Silencing of episomal transgene expression by plasmid bacterial DNA elements in vivo

We previously demonstrated that sustainable enhanced levels of transgene products could be expressed from a bacterial DNA-free expression cassette either formed from a fragmented plasmid in mouse liver or delivered as a minicircle vector. This suggested that bacterial DNA sequences played a role in...

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Veröffentlicht in:Gene therapy 2004-05, Vol.11 (10), p.856-864
Hauptverfasser: CHEN, Z. Y, HE, C. Y, MEUSE, L, KAY, M. A
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HE, C. Y
MEUSE, L
KAY, M. A
description We previously demonstrated that sustainable enhanced levels of transgene products could be expressed from a bacterial DNA-free expression cassette either formed from a fragmented plasmid in mouse liver or delivered as a minicircle vector. This suggested that bacterial DNA sequences played a role in episomal transgene silencing. To further understand the silencing mechanism, we systematically altered the DNA components in both the expression cassette and the bacterial backbone, and compared the gene expression profiles from mice receiving different DNA forms. In nine vectors tested, animals that received the purified expression cassette alone always expressed persistently higher levels of transgene compared to 2fDNA groups. In contrast, animals that received linearized DNA by a single cut in the bacterial backbone had similar expression profiles to that of intact plasmid groups. All three linear DNAs formed large concatemers and small circles in mouse liver, while ccDNA remained intact. In all groups, the relative amount of vector DNA in liver remained similar. Together, these results further established that the DNA silencing effect was mediated by a covalent linkage of the expression cassette and the bacteria DNA elements.
doi_str_mv 10.1038/sj.gt.3302231
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Cell therapy and gene therapy</subject><subject>Animals</subject><subject>Applied cell therapy and gene therapy</subject><subject>Bacteria</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Concatamers</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA, Bacterial - genetics</subject><subject>Enhancer Elements, Genetic - genetics</subject><subject>Expression vectors</subject><subject>Factor IX - genetics</subject><subject>Factor IX - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene expression</subject><subject>Gene Expression Profiling</subject><subject>Gene Silencing</subject><subject>Gene therapy</subject><subject>Genetic Vectors - genetics</subject><subject>Health. Pharmaceutical industry</subject><subject>Humans</subject><subject>Industrial applications and implications. 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ispartof Gene therapy, 2004-05, Vol.11 (10), p.856-864
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source MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects alpha 1-Antitrypsin - genetics
alpha 1-Antitrypsin - metabolism
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Animals
Applied cell therapy and gene therapy
Bacteria
Biological and medical sciences
Biotechnology
Concatamers
Deoxyribonucleic acid
DNA
DNA, Bacterial - genetics
Enhancer Elements, Genetic - genetics
Expression vectors
Factor IX - genetics
Factor IX - metabolism
Fundamental and applied biological sciences. Psychology
Gene expression
Gene Expression Profiling
Gene Silencing
Gene therapy
Genetic Vectors - genetics
Health. Pharmaceutical industry
Humans
Industrial applications and implications. Economical aspects
Liver
Liver - metabolism
Medical sciences
Mice
Mice, Inbred C57BL
Nucleotide sequence
Plasmids
Promoter Regions, Genetic - genetics
Transfusions. Complications. Transfusion reactions. Cell and gene therapy
Transgenes
title Silencing of episomal transgene expression by plasmid bacterial DNA elements in vivo
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