Next Article in Journal
How Human Papillomavirus Replication and Immune Evasion Strategies Take Advantage of the Host DNA Damage Repair Machinery
Next Article in Special Issue
DNA Tumor Virus Regulation of Host DNA Methylation and Its Implications for Immune Evasion and Oncogenesis
Previous Article in Journal
Mutations in HPV18 E1^E4 Impact Virus Capsid Assembly, Infectivity Competence, and Maturation
Previous Article in Special Issue
Epigenetic Regulation of Viral Biological Processes

The Influence of E1A C-Terminus on Adenovirus Replicative Cycle

Department of Microbiology, University of Manitoba, 45 Chancellor’s Circle, Buller Building Room 427, Winnipeg MB R3T 2N2, Canada
Department of Medical Microbiology, University of Manitoba, Winnipeg MB R3E 0J9, Canada
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
Viruses 2017, 9(12), 387;
Received: 27 November 2017 / Revised: 15 December 2017 / Accepted: 16 December 2017 / Published: 19 December 2017
(This article belongs to the Special Issue Viral Subversion of Transcriptional Control)
Adenovirus Early 1A proteins (E1A) are crucial for initiation of the viral life cycle after infection. The E1A gene is encoded at the left end of the viral genome and consists of two exons, the first encoding 185 amino acids in the 289 residues adenovirus 5 E1A, while the second exon encodes 104 residues. The second exon-encoded region of E1A is conserved across all E1A isoforms except for the 55 residues protein, which has a unique C-terminus due to a frame shift following splicing into the second exon. This region of E1A contributes to a variety of processes including the regulation of viral and cellular gene expression, immortalization and transformation. Here we evaluated the contributions that different regions of the second exon of E1A make to the viral life cycle using deletion mutants. The region of E1A encoded by the second exon was found to be important for overall virus growth, induction of viral and cellular gene expression, viral genome replication and deregulation of the cell cycle. Efficient viral replication was found to require exon 2 and the nuclear localization signal, as loss of either resulted in severe growth deficiency. Induction of cellular DNA synthesis was also deficient with any deletion of E1A within the C-terminus even if these deletions were outside of conserved region 4. Overall, our study provides the first comprehensive insight into the contributions of the C-terminus of E1A to the replicative fitness of human adenovirus 5 in arrested lung fibroblasts. View Full-Text
Keywords: E1A; C-terminus; adenovirus E1A; C-terminus; adenovirus
Show Figures

Graphical abstract

MDPI and ACS Style

Crisostomo, L.; Soriano, A.M.; Frost, J.R.; Olanubi, O.; Mendez, M.; Pelka, P. The Influence of E1A C-Terminus on Adenovirus Replicative Cycle. Viruses 2017, 9, 387.

AMA Style

Crisostomo L, Soriano AM, Frost JR, Olanubi O, Mendez M, Pelka P. The Influence of E1A C-Terminus on Adenovirus Replicative Cycle. Viruses. 2017; 9(12):387.

Chicago/Turabian Style

Crisostomo, Leandro, Andrea M. Soriano, Jasmine R. Frost, Oladunni Olanubi, Megan Mendez, and Peter Pelka. 2017. "The Influence of E1A C-Terminus on Adenovirus Replicative Cycle" Viruses 9, no. 12: 387.

Find Other Styles
Note that from the first issue of 2016, MDPI journals use article numbers instead of page numbers. See further details here.

Article Access Map by Country/Region

Back to TopTop