Gene disruption of medaka (Oryzias latipes) orthologue for mammalian tissue-type transglutaminase (TG2) causes movement retardation
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<jats:title>Abstract</jats:title> <jats:p>Transglutaminases are an enzyme family that catalyses protein cross-linking essential for several biological functions. In the previous studies, we characterized the orthologues of the mammalian transglutaminase family in medaka (Oryzias latipes), an established fish model. Among the human isozymes, tissue-type transglutaminase (TG2) has multiple functions that are involved in several biological phenomena. In this study, we established medaka mutants deficient for the orthologue of human TG2 using the CRISPR/Cas9 and transcription activator-like effector nucleases systems. Although apparent morphological changes in the phenotype were not observed, movement retardation was found in the mutant fish when evaluated by a tank-diving test. Furthermore, comparative immunohistochemistry analysis using in this fish model revealed that orthologue of human TG2 was expressed at the periventricular layer of the optic tectum. Our findings provide novel insight for the relationship between tissue-type transglutaminase and the nervous system and the associated behaviour.</jats:p>
収録刊行物
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- The journal of biochemistry
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The journal of biochemistry 168 (3), 213-222, 2020-09
Tokyo : Japanese Biochemical Society
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詳細情報 詳細情報について
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- CRID
- 1522262179746705280
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- NII論文ID
- 40022375409
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- NII書誌ID
- AA00694073
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- ISSN
- 0021924X
- 17562651
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- NDL書誌ID
- 030687152
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- 本文言語コード
- en
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- NDL 雑誌分類
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- ZR2(科学技術--生物学--生化学)
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- データソース種別
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- NDL
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