MYBBP1A is required for efficient replication and gene expression of herpes simplex virus 1

Author:

Nobe Moeka1,Maruzuru Yuhei123,Takeshima Kosuke123,Koyanagi Naoto123,Kato Akihisa123,Kawaguchi Yasushi1234ORCID

Affiliation:

1. Department of Microbiology and Immunology, Division of Molecular Virology, The Institute of Medical Science The University of Tokyo Tokyo Japan

2. Department of Infectious Disease Control, International Research Center for Infectious Diseases, The Institute of Medical Science The University of Tokyo Tokyo Minato‐ku Japan

3. Research Center for Asian Infectious Diseases, The Institute of Medical Science The University of Tokyo Tokyo Japan

4. Pandemic Preparedness, Infection and Advanced Research Center The University of Tokyo Tokyo Japan

Abstract

AbstractMore than 100 different herpes simplex virus 1 (HSV‐1) genes belong to three major classes, and their expression is coordinately regulated and sequentially ordered in a cascade. This complex HSV‐1 gene expression is thought to be regulated by various viral and host cellular proteins. A host cellular protein, Myb‐binding protein 1A (MYBBP1A), has been reported to be associated with HSV‐1 viral genomes in conjunction with viral and cellular proteins critical for DNA replication, repair, and transcription within infected cells. However, the role(s) of MYBBP1A in HSV‐1 infections remains unclear. In this study, we examined the effects of MYBBP1A depletion on HSV‐1 infection and found that MYBBP1A depletion significantly reduced HSV‐1 replication, as well as the accumulation of several viral proteins. These results suggest that MYBBP1A is an important host cellular factor that contributes to HSV‐1 replication, plausibly by promoting viral gene expression.

Funder

Uehara Memorial Foundation

Takeda Science Foundation

Japan Agency for Medical Research and Development

Japan Science and Technology Agency

Japan Society for the Promotion of Science

Publisher

Wiley

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