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- W2135551821 abstract "Human cytomegalovirus UL103 encodes a tegument protein that is conserved across herpesvirus subgroups. Mutant viruses lacking this gene product exhibit dramatically reduced accumulation of cell-free virus progeny and poor cell-to-cell spread. Given that viral proteins and viral DNA accumulate with normal kinetics in cells infected with mutant virus, UL103 appears to function during the late phase of replication, playing a critical role in egress of capsidless dense bodies and virions. Few dense bodies were observed in the extracellular space in mutant virus-infected cells in the presence or absence of the DNA encapsidation inhibitor 2-bromo-5,6-dichloro-1-(β-d-ribofuranosyl)benzimidazole. Upon reversal of encapsidation inhibition, UL103 had a striking impact on accumulation of cell-free virus, but not on accumulation of cell-associated virus. Thus, UL103 plays a novel and important role during maturation, regulating virus particle and dense body egress from infected cells." @default.
- W2135551821 created "2016-06-24" @default.
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- W2135551821 date "2011-05-15" @default.
- W2135551821 modified "2023-09-27" @default.
- W2135551821 title "Cytomegalovirus UL103 Controls Virion and Dense Body Egress" @default.
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- W2135551821 doi "https://doi.org/10.1128/jvi.01682-10" @default.
- W2135551821 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3126192" @default.
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