『徳島大学 教育・研究者情報データベース (EDB)』---[学外] /
ID: Pass:

登録内容 (EID=324603)

EID=324603EID:324603, Map:0, LastModified:2017年5月23日(火) 15:59:00, Operator:[大家 隆弘], Avail:TRUE, Censor:承認済, Owner:[竹本 龍也], 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]
招待 (推奨):
審査 (推奨):
カテゴリ (推奨):
共著種別 (推奨):
学究種別 (推奨):
組織 (推奨):
著者 (必須): 1. (英) Hashimoto M (日) (読)
役割 (任意):
貢献度 (任意):
学籍番号 (推奨):
[継承]
2. (英) Yamashita Y (日) (読)
役割 (任意):
貢献度 (任意):
学籍番号 (推奨):
[継承]
3.竹本 龍也 ([徳島大学.先端酵素学研究所.基幹研究部門])
役割 (任意):
貢献度 (任意):
学籍番号 (推奨):
[継承]
題名 (必須): (英) Electroporation of Cas9 protein/sgRNA into early pronuclear zygotes generates non-mosaic mutants in the mouse.  (日)    [継承]
副題 (任意):
要約 (任意): (英) The CRISPR/Cas9 system is a powerful tool for elucidating the roles of genes in a wide variety of organisms including mice. To obtain genetically modified embryos or mice by this method, Cas9 mRNA and sgRNA are usually introduced into zygotes by microinjection or electroporation. However, most mutants generated with this method are genetically mosaic, composed of several types of cells carrying different mutations, which complicates phenotype analysis in founder embryos or mice. To simplify the analysis and to elucidate the roles of genes involved in developmental processes, a method for producing non-mosaic mutants is needed. Here, we established a method for generating non-mosaic mouse mutant embryos. We introduced Cas9 protein and sgRNA into in vitro fertilized (IVF) zygotes by electroporation, which enabled the genome editing to occur before the first replication of the mouse genome. As a result, all of the cells in the mutant carried the same set of mutations. This method solves the problem of mosaicism/allele complexity in founder mutant embryos or mice generated by the CRIPSR/Cas9 system.  (日)    [継承]
キーワード (推奨):
発行所 (推奨):
誌名 (必須): Developmental Biology (Society for Developmental Biology)
(pISSN: 0012-1606, eISSN: 1095-564X)

ISSN (任意): 1095-564X
ISSN: 0012-1606 (pISSN: 0012-1606, eISSN: 1095-564X)
Title: Developmental biology
Title(ISO): Dev Biol
Publisher: Elsevier Inc.
 (NLM Catalog  (Scopus  (CrossRef (Scopus information is found. [need login])
[継承]
[継承]
(必須): 418 [継承]
(必須): 1 [継承]
(必須): 1 9 [継承]
都市 (任意):
年月日 (必須): 西暦 2016年 7月 26日 (平成 28年 7月 26日) [継承]
URL (任意):
DOI (任意): 10.1016/j.ydbio.2016.07.017    (→Scopusで検索) [継承]
PMID (任意): 27474397    (→Scopusで検索) [継承]
CRID (任意):
Scopus (任意):
researchmap (任意):
評価値 (任意):
被引用数 (任意):
指導教員 (推奨):
備考 (任意): 1.(英) Article.ELocationID: 10.1016/j.ydbio.2016.07.017  (日)    [継承]
2.(英) Article.ELocationID: S0012-1606(16)30241-X  (日)    [継承]
3.(英) Article.PublicationTypeList.PublicationType: Journal Article  (日)    [継承]
4.(英) KeywordList.Keyword: CRISPR/Cas9 system  (日)    [継承]
5.(英) KeywordList.Keyword: Cas9 protein  (日)    [継承]
6.(英) KeywordList.Keyword: Electroporation  (日)    [継承]
7.(英) KeywordList.Keyword: Genome editing  (日)    [継承]

標準的な表示

和文冊子 ● M Hashimoto, Y Yamashita and Tatsuya Takemoto : Electroporation of Cas9 protein/sgRNA into early pronuclear zygotes generates non-mosaic mutants in the mouse., Developmental Biology, 418, 1, 1-9, 2016.
欧文冊子 ● M Hashimoto, Y Yamashita and Tatsuya Takemoto : Electroporation of Cas9 protein/sgRNA into early pronuclear zygotes generates non-mosaic mutants in the mouse., Developmental Biology, 418, 1, 1-9, 2016.

関連情報

Number of session users = 2, LA = 2.33, Max(EID) = 467672, Max(EOID) = 1243068.