Literature DB >> 9311789

Evidence for a switch in the mode of human papillomavirus type 16 DNA replication during the viral life cycle.

E R Flores1, P F Lambert.   

Abstract

The study of human papillomavirus type 16 (HPV-16) replication has been impaired because of the lack of a cell culture system that stably maintains viral replication. Recently, cervical epithelial cell populations that stably maintain HPV-16 replicons at a copy number of approximately 1,000 per cell were derived from an HPV-16-infected patient (W12 cell clone 20863 [W12-E cells]). We used neutral/neutral and neutral/alkaline two-dimensional gel electrophoretic techniques to characterize HPV-16 DNA replication in these cells. When W12-E cells were maintained in an undifferentiated state mimicking the nonproductive stage of the life cycle, HPV-16 DNA was found to replicate primarily by theta structures in a bidirectional manner. The initiation site of HPV-16 DNA replication was mapped to approximately nucleotide 100, and the termination site was mapped to between nucleotides 3398 and 5990. To study the productive stage of HPV-16 DNA replication, W12-E cells were grown under culture conditions that promote differentiation of epithelial cell types. Under these conditions, where virus-like particles were detected, the mode of viral DNA replication changed from theta structure to what is apparently a rolling circle mode. Additionally, CIN 612-9E cells, which were derived from an HPV-31-infected patient and harbor HPV-31 extrachromosomally, exhibited the same switch in the mode of DNA replication upon induction of differentiation. These data argue that a fundamental switch in the mechanism of viral DNA replication occurs during the life cycle of the papillomavirus.

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Year:  1997        PMID: 9311789      PMCID: PMC192056          DOI: 10.1128/JVI.71.10.7167-7179.1997

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  35 in total

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Authors:  T T Sun; H Green
Journal:  Cell       Date:  1976-12       Impact factor: 41.582

2.  The localization of replication origins on ARS plasmids in S. cerevisiae.

Authors:  B J Brewer; W L Fangman
Journal:  Cell       Date:  1987-11-06       Impact factor: 41.582

3.  Plasmid-like replicative intermediates of the Epstein-Barr virus lytic origin of DNA replication.

Authors:  R Pfüller; W Hammerschmidt
Journal:  J Virol       Date:  1996-06       Impact factor: 5.103

4.  Identification and characterization of oriLyt, a lytic origin of DNA replication of Epstein-Barr virus.

Authors:  W Hammerschmidt; B Sugden
Journal:  Cell       Date:  1988-11-04       Impact factor: 41.582

5.  Terminal differentiation of cultured human epidermal cells.

Authors:  H Green
Journal:  Cell       Date:  1977-06       Impact factor: 41.582

6.  Selective extraction of polyoma DNA from infected mouse cell cultures.

Authors:  B Hirt
Journal:  J Mol Biol       Date:  1967-06-14       Impact factor: 5.469

7.  Two-dimensional gel electrophoretic method for mapping DNA replicons.

Authors:  K A Nawotka; J A Huberman
Journal:  Mol Cell Biol       Date:  1988-04       Impact factor: 4.272

8.  A cis-acting element from the Epstein-Barr viral genome that permits stable replication of recombinant plasmids in latently infected cells.

Authors:  J Yates; N Warren; D Reisman; B Sugden
Journal:  Proc Natl Acad Sci U S A       Date:  1984-06       Impact factor: 11.205

9.  Bovine papilloma virus plasmids replicate randomly in mouse fibroblasts throughout S phase of the cell cycle.

Authors:  D M Gilbert; S N Cohen
Journal:  Cell       Date:  1987-07-03       Impact factor: 41.582

10.  Laboratory production in vivo of infectious human papillomavirus type 11.

Authors:  J W Kreider; M K Howett; A E Leure-Dupree; R J Zaino; J A Weber
Journal:  J Virol       Date:  1987-02       Impact factor: 5.103

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  93 in total

1.  Genetic analysis of cis regulatory elements within the 5' region of the human papillomavirus type 31 upstream regulatory region during different stages of the viral life cycle.

Authors:  Ellora Sen; Jennifer L Bromberg-White; Craig Meyers
Journal:  J Virol       Date:  2002-05       Impact factor: 5.103

2.  Human papillomavirus type 31 E5 protein supports cell cycle progression and activates late viral functions upon epithelial differentiation.

Authors:  Frauke Fehrmann; David J Klumpp; Laimonis A Laimins
Journal:  J Virol       Date:  2003-03       Impact factor: 5.103

3.  The differentiation-specific factor CDP/Cut represses transcription and replication of human papillomaviruses through a conserved silencing element.

Authors:  M J O'Connor; W Stünkel; C H Koh; H Zimmermann; H U Bernard
Journal:  J Virol       Date:  2000-01       Impact factor: 5.103

4.  Deregulation of eIF4E: 4E-BP1 in differentiated human papillomavirus-containing cells leads to high levels of expression of the E7 oncoprotein.

Authors:  Kwang-Jin Oh; Anna Kalinina; No-Hee Park; Srilata Bagchi
Journal:  J Virol       Date:  2006-07       Impact factor: 5.103

Review 5.  The viral etiology of AIDS-associated malignancies.

Authors:  Peter C Angeletti; Luwen Zhang; Charles Wood
Journal:  Adv Pharmacol       Date:  2008

6.  Sequence and recombination analyses of the geminivirus replication initiator protein.

Authors:  T Vadivukarasi; K R Girish; R Usha
Journal:  J Biosci       Date:  2007-01       Impact factor: 1.826

Review 7.  Replication and partitioning of papillomavirus genomes.

Authors:  Alison A McBride
Journal:  Adv Virus Res       Date:  2008       Impact factor: 9.937

8.  Epigenetics of human papillomaviruses.

Authors:  Eric Johannsen; Paul F Lambert
Journal:  Virology       Date:  2013-08-13       Impact factor: 3.616

9.  Induction of the upstream regulatory region of human papillomavirus type 31 by dexamethasone is differentiation dependent.

Authors:  Jennifer L Bromberg-White; Ellora Sen; Samina Alam; Jason M Bodily; Craig Meyers
Journal:  J Virol       Date:  2003-10       Impact factor: 5.103

10.  Human papillomavirus type 31b E1 and E2 transcript expression correlates with vegetative viral genome amplification.

Authors:  M A Ozbun; C Meyers
Journal:  Virology       Date:  1998-09-01       Impact factor: 3.616

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