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Transcriptional activation of Epstein-Barr virus BRLF1 by USF1 and Rta.
Hung, Chen-Chia; Kuo, Chung-Wen; Wang, Wen-Hung; Chang, Tzu-Hsuan; Chang, Pey-Jium; Chang, Li-Kwan; Liu, Shih-Tung.
Afiliação
  • Hung CC; Molecular Genetics Laboratory, Department of Microbiology and Immunology, Chang-Gung University, Kwei-Shan, Taoyuan 33302, Taiwan, ROC.
  • Kuo CW; Molecular Genetics Laboratory, Department of Microbiology and Immunology, Chang-Gung University, Kwei-Shan, Taoyuan 33302, Taiwan, ROC.
  • Wang WH; Molecular Genetics Laboratory, Department of Microbiology and Immunology, Chang-Gung University, Kwei-Shan, Taoyuan 33302, Taiwan, ROC.
  • Chang TH; Molecular Genetics Laboratory, Department of Microbiology and Immunology, Chang-Gung University, Kwei-Shan, Taoyuan 33302, Taiwan, ROC.
  • Chang PJ; Graduate Institute of Clinical Medical Sciences, Chang-Gung University, Kwei-Shan, Taoyuan 33302, Taiwan, ROC.
  • Chang LK; Department of Biochemical Science and Technology, College of Life Science, National Taiwan University, Taipei 10617, Taiwan, ROC.
  • Liu ST; Molecular Genetics Laboratory, Department of Microbiology and Immunology, Chang-Gung University, Kwei-Shan, Taoyuan 33302, Taiwan, ROC.
J Gen Virol ; 96(9): 2855-2866, 2015 Sep.
Article em En | MEDLINE | ID: mdl-26297580
ABSTRACT
During its lytic cycle, Epstein-Barr virus (EBV) expresses Rta, a factor encoded by BRLF1 that activates the transcription of viral lytic genes. We found that upstream stimulating factor (USF) binds to E1, one of the five E boxes located at - 79 in the BRLF1 promoter (Rp), to activate BRLF1 transcription. Furthermore, Rta was shown to interact with USF1 in coimmunoprecipitation and glutathione S-transferase (GST)-pulldown assays, and confocal laser-scanning microscopy further confirmed that these two proteins colocalize in the nucleus. Rta was also found to bind with the E1 sequence in a biotin-labelled E1 probe, but only in the presence of USF1, suggesting that these two proteins likely form a complex on E1. We subsequently constructed p188mSZ, a reporter plasmid that contained the sequence from - 188 to +5 in Rp, within which the Sp1 site and Zta response element were mutated. In EBV-negative Akata cells cotransfected with p188mSZ and plasmids expressing USF1 and Rta, synergistic activation of Rp transcription was observed. However, after mutating the E1 sequence in p188mSZ, USF1 and Rta were no longer able to transactivate Rp, indicating that Rta autoregulates BRLF1 transcription via its interaction with USF1 on E1. This study showed that pUSF1 transfection after EBV lytic induction in P3HR1 cells increases Rta expression, indicating that USF1 activates Rta expression after the virus enters the lytic cycle. Together, these results reveal a novel mechanism by which USF interacts with Rta to promote viral lytic development, and provide additional insight into the viral-host interactions of EBV.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ativação Transcricional / Transativadores / Proteínas Imediatamente Precoces / Herpesvirus Humano 4 / Infecções por Vírus Epstein-Barr / Fatores Estimuladores Upstream Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ativação Transcricional / Transativadores / Proteínas Imediatamente Precoces / Herpesvirus Humano 4 / Infecções por Vírus Epstein-Barr / Fatores Estimuladores Upstream Idioma: En Ano de publicação: 2015 Tipo de documento: Article