Literature DB >> 9367384

Cloning and functional characterization of the origin of lytic-phase DNA replication of rat cytomegalovirus.

C Vink1, E Beuken, C A Bruggeman.   

Abstract

A cis-acting sequence within the rat cytomegalovirus (RCMV) genome (oriLyt) that directs initiation of lytic-phase DNA replication is identified in this report. RCMV oriLyt was localized within a 4.3 kb NcoI fragment that is situated immediately upstream of the gene encoding the major DNA-binding protein. The activity of oriLyt was investigated in a transient replication assay, in which the ability of plasmid constructs to promote DNA replication was tested. Replication of oriLyt-containing plasmids was autonomous and resulted in the generation of high-molecular-mass concatemers of head-to-tail-linked plasmid oligomers. oriLyt-mediated replication was found to depend on viral DNA polymerase activity supplied by RCMV infection. The sequence required for oriLyt function was found to reside within a 3.3 kb HincII-NcoI fragment. The RCMV oriLyt sequence is highly complex, containing 23 direct repeats (DRs) and 16 inverted repeats (IRs) of lengths greater than 10 bp. Two of the DRs (DR21 and DR22) are exceptionally large, being 80 and 88 bp in length, respectively. In addition, two sequence elements (of 127 and 120 bp) with dyad symmetry were identified within oriLyt. Although the sequence similarity of RCMV oriLyt with its human cytomegalovirus counterpart is limited, there is a striking resemblance in the overall organization of several IRs and DRs within both sequences.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9367384     DOI: 10.1099/0022-1317-78-11-2963

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  7 in total

1.  A novel bat herpesvirus encodes homologues of major histocompatibility complex classes I and II, C-type lectin, and a unique family of immune-related genes.

Authors:  Huajun Zhang; Shawn Todd; Mary Tachedjian; Jennifer A Barr; Minhua Luo; Meng Yu; Glenn A Marsh; Gary Crameri; Lin-Fa Wang
Journal:  J Virol       Date:  2012-05-23       Impact factor: 5.103

2.  The r144 major histocompatibility complex class I-like gene of rat cytomegalovirus is dispensable for both acute and long-term infection in the immunocompromised host.

Authors:  P S Beisser; J S Kloover; G E Grauls; M J Blok; C A Bruggeman; C Vink
Journal:  J Virol       Date:  2000-01       Impact factor: 5.103

3.  Complete DNA sequence of the rat cytomegalovirus genome.

Authors:  C Vink; E Beuken; C A Bruggeman
Journal:  J Virol       Date:  2000-08       Impact factor: 5.103

4.  Analysis of human cytomegalovirus oriLyt sequence requirements in the context of the viral genome.

Authors:  Eva-Maria Borst; Martin Messerle
Journal:  J Virol       Date:  2005-03       Impact factor: 5.103

5.  Sequence requirements for interaction of human herpesvirus 7 origin binding protein with the origin of lytic replication.

Authors:  L T Krug; N Inoue; P E Pellett
Journal:  J Virol       Date:  2001-04       Impact factor: 5.103

6.  The rat cytomegalovirus R33-encoded G protein-coupled receptor signals in a constitutive fashion.

Authors:  Yvonne K Gruijthuijsen; Paola Casarosa; Suzanne J F Kaptein; Jos L V Broers; Rob Leurs; Cathrien A Bruggeman; Martine J Smit; Cornelis Vink
Journal:  J Virol       Date:  2002-02       Impact factor: 5.103

7.  The r131 gene of rat cytomegalovirus encodes a proinflammatory CC chemokine homolog which is essential for the production of infectious virus in the salivary glands.

Authors:  Suzanne J F Kaptein; Koen W R van Cleef; Yvonne K Gruijthuijsen; Erik V H Beuken; Lieve van Buggenhout; Patrick S Beisser; Frank R M Stassen; Cathrien A Bruggeman; Cornelis Vink
Journal:  Virus Genes       Date:  2004-08       Impact factor: 2.332

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.