Live imaging of protein kinase activities in transgenic mice expressing FRET biosensor
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- Kamioka Yuji
- Department of Pathology and Biology of Diseases, Graduate School of Medicine, Kyoto University Innovative Techno-Hub for Integrated Medical Bio-Imaging, Kyoto University
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- Sumiyama Kenta
- National Institute of Genetics, Division of Population Genetics
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- Mizuno Rei
- Department of Pathology and Biology of Diseases, Graduate School of Medicine, Kyoto University Department of Gastrointestinal Surgery, Graduate School of Medicine, Kyoto University
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- Sakai Yoshiharu
- Department of Gastrointestinal Surgery, Graduate School of Medicine, Kyoto University
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- Hirata Eishu
- Laboratory of Bioimaging and Cell Signaling, Graduate School of Biostudies, Kyoto University
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- Kiyokawa Etsuko
- Department of Pathology and Biology of Diseases, Graduate School of Medicine, Kyoto University
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- Matsuda Michiyuki
- Department of Pathology and Biology of Diseases, Graduate School of Medicine, Kyoto University Laboratory of Bioimaging and Cell Signaling, Graduate School of Biostudies, Kyoto University
書誌事項
- タイトル別名
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- Live Imaging of Protein Kinase Activities in Transgenic Mice Expressing FRET Biosensors
この論文をさがす
抄録
Genetically-encoded biosensors based on the principle of Förster resonance energy transfer (FRET) have been widely used in biology to visualize the spatiotemporal dynamics of signaling molecules. Despite the increasing multitude of these biosensors, their application has been mostly limited to cultured cells with transient biosensor expression, due to particular difficulties in the development of transgenic mice that express FRET biosensors. In this study, we report the efficient generation of transgenic mouse lines expressing heritable and functional biosensors for ERK and PKA. These transgenic mice were created by the cytoplasmic co-injection of Tol2 transposase mRNA and a circular plasmid harbouring Tol2 recombination sites. High expression of the biosensors in a wide range of cell types allowed us to screen newborn mice simply by inspection. Observation of these transgenic mice by two-photon excitation microscopy yielded real-time activity maps of ERK and PKA in various tissues, with greatly improved signal-to-background ratios. Our transgenic mice may be bred into diverse genetic backgrounds; moreover, the protocol we have developed paves the way for the generation of transgenic mice that express other FRET biosensors, with important applications in the characterization of physiological and pathological signal transduction events in addition to drug development and screening.<br>
収録刊行物
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- Cell Structure and Function
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Cell Structure and Function 37 (1), 65-73, 2012
日本細胞生物学会
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詳細情報 詳細情報について
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- CRID
- 1390282679671854976
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- NII論文ID
- 130004137578
- 40019581951
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- NII書誌ID
- AA0060007X
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- COI
- 1:STN:280:DC%2BC38vhtFOluw%3D%3D
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- ISSN
- 13473700
- 03867196
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- NDL書誌ID
- 024272203
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- PubMed
- 22277578
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
- Crossref
- PubMed
- CiNii Articles
- KAKEN
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- 抄録ライセンスフラグ
- 使用不可