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 |
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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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Y ; HE, C. Y ; MEUSE, L ; KAY, M. A</creator><creatorcontrib>CHEN, Z. Y ; HE, C. Y ; MEUSE, L ; KAY, M. A</creatorcontrib><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.</description><identifier>ISSN: 0969-7128</identifier><identifier>EISSN: 1476-5462</identifier><identifier>DOI: 10.1038/sj.gt.3302231</identifier><identifier>PMID: 15029228</identifier><language>eng</language><publisher>Basingstoke: Nature Publishing Group</publisher><subject>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</subject><ispartof>Gene therapy, 2004-05, Vol.11 (10), p.856-864</ispartof><rights>2004 INIST-CNRS</rights><rights>COPYRIGHT 2004 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group May 2004</rights><rights>Nature Publishing Group 2004.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c614t-cf4a3e8860bd52b280f018923c78649cd611a75bc2507a0a32faff5129ef8b3f3</citedby><cites>FETCH-LOGICAL-c614t-cf4a3e8860bd52b280f018923c78649cd611a75bc2507a0a32faff5129ef8b3f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27933,27934</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15727379$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15029228$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>CHEN, Z. Y</creatorcontrib><creatorcontrib>HE, C. Y</creatorcontrib><creatorcontrib>MEUSE, L</creatorcontrib><creatorcontrib>KAY, M. A</creatorcontrib><title>Silencing of episomal transgene expression by plasmid bacterial DNA elements in vivo</title><title>Gene therapy</title><addtitle>Gene Ther</addtitle><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.</description><subject>alpha 1-Antitrypsin - genetics</subject><subject>alpha 1-Antitrypsin - metabolism</subject><subject>Anesthesia. Intensive care medicine. Transfusions. 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. Economical aspects</subject><subject>Liver</subject><subject>Liver - metabolism</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Nucleotide sequence</subject><subject>Plasmids</subject><subject>Promoter Regions, Genetic - genetics</subject><subject>Transfusions. Complications. Transfusion reactions. 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Cell therapy and gene therapy</topic><topic>Animals</topic><topic>Applied cell therapy and gene therapy</topic><topic>Bacteria</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Concatamers</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA, Bacterial - genetics</topic><topic>Enhancer Elements, Genetic - genetics</topic><topic>Expression vectors</topic><topic>Factor IX - genetics</topic><topic>Factor IX - metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene expression</topic><topic>Gene Expression Profiling</topic><topic>Gene Silencing</topic><topic>Gene therapy</topic><topic>Genetic Vectors - genetics</topic><topic>Health. Pharmaceutical industry</topic><topic>Humans</topic><topic>Industrial applications and implications. Economical aspects</topic><topic>Liver</topic><topic>Liver - metabolism</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Nucleotide sequence</topic><topic>Plasmids</topic><topic>Promoter Regions, Genetic - genetics</topic><topic>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</topic><topic>Transgenes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CHEN, Z. Y</creatorcontrib><creatorcontrib>HE, C. Y</creatorcontrib><creatorcontrib>MEUSE, L</creatorcontrib><creatorcontrib>KAY, M. 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Y</au><au>HE, C. Y</au><au>MEUSE, L</au><au>KAY, M. A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Silencing of episomal transgene expression by plasmid bacterial DNA elements in vivo</atitle><jtitle>Gene therapy</jtitle><addtitle>Gene Ther</addtitle><date>2004-05-01</date><risdate>2004</risdate><volume>11</volume><issue>10</issue><spage>856</spage><epage>864</epage><pages>856-864</pages><issn>0969-7128</issn><eissn>1476-5462</eissn><abstract>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.</abstract><cop>Basingstoke</cop><pub>Nature Publishing Group</pub><pmid>15029228</pmid><doi>10.1038/sj.gt.3302231</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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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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