Please use this identifier to cite or link to this item: https://doi.org/10.1038/emi.2016.110
Title: Intracellular localization of Saffold virus Leader (L) protein differs in Vero and HEp-2 cells
Authors: Xu, Y
Victorio, C.B.L 
Ng, Q
Prabakaran, M
Tan, Y.-J 
Chua, K.B
Keywords: 3C protein
Saffold virus leader protein
unclassified drug
viral protein
viral protein
animal cell
Article
cell nucleus
cellular distribution
cytoplasm
fibroblast
HEp 2 cell line
human
human cell
mouse
nerve cell
nonhuman
priority journal
protein expression
protein function
protein localization
Vero cell line
animal
chemistry
Chlorocebus aethiops
fluorescent antibody technique
genetic transfection
genetics
immunology
metabolism
mutation
nucleocytoplasmic transport
protein transport
Theilovirus
tumor cell line
virion
virology
virus genome
Active Transport, Cell Nucleus
Animals
Cell Line, Tumor
Cell Nucleus
Cercopithecus aethiops
Cytoplasm
Fluorescent Antibody Technique
Genome, Viral
Humans
Mutation
Protein Transport
Theilovirus
Transfection
Vero Cells
Viral Proteins
Virion
Issue Date: 2016
Citation: Xu, Y, Victorio, C.B.L, Ng, Q, Prabakaran, M, Tan, Y.-J, Chua, K.B (2016). Intracellular localization of Saffold virus Leader (L) protein differs in Vero and HEp-2 cells. Emerging Microbes and Infections 5 (10) : e109. ScholarBank@NUS Repository. https://doi.org/10.1038/emi.2016.110
Abstract: The Saffold virus (SAFV) genome is translated as a single long polyprotein precursor and co-translationally cleaved to yield 12 separate viral proteins. Little is known about the activities of SAFV proteins although their homologs in other picornaviruses have already been described. To further support research on functions and activities of respective viral proteins, we investigated the spatio-temporal distribution of SAFV proteins in Vero and HEp-2 cells that had been either transfected with plasmids that express individual viral proteins or infected with live SAFV. Our results revealed that, with the exception of the Leader (L) protein, all viral proteins were localized in the cytoplasm at all the time points assayed. The L protein was found in the cytoplasm at an early time point but was subsequently translocated to the nucleus of HEp-2, but not Vero, cells. This was observed in both transfected and infected cells. Further mutational analysis of L protein revealed that Threonine 58 of the Ser/Thr-rich domain of L protein is crucial for protein trafficking between the cytoplasm and nucleus in HEp-2 cells. These findings contribute to a deeper understanding and stimulate investigation of the differetial cellular responses of HEp-2 cells in comparison to other mammalian cell lines during SAFV infection. © 2016 The Author(s).
Source Title: Emerging Microbes and Infections
URI: https://scholarbank.nus.edu.sg/handle/10635/176119
ISSN: 2222-1751
DOI: 10.1038/emi.2016.110
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