Intracellular distribution of the ORF4 gene product of varicella-zoster virus is influenced by the IE62 protein

被引:13
|
作者
Defechereux, P
Debrus, S
Baudoux, L
Schoonbroodt, S
Merville, MP
Rentier, B
Piette, J
机构
[1] UNIV LIEGE,INST PATHOL B23,DEPT MICROBIOL,LAB FUNDAMENTAL VIROL,B-4000 LIEGE,BELGIUM
[2] UNIV LIEGE,INST PATHOL B23,CLIN CHEM LAB,B-4000 LIEGE,BELGIUM
来源
关键词
D O I
10.1099/0022-1317-77-7-1505
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Varicella-zoster virus (VZV) open reading frame 4-encoded protein (IE4) possesses transactivating properties for VZV genes as well as for genes of heterologous viruses, The major regulatory immediate-early protein of VZV (IE62) is a transactivator of VZV gene expression, In transfection assays, IE4 has been shown to enhance activation induced by IE62, To investigate the functional interactions underlying this observation, indirect immunofluorescence studies were undertaken to determine whether IE62 could influence IE4 intracellular localization in transfected cells, In single transfections, IE4 was predominantly found in cytoplasm, In cotransfection with IE62, the IE4 localization pattern was altered, with nuclear staining predominating over cytoplasmic staining, This effect was specific to the IE62 protein since the gene products of ORF63 and ORF61, which are also regulatory proteins, did not influence IE4 distribution, The use of IE62 mutants indicated that IE62 influence is independent of its transactivation function and that the integrity of regions 3 and 4 is required, IE62 remained nuclear whether IE4 was present or not, These observations underline differences in the regulation of gene expression between VZV proteins and their herpes simplex virus type 1 homologues, In infected cells, IE4 was only sometimes found to colocalize with IE62 in nuclei, This observation suggests that when all VZV proteins are present, complex interactions probably occur which could diminish the influence of IE62.
引用
收藏
页码:1505 / 1513
页数:9
相关论文
共 50 条
  • [21] Differentiation of varicella-zoster virus ORF47 protein kinase and IE62 protein binding domains and their contributions to replication in human skin xenografts in the SCID-hu mouse
    Besser, J
    Sommer, MH
    Zerboni, L
    Bagowski, CP
    Ito, H
    Moffat, J
    Ku, CC
    Arvin, AM
    JOURNAL OF VIROLOGY, 2003, 77 (10) : 5964 - 5974
  • [22] Cellular transcription factor YY1 mediates the varicella-zoster virus (VZV) IE62 transcriptional activation
    Khalil, Mohamed I.
    Sommer, Marvin
    Arvin, Ann
    Hay, John
    Ruyechan, William T.
    VIROLOGY, 2014, 449 : 244 - 253
  • [23] Physical and functional interaction between the varicella zoster virus IE63 and IE62 proteins
    Lynch, JM
    Kenyon, TK
    Grose, C
    Hay, J
    Ruyechan, WT
    VIROLOGY, 2002, 302 (01) : 71 - 82
  • [24] THE PRODUCT OF VARICELLA-ZOSTER VIRUS GENE 62 AUTOREGULATES ITS OWN PROMOTER
    DISNEY, GH
    MCKEE, TA
    PRESTON, CM
    EVERETT, RD
    JOURNAL OF GENERAL VIROLOGY, 1990, 71 : 2999 - 3003
  • [25] Physical interaction between two varicella zoster virus gene regulatory proteins, 1E4 and IE62
    Spengler, ML
    Ruyechan, WT
    Hay, J
    VIROLOGY, 2000, 272 (02) : 375 - 381
  • [26] A MAJOR TRANSACTIVATOR OF VARICELLA-ZOSTER VIRUS, THE IMMEDIATE-EARLY PROTEIN IE62, CONTAINS A POTENT N-TERMINAL ACTIVATION DOMAIN
    PERERA, LP
    MOSCA, JD
    RUYECHAN, WT
    HAYWARD, GS
    STRAUS, SE
    HAY, J
    JOURNAL OF VIROLOGY, 1993, 67 (08) : 4474 - 4483
  • [27] The synthesis and immunogenicity of varicella-zoster virus glycoprotein E and immediate-early protein (IE62) expressed in recombinant herpes simplex virus-1
    Lowry, PW
    Koropchak, CM
    Choi, CYH
    Mocarski, ES
    Kern, ER
    Kinchington, PR
    Arvin, AM
    ANTIVIRAL RESEARCH, 1997, 33 (03) : 187 - 200
  • [28] Interactions between varicella-zoster virus IE62 and cellular transcription factor USF in the coordinate activation of genes 28 and 29
    Meier, JL
    Straus, SE
    NEUROLOGY, 1995, 45 (12) : S30 - S32
  • [29] Characterization of a thienylcarboxamide derivative that inhibits the transactivation functions of cytomegalovirus IE2 and varicella zoster virus IE62
    Majima, Ryuichi
    Shindoh, Keiko
    Yamaguchi, Toyofumi
    Inoue, Naoki
    ANTIVIRAL RESEARCH, 2017, 140 : 142 - 150
  • [30] Analysis of the Varicella-Zoster Virus IE62 N-Terminal Acidic Transactivating Domain and Its Interaction with the Human Mediator Complex
    Yamamoto, Shinobu
    Eletsky, Alexander
    Szyperski, Thomas
    Hay, John
    Ruyechan, William T.
    JOURNAL OF VIROLOGY, 2009, 83 (12) : 6300 - 6305