Regulation of infected-cell-specific protein synthesis in sfiplb-21 cells productively infected with spodoptera frugiperda multicapsid nuclear polyhedrosis virus

Hsiao Sheng Liu, Shan L. Bilimoria

研究成果: Article同行評審

4 引文 斯高帕斯(Scopus)

摘要

In Spodoptera frugiperda (SF IPLB-21) cells productively infected with S. frugiperda multicapsid nuclear polyhedrosis virus (SfMNPV), we observed the synthesis of infected-cell-specific polypeptides (ICSPs) using the protein synthesis inhibitor cycloheximide (CX) and the DAN synthesis inhibitor cytosine arabinoside (Ara-C) in an attempt to assess whether a temporal cascade and viral DNA synthesis are involved in the gene expression program of SfMNPV. Inhibition of protein synthesis with CX at 0 h postinfection resulted in the active synthesis of a group of ICSPs immediately after removal of CX, suggesting that these polypeptides, designated α-ICSP, did not require de novo protein synthesis for their production. A second group of ICSPs (designated β-ICSPs), requiring a prior interval of protein synthesis, was detected when CX was added at later times. A third group of ICSPs also needed an interval of ICSP synthesis, but differed from β-ICSPs in that they required a longer interval of protein synthesis. Moreover, the synthesis of most of these ICSPs also required DNA synthesis, which was demonstrated by addition of Ara-C before and after viral DNA replication; these ICSPs were therefore designated γ-ICSPs. In conclusion, two kinds of regulatory proesses are involved in SfMNPV infection: the first process controls the sequential synthesis of the three ICSP groups, that is α→β→γ; a second process represses the synthesis of ICSP groups, first of the α-ICSPs and subsequently of β-ICSPs. Thus, we propose temporally regulated as well as negative control circuits in SfMNPV gene expression.

原文English
頁(從 - 到)50-54
頁數5
期刊Intervirology
40
發行號1
DOIs
出版狀態Published - 1997

All Science Journal Classification (ASJC) codes

  • 病毒學
  • 傳染性疾病

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