Literature DB >> 16497349

Human polyomavirus JCV late leader peptide region contains important regulatory elements.

Ilhan Akan1, Ilker Kudret Sariyer, Renato Biffi, Victoria Palermo, Stefanie Woolridge, Martyn K White, Shohreh Amini, Kamel Khalili, Mahmut Safak.   

Abstract

Transcription is a complex process that relies on the cooperative interaction between sequence-specific factors and the basal transcription machinery. The strength of a promoter depends on upstream or downstream cis-acting DNA elements, which bind transcription factors. In this study, we investigated whether DNA elements located downstream of the JCV late promoter, encompassing the late leader peptide region, which encodes agnoprotein, play regulatory roles in the JCV lytic cycle. For this purpose, the entire coding region of the leader peptide was deleted and the functional consequences of this deletion were analyzed. We found that viral gene expression and replication were drastically reduced. Gene expression also decreased from a leader peptide point mutant but to a lesser extent. This suggested that the leader peptide region of JCV might contain critical cis-acting DNA elements to which transcription factors bind and regulate viral gene expression and replication. We analyzed the entire coding region of the late leader peptide by a footprinting assay and identified three major regions (region I, II and III) that were protected by nuclear proteins. Further investigation of the first two protected regions by band shift assays revealed a new band that appeared in new infection cycles, suggesting that viral infection induces new factors that interact with the late leader peptide region of JCV. Analysis of the effect of the leader peptide region on the promoter activity of JCV by transfection assays demonstrated that this region has a positive and negative effect on the large T antigen (LT-Ag)-mediated activation of the viral early and late promoters, respectively. Furthermore, a partial deletion analysis of the leader peptide region encompassing the protected regions I and II demonstrated a significant down-regulation of viral gene expression and replication. More importantly, these results were similar to that obtained from a complete deletion of the late leader peptide region, indicating the critical importance of these two protected regions in JCV regulation. Altogether, these findings suggest that the late leader peptide region contains important regulatory elements to which transcription factors bind and contribute to the JCV gene regulation and replication.

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Year:  2006        PMID: 16497349     DOI: 10.1016/j.virol.2006.01.025

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  25 in total

1.  Analysis of JC virus DNA replication using a quantitative and high-throughput assay.

Authors:  Jong Shin; Paul J Phelan; Panharith Chhum; Nazym Bashkenova; Sung Yim; Robert Parker; David Gagnon; Ole Gjoerup; Jacques Archambault; Peter A Bullock
Journal:  Virology       Date:  2014-08-24       Impact factor: 3.616

2.  JC virus nucleotides 376-396 are critical for VP1 capsid protein expression.

Authors:  Laura C Ellis; Igor J Koralnik
Journal:  J Neurovirol       Date:  2014-08-21       Impact factor: 2.643

3.  Extinction of Tumor Antigen Expression by SF2/ASF in JCV-Transformed Cells.

Authors:  Elena Uleri; Sarah Beltrami; Jennifer Gordon; Antonina Dolei; Ilker Kudret Sariyer
Journal:  Genes Cancer       Date:  2011-07

4.  Human polyomavirus JC small regulatory agnoprotein forms highly stable dimers and oligomers: implications for their roles in agnoprotein function.

Authors:  A Sami Saribas; Buenafe T Arachea; Martyn K White; Ronald E Viola; Mahmut Safak
Journal:  Virology       Date:  2011-09-13       Impact factor: 3.616

5.  Nuclear magnetic resonance structure revealed that the human polyomavirus JC virus agnoprotein contains an α-helix encompassing the Leu/Ile/Phe-rich domain.

Authors:  Pascale Coric; A Sami Saribas; Magid Abou-Gharbia; Wayne Childers; Martyn K White; Serge Bouaziz; Mahmut Safak
Journal:  J Virol       Date:  2014-03-26       Impact factor: 5.103

6.  Nuclear Magnetic Resonance Structure of the Human Polyoma JC Virus Agnoprotein.

Authors:  Pascale Coric; A Sami Saribas; Magid Abou-Gharbia; Wayne Childers; Jon H Condra; Martyn K White; Mahmut Safak; Serge Bouaziz
Journal:  J Cell Biochem       Date:  2017-05-03       Impact factor: 4.429

7.  Structure-based release analysis of the JC virus agnoprotein regions: A role for the hydrophilic surface of the major alpha helix domain in release.

Authors:  A Sami Saribas; Martyn K White; Mahmut Safak
Journal:  J Cell Physiol       Date:  2017-08-28       Impact factor: 6.384

8.  JC virus agnoprotein enhances large T antigen binding to the origin of viral DNA replication: evidence for its involvement in viral DNA replication.

Authors:  A Sami Saribas; Martyn K White; Mahmut Safak
Journal:  Virology       Date:  2012-07-27       Impact factor: 3.616

9.  Generation and characterization of JCV permissive hybrid cell lines.

Authors:  Ilker K Sariyer; Mahmut Safak; Jennifer Gordon; Kamel Khalili
Journal:  J Virol Methods       Date:  2009-03-04       Impact factor: 2.014

10.  Dephosphorylation of JC virus agnoprotein by protein phosphatase 2A: inhibition by small t antigen.

Authors:  Ilker K Sariyer; Kamel Khalili; Mahmut Safak
Journal:  Virology       Date:  2008-03-18       Impact factor: 3.616

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