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DOI10.1073/pnas.2025546118
Preventing translational inhibition from ribosomal protein insufficiency by a herpes simplex virus-encoded ribosome-associated protein
Vink E.I.; Andrews J.; Duffy C.; Mohr I.
发表日期2021
ISSN0027-8424
卷号118期号:45
英文摘要In addition to being required for protein synthesis, ribosomes and ribosomal proteins (RPs) also regulate messenger RNA translation in uninfected and virus-infected cells. By individually depleting 85 RPs using RNA interference, we found that overall protein synthesis in uninfected primary fibroblasts was more sensitive to RP depletion than those infected with herpes simplex virus-1 (HSV-1). Although representative RP depletion (uL3, uS4, uL5) inhibited protein synthesis in cells infected with two different DNA viruses (human cytomegalovirus, vaccinia virus), HSV-1-infected cell protein synthesis unexpectedly endured and required a single virusencoded gene product, VP22. During individual RP insufficiency, VP22-expressing HSV-1 replicated better than a VP22-deficient variant. Furthermore, VP22 promotes polysome accumulation in virusinfected cells when uL3 or ribosome availability is limiting and cosediments with initiating and elongating ribosomes in infected and uninfected cells. This identifies VP22 as a virus-encoded, ribosome-associated protein that compensates for RP insufficiency to support viral protein synthesis and replication. Moreover, it reveals an unanticipated class of virus-encoded, ribosome-associated effectors that reduce the dependence of protein synthesis upon host RPs and broadly support translation during physiological stress such as infection. © 2021 National Academy of Sciences. All rights reserved.
英文关键词HSV-1 infection; Physiological stress; Ribosomal protein insufficiency; Translational control
语种英语
来源期刊Proceedings of the National Academy of Sciences of the United States of America
文献类型期刊论文
条目标识符http://gcip.llas.ac.cn/handle/2XKMVOVA/238764
作者单位Department of Microbiology, New York University School of Medicine, New York, NY 10016, United States; Department of Biological Sciences, University of Alabama, Tuscaloosa, AL 35401, United States; Laura and Isaac Perlmutter Cancer Institute, New York University School of Medicine, New York, NY 10016, United States
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Vink E.I.,Andrews J.,Duffy C.,et al. Preventing translational inhibition from ribosomal protein insufficiency by a herpes simplex virus-encoded ribosome-associated protein[J],2021,118(45).
APA Vink E.I.,Andrews J.,Duffy C.,&Mohr I..(2021).Preventing translational inhibition from ribosomal protein insufficiency by a herpes simplex virus-encoded ribosome-associated protein.Proceedings of the National Academy of Sciences of the United States of America,118(45).
MLA Vink E.I.,et al."Preventing translational inhibition from ribosomal protein insufficiency by a herpes simplex virus-encoded ribosome-associated protein".Proceedings of the National Academy of Sciences of the United States of America 118.45(2021).
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