Literature DB >> 8955060

The herpes simplex virus type 1 UL6 protein is essential for cleavage and packaging but not for genomic inversion.

C Lamberti1, S K Weller.   

Abstract

The HSV-1 genome is composed of two unique regions (UL and US) flanked by inverted repeats. During the course of DNA replication the two unique regions UL and US invert relative to one another. In this report we present evidence that cleavage is not necessary for genomic inversion to occur. We isolated and characterized a UL6::lacZ insertion mutant (hr74) that produces wild-type levels of replicating viral DNA but fails to cleave and package DNA. We demonstrate that this virus is still able to undergo genomic inversion. Furthermore we confirm that replicating DNA from cells infected with wild-type virus contains specific UL terminal but not US termini, whereas cells infected with the mutant hr74 do not contain either US or UL termini. This demonstrates that the specific UL ends found in replicating DNA are the result of the cleavage/packaging process.

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Year:  1996        PMID: 8955060     DOI: 10.1006/viro.1996.0668

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  70 in total

1.  Machinery to support genome segment inversion exists in a herpesvirus which does not naturally contain invertible elements.

Authors:  M A McVoy; D Ramnarain
Journal:  J Virol       Date:  2000-05       Impact factor: 5.103

2.  The ends on herpesvirus DNA replicative concatemers contain pac2 cis cleavage/packaging elements and their formation is controlled by terminal cis sequences.

Authors:  M A McVoy; D E Nixon; J K Hur; S P Adler
Journal:  J Virol       Date:  2000-02       Impact factor: 5.103

3.  DNA cleavage and packaging proteins encoded by genes U(L)28, U(L)15, and U(L)33 of herpes simplex virus type 1 form a complex in infected cells.

Authors:  Philippa M Beard; Naomi S Taus; Joel D Baines
Journal:  J Virol       Date:  2002-05       Impact factor: 5.103

Review 4.  HSV-1-based vectors for gene therapy of neurological diseases and brain tumors: part I. HSV-1 structure, replication and pathogenesis.

Authors:  A Jacobs; X O Breakefield; C Fraefel
Journal:  Neoplasia       Date:  1999-11       Impact factor: 5.715

5.  Identification of small molecule compounds that selectively inhibit varicella-zoster virus replication.

Authors:  Robert J Visalli; Jeanette Fairhurst; Shamala Srinivas; William Hu; Boris Feld; Martin DiGrandi; Kevin Curran; Adma Ross; Jonathan D Bloom; Marja van Zeijl; Thomas R Jones; John O'Connell; Jeffrey I Cohen
Journal:  J Virol       Date:  2003-02       Impact factor: 5.103

6.  Monitoring prevalence of varicella-zoster virus clades in Germany.

Authors:  A Sauerbrei; J Stefanski; A Philipps; A Krumbholz; R Zell; P Wutzler
Journal:  Med Microbiol Immunol       Date:  2010-10-31       Impact factor: 3.402

7.  ICP8 Filament Formation Is Essential for Replication Compartment Formation during Herpes Simplex Virus Infection.

Authors:  Anthar S Darwish; Lorry M Grady; Ping Bai; Sandra K Weller
Journal:  J Virol       Date:  2015-12-16       Impact factor: 5.103

8.  The varicella-zoster virus portal protein is essential for cleavage and packaging of viral DNA.

Authors:  Melissa A Visalli; Brittany L House; Anca Selariu; Hua Zhu; Robert J Visalli
Journal:  J Virol       Date:  2014-05-07       Impact factor: 5.103

9.  The UL6 gene product forms the portal for entry of DNA into the herpes simplex virus capsid.

Authors:  W W Newcomb; R M Juhas; D R Thomsen; F L Homa; A D Burch; S K Weller; J C Brown
Journal:  J Virol       Date:  2001-11       Impact factor: 5.103

10.  The UL7 gene of pseudorabies virus encodes a nonessential structural protein which is involved in virion formation and egress.

Authors:  Walter Fuchs; Harald Granzow; Robert Klopfleisch; Barbara G Klupp; Daniela Rosenkranz; Thomas C Mettenleiter
Journal:  J Virol       Date:  2005-09       Impact factor: 5.103

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