RNA Binding Motif Protein RBM45 Regulates Expression of the 11-Kilodalton Protein of Parvovirus B19 through Binding to Novel Intron Splicing Enhancers

Author:

Wang Jianke12ORCID,Ganaie Safder S.2ORCID,Cheng Fang2,Xu Peng2,Ning Kang2,Wang Xiaomei2,Kleiboeker Steve3,Cheng Shipeng1,Qiu Jianming2ORCID

Affiliation:

1. Institute of Special Animal and Plant Sciences, Chinese Academy of Agricultural Sciences, Changchun, Jilin, China

2. Department of Microbiology, Molecular Genetics and Immunology, University of Kansas Medical Center, Kansas City, Kansas, USA

3. Department of Research and Development, Viracor Eurofins Laboratories, Lee’s Summit, Missouri, USA

Abstract

Human parvovirus B19 (B19V) is a human pathogen that causes severe hematological disorders in immunocompromised individuals. B19V infection has a remarkable tropism with respect to human erythroid progenitor cells (EPCs) in human bone marrow and fetal liver. During B19V infection, only one viral precursor mRNA (pre-mRNA) is transcribed by a single promoter of the viral genome and is alternatively spliced and alternatively polyadenylated, a process which plays a key role in expression of viral proteins. Our studies revealed that a cellular RNA binding protein, RBM45, binds to two intron splicing enhancers and is essential for the maturation of the small nonstructural protein 11-kDa-encoding mRNA. The 11-kDa protein plays an important role not only in B19V infection-induced apoptosis but also in viral DNA replication. Thus, the identification of the RBM45 protein and its cognate binding site in B19V pre-mRNA provides a novel target for antiviral development to combat B19V infection-caused severe hematological disorders.

Funder

HHS | NIH | National Institute of Allergy and Infectious Diseases

National Natural Science Foundation of China

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

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