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Human Artificial Chromosome with a Conditional Centromere for Gene Delivery and Gene Expression

Human artificial chromosomes (HACs), which carry a fully functional centromere and are maintained as a single-copy episome, are not associated with random mutagenesis and offer greater control over expression of ectopic genes on the HAC. Recently, we generated a HAC with a conditional centromere, wh...

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Autores principales: Iida, Yuichi, Kim, Jung-Hyun, Kazuki, Yasuhiro, Hoshiya, Hidetoshi, Takiguchi, Masato, Hayashi, Masahiro, Erliandri, Indri, Lee, Hee-Sheung, Samoshkin, Alex, Masumoto, Hiroshi, Earnshaw, William C., Kouprina, Natalay, Larionov, Vladimir, Oshimura, Mitsuo
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955713/
https://www.ncbi.nlm.nih.gov/pubmed/20798231
http://dx.doi.org/10.1093/dnares/dsq020
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author Iida, Yuichi
Kim, Jung-Hyun
Kazuki, Yasuhiro
Hoshiya, Hidetoshi
Takiguchi, Masato
Hayashi, Masahiro
Erliandri, Indri
Lee, Hee-Sheung
Samoshkin, Alex
Masumoto, Hiroshi
Earnshaw, William C.
Kouprina, Natalay
Larionov, Vladimir
Oshimura, Mitsuo
author_facet Iida, Yuichi
Kim, Jung-Hyun
Kazuki, Yasuhiro
Hoshiya, Hidetoshi
Takiguchi, Masato
Hayashi, Masahiro
Erliandri, Indri
Lee, Hee-Sheung
Samoshkin, Alex
Masumoto, Hiroshi
Earnshaw, William C.
Kouprina, Natalay
Larionov, Vladimir
Oshimura, Mitsuo
author_sort Iida, Yuichi
collection PubMed
description Human artificial chromosomes (HACs), which carry a fully functional centromere and are maintained as a single-copy episome, are not associated with random mutagenesis and offer greater control over expression of ectopic genes on the HAC. Recently, we generated a HAC with a conditional centromere, which includes the tetracycline operator (tet-O) sequence embedded in the alphoid DNA array. This conditional centromere can be inactivated, loss of the alphoid(tet)(-)(O) (tet-O HAC) by expression of tet-repressor fusion proteins. In this report, we describe adaptation of the tet-O HAC vector for gene delivery and gene expression in human cells. A loxP cassette was inserted into the tet-O HAC by homologous recombination in chicken DT40 cells following a microcell-mediated chromosome transfer (MMCT). The tet-O HAC with the loxP cassette was then transferred into Chinese hamster ovary cells, and EGFP transgene was efficiently and accurately incorporated into the tet-O HAC vector. The EGFP transgene was stably expressed in human cells after transfer via MMCT. Because the transgenes inserted on the tet-O HAC can be eliminated from cells by HAC loss due to centromere inactivation, this HAC vector system provides important novel features and has potential applications for gene expression studies and gene therapy.
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spelling pubmed-29557132010-10-18 Human Artificial Chromosome with a Conditional Centromere for Gene Delivery and Gene Expression Iida, Yuichi Kim, Jung-Hyun Kazuki, Yasuhiro Hoshiya, Hidetoshi Takiguchi, Masato Hayashi, Masahiro Erliandri, Indri Lee, Hee-Sheung Samoshkin, Alex Masumoto, Hiroshi Earnshaw, William C. Kouprina, Natalay Larionov, Vladimir Oshimura, Mitsuo DNA Res Full Papers Human artificial chromosomes (HACs), which carry a fully functional centromere and are maintained as a single-copy episome, are not associated with random mutagenesis and offer greater control over expression of ectopic genes on the HAC. Recently, we generated a HAC with a conditional centromere, which includes the tetracycline operator (tet-O) sequence embedded in the alphoid DNA array. This conditional centromere can be inactivated, loss of the alphoid(tet)(-)(O) (tet-O HAC) by expression of tet-repressor fusion proteins. In this report, we describe adaptation of the tet-O HAC vector for gene delivery and gene expression in human cells. A loxP cassette was inserted into the tet-O HAC by homologous recombination in chicken DT40 cells following a microcell-mediated chromosome transfer (MMCT). The tet-O HAC with the loxP cassette was then transferred into Chinese hamster ovary cells, and EGFP transgene was efficiently and accurately incorporated into the tet-O HAC vector. The EGFP transgene was stably expressed in human cells after transfer via MMCT. Because the transgenes inserted on the tet-O HAC can be eliminated from cells by HAC loss due to centromere inactivation, this HAC vector system provides important novel features and has potential applications for gene expression studies and gene therapy. Oxford University Press 2010-10 2010-08-26 /pmc/articles/PMC2955713/ /pubmed/20798231 http://dx.doi.org/10.1093/dnares/dsq020 Text en © The Author 2010. Published by Oxford University Press on behalf of Kazusa DNA Research Institute. http://creativecommons.org/licenses/by-nc/2.5/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Iida, Yuichi
Kim, Jung-Hyun
Kazuki, Yasuhiro
Hoshiya, Hidetoshi
Takiguchi, Masato
Hayashi, Masahiro
Erliandri, Indri
Lee, Hee-Sheung
Samoshkin, Alex
Masumoto, Hiroshi
Earnshaw, William C.
Kouprina, Natalay
Larionov, Vladimir
Oshimura, Mitsuo
Human Artificial Chromosome with a Conditional Centromere for Gene Delivery and Gene Expression
title Human Artificial Chromosome with a Conditional Centromere for Gene Delivery and Gene Expression
title_full Human Artificial Chromosome with a Conditional Centromere for Gene Delivery and Gene Expression
title_fullStr Human Artificial Chromosome with a Conditional Centromere for Gene Delivery and Gene Expression
title_full_unstemmed Human Artificial Chromosome with a Conditional Centromere for Gene Delivery and Gene Expression
title_short Human Artificial Chromosome with a Conditional Centromere for Gene Delivery and Gene Expression
title_sort human artificial chromosome with a conditional centromere for gene delivery and gene expression
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955713/
https://www.ncbi.nlm.nih.gov/pubmed/20798231
http://dx.doi.org/10.1093/dnares/dsq020
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