Kaposi’s sarcoma-associated herpesvirus terminal repeat regulates inducible lytic gene promoters

Author:

Izumiya Yoshihiro12ORCID,Algalil Adhraa13,Espera Jonna M.1,Miura Hiroki1,Izumiya Chie1,Inagaki Tomoki1,Kumar Ashish1

Affiliation:

1. Department of Dermatology, School of Medicine, University of California Davis, Sacramento, California, USA

2. Department of Biochemistry and Molecular Medicine, School of Medicine, University of California Davis, Sacramento, California, USA

3. Midwestern University College of Dental Medicine, Glendale, Arizona, USA

Abstract

Enhancers are a crucial regulator of differential gene expression programs. Enhancers are the cis-regulatory sequences determining target genes’ spatiotemporal and quantitative expression. Here, we show that Kaposi’s sarcoma-associated herpesvirus (KSHV) terminal repeats fulfill the enhancer definition for KSHV inducible gene promoters. The KSHV enhancer is occupied by latency-associated nuclear antigen (LANA) and its interacting proteins, such as CHD4. Neighboring terminal repeat (TR) fragments to lytic gene promoters drastically enhanced KSHV replication and transcription activator and LANA transcription regulatory functions. This study, thus, proposes a new latency–lytic switch model in which TR accessibility to the KSHV gene promoters regulates viral inducible gene expression.

Funder

HHS | NIH | National Cancer Institute

HHS | NIH | National Institute of Allergy and Infectious Diseases

Publisher

American Society for Microbiology

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