『徳島大学 教育・研究者情報データベース (EDB)』---[学外] /
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登録内容 (EID=348363)

EID=348363EID:348363, Map:0, LastModified:2018年12月10日(月) 11:36:17, Operator:[三木 ちひろ], Avail:TRUE, Censor:0, Owner:[沢津橋 俊], Read:継承, Write:継承, Delete:継承.
種別 (必須): 学術論文 (審査論文) [継承]
言語 (必須): 英語 [継承]
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著者 (必須): 1.沢津橋 俊 ([徳島大学.先端酵素学研究所.基幹研究部門])
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2. (英) Joko Yudai (日) 上甲 裕大 (読) じょうこう ゆうだい
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学籍番号 (推奨): **** [ユーザ]
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3.福本 誠二 ([徳島大学.先端酵素学研究所.基幹研究部門])
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4.松本 俊夫
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5. (英) Sugano S. Shigeo (日) (読)
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題名 (必須): (英) Development of versatile non-homologous end joining-based knock-in module for genome editing.  (日)    [継承]
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要約 (任意): (英) CRISPR/Cas9-based genome editing has dramatically accelerated genome engineering. An important aspect of genome engineering is efficient knock-in technology. For improved knock-in efficiency, the non-homologous end joining (NHEJ) repair pathway has been used over the homology-dependent repair pathway, but there remains a need to reduce the complexity of the preparation of donor vectors. We developed the versatile NHEJ-based knock-in module for genome editing (VIKING). Using the consensus sequence of the time-honored pUC vector to cut donor vectors, any vector with a pUC backbone could be used as the donor vector without customization. Conditions required to minimize random integration rates of the donor vector were also investigated. We attempted to isolate null lines of the VDR gene in human HaCaT keratinocytes using knock-in/knock-out with a selection marker cassette, and found 75% of clones isolated were successfully knocked-in. Although HaCaT cells have hypotetraploid genome composition, the results suggest multiple clones have VDR null phenotypes. VIKING modules enabled highly efficient knock-in of any vectors harboring pUC vectors. Users now can insert various existing vectors into an arbitrary locus in the genome. VIKING will contribute to low-cost genome engineering.  (日)    [継承]
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誌名 (必須): Scientific Reports ([Nature Publishing Group])
(eISSN: 2045-2322)

ISSN (任意): 2045-2322
ISSN: 2045-2322 (eISSN: 2045-2322)
Title: Scientific reports
Title(ISO): Sci Rep
Publisher: Nature Publishing Group
 (NLM Catalog  (Scopus  (CrossRef (Scopus information is found. [need login])
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(必須): 593 593 [継承]
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年月日 (必須): 西暦 2018年 1月 12日 (平成 30年 1月 12日) [継承]
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DOI (任意): 10.1038/s41598-017-18911-9    (→Scopusで検索) [継承]
PMID (任意): 29330493    (→Scopusで検索) [継承]
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Scopus (任意): 2-s2.0-85043529637 [継承]
機関リポジトリ : 112400 [継承]
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備考 (任意): 1.(英) Article.ELocationID: 10.1038/s41598-017-18911-9  (日)    [継承]
2.(英) Article.PublicationTypeList.PublicationType: Journal Article  (日)    [継承]

標準的な表示

和文冊子 ● Shun Sawatsubashi, Yudai Joko, Seiji Fukumoto, Toshio Matsumoto and Shigeo S. Sugano : Development of versatile non-homologous end joining-based knock-in module for genome editing., Scientific Reports, Vol.8, No.1, 593, 2018.
欧文冊子 ● Shun Sawatsubashi, Yudai Joko, Seiji Fukumoto, Toshio Matsumoto and Shigeo S. Sugano : Development of versatile non-homologous end joining-based knock-in module for genome editing., Scientific Reports, Vol.8, No.1, 593, 2018.

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