Adenine DNA Methyltransferase M.CviRI Expression Accelerates Apoptosis in Baculovirus-Infected Insect Cells

Yuannan Xia, James L. Van Etten, Peter Dobos, Yuan Yuan Ling, Peter J. Krell

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

The adenine DNA methyltransferase M.CviRI (TGCmA) gene from chlorella virus XZ-6E was cloned into the Autographa californica nuclear polyhedrosis virus (AcMNPV) genome and expressed in Spodoptera frugiperda insect cells under the control of two tandemly arranged viral promoters, the early ETL promoter and the late polyhedrin promoter. M.CviRI activity was first detected at 10 hr p.i and reached a maximum at 48 hr p.i. Viral DNA synthesized in insect cells infected with M.CviRI expressing virus (AcMTRI) was methylated at all TGCA sites. Unexpectedly, AcMTRI-infected cells lysed 48 hr earlier than wild-type AcMNPV-infected cells. Moreover, cellular DNA, but not viral DNA, from AcMTRI-infected cells was degraded to fragment sizes characteristic of apoptosis. These results suggest that M.CviRI methylation influences the onset of viral cytopathic effects and induces an apoptosis-like response.

Original languageEnglish (US)
Pages (from-to)817-824
Number of pages8
JournalVirology
Volume196
Issue number2
DOIs
StatePublished - Jan 1 1993

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Baculoviridae
Methyltransferases
Adenine
Insects
Apoptosis
DNA
Viral DNA
Viral Cytopathogenic Effect
Viruses
Nucleopolyhedrovirus
Chlorella
Spodoptera
Methylation
Genome
Genes

ASJC Scopus subject areas

  • Virology

Cite this

Adenine DNA Methyltransferase M.CviRI Expression Accelerates Apoptosis in Baculovirus-Infected Insect Cells. / Xia, Yuannan; Van Etten, James L.; Dobos, Peter; Ling, Yuan Yuan; Krell, Peter J.

In: Virology, Vol. 196, No. 2, 01.01.1993, p. 817-824.

Research output: Contribution to journalArticle

Xia, Yuannan ; Van Etten, James L. ; Dobos, Peter ; Ling, Yuan Yuan ; Krell, Peter J. / Adenine DNA Methyltransferase M.CviRI Expression Accelerates Apoptosis in Baculovirus-Infected Insect Cells. In: Virology. 1993 ; Vol. 196, No. 2. pp. 817-824.
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