Genome-Wide Transcriptional Roles of KSHV Viral Interferon Regulatory Factors in Oral Epithelial Cells

Author:

Jang Seung Jin1,Atyeo Natalie1,Mietzsch Mario2ORCID,Chae Min Y.1,McKenna Robert2ORCID,Toth Zsolt134ORCID,Papp Bernadett13456ORCID

Affiliation:

1. Department of Oral Biology, University of Florida College of Dentistry, 1395 Center Drive, Gainesville, FL 32610, USA

2. Department of Biochemistry and Molecular Biology, University of Florida College of Medicine, 1200 Newell Drive, Gainesville, FL 32610, USA

3. UF Genetics Institute, Gainesville, FL 32610, USA

4. UF Health Cancer Center, Gainesville, FL 32610, USA

5. UF Center for Orphaned Autoimmune Disorders, Gainesville, FL 32610, USA

6. UF Informatics Institute, Gainesville, FL 32610, USA

Abstract

The viral interferon regulatory factors (vIRFs) of KSHV are known to dysregulate cell signaling pathways to promote viral oncogenesis and to block antiviral immune responses to facilitate infection. However, it remains unknown to what extent each vIRF plays a role in gene regulation. To address this, we performed a comparative analysis of the protein structures and gene regulation of the four vIRFs. Our structure prediction analysis revealed that despite their low amino acid sequence similarity, vIRFs exhibit high structural homology in both their DNA-binding domain (DBD) and IRF association domain. However, despite this shared structural homology, we demonstrate that each vIRF regulates a distinct set of KSHV gene promoters and human genes in epithelial cells. We also found that the DBD of vIRF1 is essential in regulating the expression of its target genes. We propose that the structurally similar vIRFs evolved to possess specialized transcriptional functions to regulate specific genes.

Funder

National Institutes of Health

NIH/NIDCR

AADOCR

Publisher

MDPI AG

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