DNA research : an international journal for rapid publication of reports on genes and genomes · 2010
Human artificial chromosome with a conditional centromere for gene delivery and gene expression.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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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
Аннотация
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.
Предметные рубрики MeSH
AnimalsCHO CellsCell LineCentromereChickensChromosomes, Artificial, HumanCricetinaeCricetulusGene ExpressionGene TargetingGene Transfer TechniquesGenetic TherapyGenetic VectorsGreen Fluorescent ProteinsHumansIn Situ Hybridization, FluorescenceOperator Regions, GeneticPlasmidsPolymerase Chain ReactionRecombination, GeneticTetracyclinesTransgenes