Literature DB >> 11509884

Murine cytomegalovirus infection induces cellular folylpolyglutamate synthetase activity in quiescent cells.

R Cavallo1, D Lembo, G Gribaudo, S Landolfo.   

Abstract

Cytomegalovirus (CMV) infection stimulates the expression of cellular enzymes involved in the biosynthesis of DNA precursors. Among them, dihydrofolate reductase (DHFR) and thymidylate synthase (TS) require folate as coenzymes. In growing cells, folates are readily converted to polyglutamated forms by the cellular enzyme folylpolyglutamate synthetase (FPGS). Polyglutamated folates are selectively retained within the cell and have an increased affinity for DHFR and TS. Here we report that murine CMV (MCMV) increases the levels of the FPGS mRNAs as well as the enzymatically active FPGS protein through a mechanism that requires viral gene expression. FPGS induction by MCMV would provide the necessary supply of polyglutamated folates to the cellular enzymes involved in the biosynthesis of deoxyribonucleotides, enabling viral DNA replication to take place in quiescent cells. Copyright 2001 S. Karger AG, Basel

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Year:  2001        PMID: 11509884     DOI: 10.1159/000050051

Source DB:  PubMed          Journal:  Intervirology        ISSN: 0300-5526            Impact factor:   1.763


  2 in total

1.  Cell cycle-independent expression of immediate-early gene 3 results in G1 and G2 arrest in murine cytomegalovirus-infected cells.

Authors:  Lüder Wiebusch; Anke Neuwirth; Linus Grabenhenrich; Sebastian Voigt; Christian Hagemeier
Journal:  J Virol       Date:  2008-07-30       Impact factor: 5.103

2.  The ribonucleotide reductase R1 homolog of murine cytomegalovirus is not a functional enzyme subunit but is required for pathogenesis.

Authors:  David Lembo; Manuela Donalisio; Anders Hofer; Maura Cornaglia; Wolfram Brune; Ulrich Koszinowski; Lars Thelander; Santo Landolfo
Journal:  J Virol       Date:  2004-04       Impact factor: 5.103

  2 in total

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