Literature DB >> 11900834

EHV-1 EICP22 protein sequences that mediate its physical interaction with the immediate-early protein are not sufficient to enhance the trans-activation activity of the IE protein.

Wilbert A Derbigny1, Seong K Kim, Hyung K Jang, Dennis J O'Callaghan.   

Abstract

The early 293 amino acid EICP22 protein (EICP22P) of equine herpesvirus 1 localizes within the nucleus and functions as an accessory regulatory protein (J. Virol. 68 (1994) 4329). Transient transfection assays indicated that although the EICP22P by itself only minimally trans-activates EHV-1 promoters, the EICP22P functions synergistically with the immediate-early protein (IEP) to enhance expression of EHV-1 early genes (J. Virol. 71 (1997) 1004). We previously showed that the EICP22 protein enhances the DNA-binding activity of the EHV-1 IEP and that it also physically interacts with the IEP (J. Virol. 74 (2000) 1425). In this communication, we employed transient trans-activation assays utilizing EICP22P deletion mutants to address whether the sequences required for EICP22P-IEP physical interactions are essential for EICP22P's ability to interact synergistically with the IEP. Assays employing various classes of the EHV-1 promoters fused to the chloramphenicol acetyl-transferase (CAT) reporter gene indicated that: (1) neither full length nor any of the EICP22P mutants tested was able to overcome repression of the IE promoter elicited by the IEP, (2) the full-length EICP22P interacted synergistically with the IEP to trans-activate the early and late promoters tested, and (3) all of the EICP22P mutants, including those that were able to physically interact with IEP and itself, failed to function synergistically with the IEP to trans-activate representative EHV-1 early and late promoters. The results suggest that EICP22P sequences required for its interaction with the IE protein are not sufficient to mediate its synergistic effect on the trans-activation function of the IEP. The possible explanations as to why sequences in addition to those that mediate EICP22P-IEP interaction and EICP22P self-interactions are essential for the synergistic function of EICP22P are discussed.

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Year:  2002        PMID: 11900834     DOI: 10.1016/s0168-1702(01)00377-x

Source DB:  PubMed          Journal:  Virus Res        ISSN: 0168-1702            Impact factor:   3.303


  13 in total

1.  Characterization of cis-acting elements required for autorepression of the equine herpesvirus 1 IE gene.

Authors:  Seongman Kim; Gan Dai; Dennis J O'Callaghan; Seong Kee Kim
Journal:  Virus Res       Date:  2012-01-14       Impact factor: 3.303

2.  Biological and genotypic properties of defective interfering particles of equine herpesvirus 1 that mediate persistent infection.

Authors:  Paul D Ebner; Seong K Kim; Dennis J O'Callaghan
Journal:  Virology       Date:  2008-09-20       Impact factor: 3.616

3.  Genetic complexity of EHV-1 defective interfering particles and identification of novel IR4/UL5 hybrid proteins produced during persistent infection.

Authors:  Paul D Ebner; Dennis J O'Callaghan
Journal:  Virus Genes       Date:  2006-06       Impact factor: 2.332

4.  The unique IR2 protein of equine herpesvirus 1 negatively regulates viral gene expression.

Authors:  Seong K Kim; Byung C Ahn; Randy A Albrecht; Dennis J O'Callaghan
Journal:  J Virol       Date:  2006-05       Impact factor: 5.103

5.  The equine herpesvirus-1 IR3 gene that lies antisense to the sole immediate-early (IE) gene is trans-activated by the IE protein, and is poorly expressed to a protein.

Authors:  Byung Chul Ahn; Jonathan E Breitenbach; Seong K Kim; Dennis J O'Callaghan
Journal:  Virology       Date:  2007-02-15       Impact factor: 3.616

6.  The equine herpesvirus-1 (EHV-1) IR3 transcript downregulates expression of the IE gene and the absence of IR3 gene expression alters EHV-1 biological properties and virulence.

Authors:  Byung Chul Ahn; Yunfei Zhang; Dennis J O'Callaghan
Journal:  Virology       Date:  2010-04-24       Impact factor: 3.616

7.  The immediate-early 63 protein of Varicella-Zoster virus: analysis of functional domains required for replication in vitro and for T-cell and skin tropism in the SCIDhu model in vivo.

Authors:  Armin Baiker; Christoph Bagowski; Hideki Ito; Marvin Sommer; Leigh Zerboni; Klaus Fabel; John Hay; William Ruyechan; Ann M Arvin
Journal:  J Virol       Date:  2004-02       Impact factor: 5.103

8.  A negative regulatory element (base pairs -204 to -177) of the EICP0 promoter of equine herpesvirus 1 abolishes the EICP0 protein's trans-activation of its own promoter.

Authors:  Seong K Kim; Randy A Albrecht; Dennis J O'Callaghan
Journal:  J Virol       Date:  2004-11       Impact factor: 5.103

9.  Interaction of the equine herpesvirus 1 EICP0 protein with the immediate-early (IE) protein, TFIIB, and TBP may mediate the antagonism between the IE and EICP0 proteins.

Authors:  Seong K Kim; Hyung K Jang; Randy A Albrecht; Wilbert A Derbigny; Yunfei Zhang; Dennis J O'Callaghan
Journal:  J Virol       Date:  2003-02       Impact factor: 5.103

10.  The IR4 auxiliary regulatory protein expands the in vitro host range of equine herpesvirus 1 and is essential for pathogenesis in the murine model.

Authors:  Jonathan E Breitenbach; Paul D Ebner; Dennis J O'Callaghan
Journal:  Virology       Date:  2008-11-13       Impact factor: 3.616

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