TY - JOUR
T1 - Development of an RNA Virus-Based Episomal Vector Capable of Switching Transgene Expression
AU - Yamamoto, Yusuke
AU - Tomonaga, Keizo
AU - Honda, Tomoyuki
N1 - Funding Information:
Funding. This study was supported in part by JSPS KAKENHI Grant Numbers JP17H04083 (KT), JP19K22530 (KT), JP15K08496 (TH), JP18H02664 (TH), and JP18K19449 (TH); MEXT KAKENHI Grant Numbers JP16H06429 (KT), JP16K21723 (KT), and JP16H06430 (KT); JSPS Core-to-Core Program, AMED Grant Number JP19fm0208014 (KT); grants from the Takeda Science Foundation (TH), The Shimizu Foundation for Immunology and Neuroscience Grant for 2015 (TH); and the Joint Usage/Research Center Program of Institute for Frontier Life and Medical Sciences, Kyoto University.
Publisher Copyright:
© Copyright © 2019 Yamamoto, Tomonaga and Honda.
PY - 2019/11/6
Y1 - 2019/11/6
N2 - Viral vectors are efficient gene delivery systems, although most of these vectors still present limitations to their practical use, such as achieving only transient transgene expression and a risk of insertional mutations. We have recently developed an RNA virus-based episomal vector (REVec), based on nuclear-replicating Borna disease virus (BoDV). REVec can transduce transgenes into various types of cells and stably express transgenes; however, an obstacle to the practical use of REVec is the lack of a mechanism to turn off transgene expression once REVec is transduced. Here, we developed a novel REVec system, REVec-L2b9, in which transgene expression can be switched on and off by using a theophylline-dependent self-cleaving riboswitch. Transgene expression from REVec-L2b9 was suppressed in the absence of theophylline and induced by theophylline administration. Conversely, transgene expression from REVec-L2b9 was switched off by removing theophylline. To our knowledge, REVec-L2b9 is the first nuclear-replicating RNA virus vector capable of switching transgene expression on and off as needed, which will expand the potential for gene therapies by increasing safety and usability.
AB - Viral vectors are efficient gene delivery systems, although most of these vectors still present limitations to their practical use, such as achieving only transient transgene expression and a risk of insertional mutations. We have recently developed an RNA virus-based episomal vector (REVec), based on nuclear-replicating Borna disease virus (BoDV). REVec can transduce transgenes into various types of cells and stably express transgenes; however, an obstacle to the practical use of REVec is the lack of a mechanism to turn off transgene expression once REVec is transduced. Here, we developed a novel REVec system, REVec-L2b9, in which transgene expression can be switched on and off by using a theophylline-dependent self-cleaving riboswitch. Transgene expression from REVec-L2b9 was suppressed in the absence of theophylline and induced by theophylline administration. Conversely, transgene expression from REVec-L2b9 was switched off by removing theophylline. To our knowledge, REVec-L2b9 is the first nuclear-replicating RNA virus vector capable of switching transgene expression on and off as needed, which will expand the potential for gene therapies by increasing safety and usability.
KW - Borna disease virus
KW - expression control
KW - riboswitch
KW - safety
KW - virus vector
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U2 - 10.3389/fmicb.2019.02485
DO - 10.3389/fmicb.2019.02485
M3 - Article
AN - SCOPUS:85075547730
SN - 1664-302X
VL - 10
JO - Frontiers in Microbiology
JF - Frontiers in Microbiology
M1 - 2485
ER -