when as little as 10% of the delta antigen was present as the large form. One interpretation of our results is that the delta antigen normally functions as part of a multimeric structure. In addition, our data suggest that synthesis of the large form, either during genome replication in cultured cells or even during infection in animals, may suppress delta replication, possibly leading to a self-limiting infection.

原文英語
頁(從 - 到)5066-5069
頁數4
期刊Journal of Virology
64
發行號10
出版狀態已出版 - 1990
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UN SDG

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  1. SDG3 健康與福祉
    SDG3 健康與福祉

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