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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/83585
d223ac39-6313-4284-b388-0b8693be91b6
Item type 会議発表用資料 / Presentation(1)
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

WEKO 1007068

小畑, 結衣

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木名瀨, 暁理

× 木名瀨, 暁理

WEKO 1007069

木名瀨, 暁理

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秋光, 信佳

× 秋光, 信佳

WEKO 1007070

秋光, 信佳

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横谷, 明徳

× 横谷, 明徳

WEKO 1007071

横谷, 明徳

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Akari, Kinase

× Akari, Kinase

WEKO 1007072

en Akari, Kinase

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Akinari, Yokoya

× Akinari, Yokoya

WEKO 1007073

en Akinari, Yokoya

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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
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Ver.1 2023-05-15 17:25:04.649666
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