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Transfection efficiency depending on distance between a double-strand break site and EGFP-gene in plasmid DNA
https://repo.qst.go.jp/records/83585
https://repo.qst.go.jp/records/83585d223ac39-6313-4284-b388-0b8693be91b6
Item type | 会議発表用資料 / Presentation(1) | |||||
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公開日 | 2021-09-17 | |||||
タイトル | ||||||
タイトル | Transfection efficiency depending on distance between a double-strand break site and EGFP-gene in plasmid DNA | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_c94f | |||||
資源タイプ | conference object | |||||
アクセス権 | ||||||
アクセス権 | metadata only access | |||||
アクセス権URI | http://purl.org/coar/access_right/c_14cb | |||||
著者 |
小畑, 結衣
× 小畑, 結衣× 木名瀨, 暁理× 秋光, 信佳× 横谷, 明徳× Akari, Kinase× Akinari, Yokoya |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | We have established an experimental procedure of transfection and expression of irradiated plasmid DNA encoding fluorescent protein, EGFP, in eukaryotic cells. In this assay, the number of cells expressing the fluorescent protein increases with the incubation of cells as DNA damage is repaired. When a DSB-induced linear plasmid DNA arises after irradiation, it has been thought that the plasmid could be enzymatically digested immediately after transfection or delivery into nucleus. Previously we found that the linear plasmid DNA obtained by restriction enzyme treatments shows slightly expresses EGFP [1]. However, it has not yet been clarified how the linear DNA expresses after transfection. In this study, we aim to elucidate the efficiency of the linear plasmid DNA expression of EGFP in human cells. The linear plasmids were prepared by treatments with various restriction enzymes with different recognition sequences. We cleaved the plasmid around the EGFP gene with three blunt end restriction enzymes at the upstream side, the downstream side, and a 1.2 kbp distance away from the downstream sides of the EGFP gene. Preliminary results indicate that EGFP-expressing was observed for the linear plasmid transfections. The farther the cleavage site from the EGFP gene induced the higher transfection efficiency, suggesting that the plasmids might progressively be digested from the unstable terminal ends when they are transfected into cells. [1] Obata et al. Rad. Res. (2021) In press. | |||||
会議概要(会議名, 開催地, 会期, 主催者等) | ||||||
内容記述タイプ | Other | |||||
内容記述 | 日本放射線影響学会第64回大会 | |||||
発表年月日 | ||||||
日付 | 2021-09-22 | |||||
日付タイプ | Issued |