DNA Topoisomerase 1 Facilitates the Transcription and Replication of the Ebola Virus Genome

Author:

Takahashi Kei1,Halfmann Peter2,Oyama Masaaki3,Kozuka-Hata Hiroko3,Noda Takeshi1,Kawaoka Yoshihiro124

Affiliation:

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

2. Influenza Research Institute, Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin—Madison, Madison, Wisconsin, USA

3. Medical Proteomics Laboratory, Institute of Medical Science, University of Tokyo, Tokyo, Japan

4. ERATO Infection-Induced Host Responses Project, Japan Science and Technology Agency, Saitama, Japan

Abstract

ABSTRACT Ebola virus (EBOV) protein L (EBOL) acts as a viral RNA-dependent RNA polymerase. To better understand the mechanisms underlying the transcription and replication of the EBOV genome, we sought to identify cellular factors involved in these processes via their coimmunoprecipitation with EBOL and by mass spectrometry. Of 65 candidate proteins identified, we focused on DNA topoisomerase 1 (TOP1), which localizes to the nucleus and unwinds helical DNA. We found that in the presence of EBOL, TOP1 colocalizes and interacts with EBOL in the cytoplasm, where transcription and replication of the EBOV genome occur. Knockdown of TOP1 markedly reduced virus replication and viral polymerase activity. We also found that the phosphodiester bridge-cleaving and recombination activities of TOP1 are required for the polymerase activity of EBOL. These results demonstrate that TOP1 is an important cellular factor for the transcription and replication of the EBOV genome and, as such, plays a key role in the EBOV life cycle.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

Reference41 articles.

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