| Literature DB >> 19913636 |
Yoshinori Kitagawa1, Min Zhou, Mayu Yamaguchi, Takayuki Komatsu, Kenji Takeuchi, Masae Itoh, Bin Gotoh.
Abstract
M2-2 protein of human metapneumovirus (HMPV) is encoded by one of two overlapping open reading frames within M2 mRNA. The precise function of HMPV M2-2 protein remains unknown. We here examined effect of M2-2 protein on HMPV transcription and replication using a minigenome construct and monitoring luciferase reporter gene expression. The minigenome assays demonstrated that M2-2 protein inhibited both transcription and RNA replication. The inhibitory function of M2-2 protein was completely abrogated by removal of eight or four amino acids from its N- or C-terminus, respectively, demonstrating importance of both short terminal sequences for maintaining its functional structure. Immunoprecipitation experiments revealed interaction of M2-2 protein with L protein, which might be involved in inhibition of HMPV transcription and replication. Prior accumulation of intracellular M2-2 protein severely restrained HMPV from replicating. Thus inherent viral control of the M2-2 gene expression in infected cells seems to be essential for efficient HMPV replication. Copyright 2009 Elsevier Masson SAS. All rights reserved.Entities:
Mesh:
Substances:
Year: 2009 PMID: 19913636 DOI: 10.1016/j.micinf.2009.11.002
Source DB: PubMed Journal: Microbes Infect ISSN: 1286-4579 Impact factor: 2.700