Literature DB >> 11642367

A tale of two HSV-1 helicases: roles of phage and animal virus helicases in DNA replication and recombination.

B Marintcheva1, S K Weller.   

Abstract

Helicases play essential roles in many important biological processes such as DNA replication, repair, recombination, transcription, splicing, and translation. Many bacteriophages and plant and animal viruses encode one or more helicases, and these enzymes have been shown to play many roles in their respective viral life cycles. In this review we concentrate primarily on the roles of helicases in DNA replication and recombination with special emphasis on the bacteriophages T4, T7, and A as model systems. We explore comparisons between these model systems and the herpesviruses--primarily herpes simplex virus. Bacteriophage utilize various pathways of recombination-dependent DNA replication during the replication of their genomes. In fact the study of recombination in the phage systems has greatly enhanced our understanding of the importance of recombination in the replication strategies of bacteria, yeast, and higher eukaryotes. The ability to "restart" the replication process after a replication fork has stalled or has become disrupted for other reasons is a critical feature in the replication of all organisms studied. Phage helicases and other recombination proteins play critical roles in the "restart" process. Parallels between DNA replication and recombination in phage and in the herpesviruses is explored. We and others have proposed that recombination plays an important role in the life cycle of the herpesviruses, and in this review, we discuss models for herpes simplex virus type 1 (HSV-1) DNA replication. HSV-1 encodes two helicases. UL9 binds specifically to the origins of replication and is believed to initiate HSV DNA replication by unwinding at the origin; the heterotrimeric helicase-primase complex, encoded by UL5, UL8, and UL52 genes, is believed to unwind duplex viral DNA at replication forks. Structure-function analyses of UL9 and the helicase-primase are discussed with attention to the roles these proteins might play during HSV replication.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11642367     DOI: 10.1016/s0079-6603(01)70014-1

Source DB:  PubMed          Journal:  Prog Nucleic Acid Res Mol Biol        ISSN: 0079-6603


  25 in total

Review 1.  A case for the extreme antiquity of recombination.

Authors:  Niles Lehman
Journal:  J Mol Evol       Date:  2003-06       Impact factor: 2.395

Review 2.  Procapsid assembly, maturation, nuclear exit: dynamic steps in the production of infectious herpesvirions.

Authors:  Giovanni Cardone; J Bernard Heymann; Naiqian Cheng; Benes L Trus; Alasdair C Steven
Journal:  Adv Exp Med Biol       Date:  2012       Impact factor: 2.622

Review 3.  Understanding helicases as a means of virus control.

Authors:  D N Frick; A M I Lam
Journal:  Curr Pharm Des       Date:  2006       Impact factor: 3.116

4.  DNA binding activity of the herpes simplex virus type 1 origin binding protein, UL9, can be modulated by sequences in the N terminus: correlation between transdominance and DNA binding.

Authors:  Soma Chattopadhyay; Sandra K Weller
Journal:  J Virol       Date:  2006-05       Impact factor: 5.103

5.  Direct interaction between the N- and C-terminal portions of the herpes simplex virus type 1 origin binding protein UL9 implies the formation of a head-to-tail dimer.

Authors:  Soma Chattopadhyay; Sandra K Weller
Journal:  J Virol       Date:  2007-10-17       Impact factor: 5.103

6.  Processing of lagging-strand intermediates in vitro by herpes simplex virus type 1 DNA polymerase.

Authors:  Yali Zhu; Zetang Wu; M Cristina Cardoso; Deborah S Parris
Journal:  J Virol       Date:  2010-05-05       Impact factor: 5.103

7.  Mutations in the putative zinc-binding motif of UL52 demonstrate a complex interdependence between the UL5 and UL52 subunits of the human herpes simplex virus type 1 helicase/primase complex.

Authors:  Yan Chen; Stacy D Carrington-Lawrence; Ping Bai; Sandra K Weller
Journal:  J Virol       Date:  2005-07       Impact factor: 5.103

Review 8.  Helicases as antiviral drug targets.

Authors:  David N Frick
Journal:  Drug News Perspect       Date:  2003 Jul-Aug

9.  Recruitment of cellular recombination and repair proteins to sites of herpes simplex virus type 1 DNA replication is dependent on the composition of viral proteins within prereplicative sites and correlates with the induction of the DNA damage response.

Authors:  Dianna E Wilkinson; Sandra K Weller
Journal:  J Virol       Date:  2004-05       Impact factor: 5.103

10.  Existence of transdominant and potentiating mutants of UL9, the herpes simplex virus type 1 origin-binding protein, suggests that levels of UL9 protein may be regulated during infection.

Authors:  Boriana Marintcheva; Sandra K Weller
Journal:  J Virol       Date:  2003-09       Impact factor: 5.103

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.