Cellular DNA Ligase I Is Recruited to Cytoplasmic Vaccinia Virus Factories and Masks the Role of the Vaccinia Ligase in Viral DNA Replication (DOI:10.1016/j.chom.2009.11.005);Cellular DNA Ligase I Is Recruited to Cytoplasmic Vaccinia Virus Factories and Masks the Role of the Vaccinia Ligase in Viral DNA Replication

Cell Host and Microbe

Volumn 6, Issue 6, 2009, Pages 563-569

  Paran, Nir ^a   De Silva, Frank S ^a   Senkevich, Tatiana G ^a   Moss, Bernard ^a  

^a NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES   (United States)

Author keywords

DNA; MICROBIO

Indexed keywords

CELL DNA; CELL ENZYME; DNA LIGASE I PROTEIN; POLYDEOXYRIBONUCLEOTIDE SYNTHASE; UNCLASSIFIED DRUG; VIRUS DNA; VIRUS RNA;

ARTICLE; CELL DIVISION; CONTROLLED STUDY; CYTOPLASM; DELETION MUTANT; DNA REPLICATION; DNA SYNTHESIS; GENE EXPRESSION; GENE LOSS; GENE SILENCING; GENETIC CORRELATION; HUMAN; HUMAN CELL; NONHUMAN; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN INDUCTION; PROTEIN LOCALIZATION; VACCINIA VIRUS; VIRUS INFECTION; VIRUS REPLICATION;

MUS; POXVIRIDAE; VACCINIA VIRUS;

EID: 74549202241     PISSN: 19313128     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.chom.2010.01.001     Document Type: Erratum

References (36)

1. Applegren N., Hickey R.J., Kleinschmidt A.M., Zhou Q., Coll J., Wills P., Swaby R., Wei Y., Quan J.Y., Lee M.Y., et al. Further characterization of the human cell multiprotein DNA replication complex. J. Cell. Biochem. 59 (1995) 91-107
2. Broyles S.S. A role for ATP hydrolysis in vaccinia virus early gene transcription. J. Biol. Chem. 266 (1991) 15545-15548
3. Chen X., Zhong S., Zhu X., Dziegielewska B., Ellenberger T., Wilson G.M., MacKerell Jr. A.D., and Tomkinson A.E. Rational design of human DNA ligase inhibitors that target cellular DNA replication and repair. Cancer Res. 68 (2008) 3169-3177
4. Colinas R.J., Goebel S.J., Davis S.W., Johnson G.P., Norton E.K., and Paoletti E. A DNA ligase gene in the Copenhagen strain of vaccinia virus is nonessential for viral replication and recombination. Virology 179 (1990) 267-275
5. De Silva F.S., and Moss B. Effects of vaccinia virus uracil DNA glycosylase catalytic site and deoxyuridine triphosphatase deletion mutations individually and together on replication in active and quiescent cells and pathogenesis in mice. Virol. J. 5 (2008) 145
6. De Silva F.S., Lewis W., Berglund P., Koonin E.V., and Moss B. Poxvirus DNA primase. Proc. Natl. Acad. Sci. USA 104 (2007) 18724-18729
7. De Silva F.S., Paran N., and Moss B. Products and substrate/template usage of vaccinia virus DNA primase. Virology 383 (2009) 136-141
8. Earl P.L., Cooper N., Wyatt L.S., Moss B., and Carroll M.W. Preparation of cell cultures and vaccinia virus stocks. In: Ausubel F.M., Brent R., Kingston R.E., Moore D.D., Seidman J.G., Smith J.A., and Struhl K. (Eds). Current Protocols in Molecular Biology (1998), John Wiley and Sons, New York 16.16.11-16.16.13
9. Earl P.L., Moss B., Wyatt L.S., and Carroll M.W. Generation of recombinant vaccinia viruses. In: Ausubel F.M., Brent R., Kingston R.E., Moore D.D., Seidman J.G., Smith J.A., and Struhl K. (Eds). Current Protocols in Molecular Biology (1998), Greene Publishing Associates & Wiley Interscience, New York 16.17.11-16.17.19
10. Ellenberger T., and Tomkinson A.E. Eukaryotic DNA ligases: structural and functional insights. Annu. Rev. Biochem. 77 (2008) 313-338
11. Esteban M., and Holowczak J.A. Replication of vaccinia DNA in mouse L cells. I. In vivo DNA synthesis. Virology 78 (1977) 57-75
12. Iyer L.M., Aravind L., and Koonin E.V. Common origin of four diverse families of large eukaryotic DNA viruses. J. Virol. 75 (2001) 11720-11734
13. Johansson V.M., Miniotis M.F., Hegardt C., Jonsson G., Staaf J., Berntsson P.S., Oredsson S.M., and Alm K. Effect of polyamine deficiency on proteins involved in Okazaki fragment maturation. Cell Biol. Int. 32 (2008) 1467-1477
14. Katsafanas G.C., and Moss B. Colocalization of transcription and translation within cytoplasmic poxvirus factories coordinates viral expression and subjugates host functions. Cell Host Microbe 2 (2007) 221-228
15. Kerr S.M., and Smith G.L. Vaccinia virus encodes a polypeptide with DNA ligase activity. Nucleic Acids Res. 17 (1989) 9039-9050
16. Kerr S.M., and Smith G.L. Vaccinia virus DNA ligase is nonessential for virus replication: recovery of plasmids from virus-infected cells. Virology 180 (1991) 625-632
17. Kerr S.M., Johnston L.H., Odell M., Duncan S.A., Law K.M., and Smith G.L. Vaccinia DNA ligase complements Saccharomyces cerevisiae Cdc9, localizes in cytoplasmic factories and affects virulence and virus sensitivity to DNA damaging agents. EMBO J. 10 (1991) 4343-4350
18. Lasko D.D., Tomkinson A.E., and Lindahl T. Mammalian DNA ligases. Biosynthesis and intracellular localization of DNA ligase I. J. Biol. Chem. 265 (1990) 12618-12622
19. Lin Y.C., Li J., Irwin C.R., Jenkins H., DeLange L., and Evans D.H. Vaccinia virus DNA ligase recruits cellular topoisomerase II to sites of viral replication and assembly. J. Virol. 82 (2008) 5922-5932
20. Lindahl T., and Barnes D.E. Mammalian DNA ligases. Annu. Rev. Biochem. 61 (1992) 251-281
21. Montecucco A., Biamonti G., Savini E., Focher F., Spadari S., and Ciarrocchi G. DNA ligase I gene expression during differentiation and cell proliferation. Nucleic Acids Res. 20 (1992) 6209-6214
22. Montecucco A., Rossi R., Levin D.S., Gary R., Park M.S., Motycka T.A., Ciarrocchi G., Villa A., Biamonti G., and Tomkinson A.E. DNA ligase I is recruited to sites of DNA replication by an interaction with proliferating cell nuclear antigen: identification of a common targeting mechanism for the assembly of replication factories. EMBO J. 17 (1998) 3786-3795
23. Moss B. Poxviridae: the viruses and their replication. In: Knipe D.M., and Howley P.M. (Eds). Fields Virology (2007), Lippincott Williams & Wilkins, Philadelphia 2905-2946
24. Moss B., and De Silva F. Poxvirus DNA replication and human disease. In: DePamphilis M.L. (Ed). DNA Replication and Human Disease (2006), Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY 707-727
25. Moyer R.W., and Graves R.L. The mechanism of cytoplasmic orthopoxvirus DNA replication. Cell 27 (1981) 391-401
26. Muylaert I., and Elias P. Knockdown of DNA ligase IV/XRCC4 by RNA interference inhibits herpes simplex virus type I DNA replication. J. Biol. Chem. 282 (2007) 10865-10872
27. Niimi A., Suka N., Harata M., Kikuchi A., and Mizuno S. Co-localization of chicken DNA topoisomerase IIalpha, but not beta, with sites of DNA replication and possible involvement of a C-terminal region of alpha through its binding to PCNA. Chromosoma 110 (2001) 102-114
28. Olgiati D.D., Pogo B.G., and Dales S. Evidence for RNA linked to nascent DNA in HeLa cells. J. Cell Biol. 68 (1976) 557-566
29. Parks R.J., Winchcombe-Forhan C., DeLange A.M., Xing X., and Evans D.H. DNA ligase gene disruptions can depress viral growth and replication in poxvirus-infected cells. Virus Res. 56 (1998) 135-147
30. Resch W., Weisberg A.S., and Moss B. Vaccinia virus nonstructural protein encoded by the A11R gene is required for formation of the virion membrane. J. Virol. 79 (2005) 6598-6609
31. Sekiguchi J., and Shuman S. Nick sensing by vaccinia virus DNA ligase requires a 5′ phosphate at the nick and occupancy of the adenylate binding site on the enzyme. J. Virol. 71 (1997) 9679-9684
32. Senkevich T.G., Weisberg A., and Moss B. Vaccinia virus E10R protein is associated with the membranes of intracellular mature virions and has a role in morphogenesis. Virology 278 (2000) 244-252
33. Smith G.L., Chan Y.S., and Kerr S.M. Transcriptional mapping and nucleotide sequence of a vaccinia virus gene encoding a polypeptide with extensive homology to DNA ligases. Nucleic Acids Res. 17 (1989) 9051-9062
34. Vitolo B., Lidonnici M.R., Montecucco C., and Montecucco A. A new monoclonal antibody against DNA ligase I is a suitable marker of cell proliferation in cultured cell and tissue section samples. Eur. J. Histochem. 49 (2005) 349-354
35. Walsh D., Arias C., Perez C., Halladin D., Escandon M., Ueda T., Watanabe-Fukunaga R., Fukunaga R., and Mohr I. Eukaryotic translation initiation factor 4F architectural alterations accompany translation initiation factor redistribution in poxvirus-infected cells. Mol. Cell. Biol. 28 (2008) 2648-2658
36. Wang Y.C., Burkhart W.A., Mackey Z.B., Moyer M.B., Ramos W., Husain I., Chen J., Besterman J.M., and Tomkinson A.E. Mammalian DNA ligase II is highly homologous with vaccinia DNA ligase. Identification of the DNA ligase II active site for enzyme-adenylate formation. J. Biol. Chem. 269 (1994) 31923-31928