Fluorescence imaging to understand the molecular mechanism of DNA damage-triggered cellular reprogramming in plants

We recently found that massive but transient DNA strand breaks, a kind of DNA damage, can trigger cellular reprogramming of differentiated cells to stem cells in the moss Physcomitrella patens (Physcomitrella). In Physcomitrella, DNA is massively damaged by the treatment with a DNA strand break-indu...

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Main Authors Tamada, Yosuke, Imai, Akihiro, Gu, Nan
Format Conference Proceeding
LanguageEnglish
Published SPIE 27.10.2021
Online AccessGet full text
ISBN1510647198
9781510647190
ISSN0277-786X
DOI10.1117/12.2615404

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Abstract We recently found that massive but transient DNA strand breaks, a kind of DNA damage, can trigger cellular reprogramming of differentiated cells to stem cells in the moss Physcomitrella patens (Physcomitrella). In Physcomitrella, DNA is massively damaged by the treatment with a DNA strand break-inducing reagent at high concentration. The DNA damage was repaired within 24 hours after the removal of the reagent. Then, the promoter activity of STEMIN1, encoding an integrator of the reprogramming signals, became active in a part of leaf cells, which eventually became stem cells. Levels of DNA strand breaks were quantified by performing comet assay, where the nuclei are subject to electrophoresis, stained with the fluorescent dye that binds to DNA, and observed with fluorescent microscope. The promoter activity of STEMIN1 was visualized using fluorescent protein and observed with fluorescent microscopy.
AbstractList We recently found that massive but transient DNA strand breaks, a kind of DNA damage, can trigger cellular reprogramming of differentiated cells to stem cells in the moss Physcomitrella patens (Physcomitrella). In Physcomitrella, DNA is massively damaged by the treatment with a DNA strand break-inducing reagent at high concentration. The DNA damage was repaired within 24 hours after the removal of the reagent. Then, the promoter activity of STEMIN1, encoding an integrator of the reprogramming signals, became active in a part of leaf cells, which eventually became stem cells. Levels of DNA strand breaks were quantified by performing comet assay, where the nuclei are subject to electrophoresis, stained with the fluorescent dye that binds to DNA, and observed with fluorescent microscope. The promoter activity of STEMIN1 was visualized using fluorescent protein and observed with fluorescent microscopy.
Author Gu, Nan
Tamada, Yosuke
Imai, Akihiro
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  organization: Hiroshima Institute of Technology (Japan)
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DOI 10.1117/12.2615404
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Editor Aizu, Yoshihisa
Matoba, Osamu
Luo, Yuan
Awatsuji, Yasuhiro
Yatagai, Toyohiko
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  organization: Muroran Institute of Technology (Japan)
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  organization: Kobe Univ. (Japan)
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  organization: Kyoto Institute of Technology (Japan)
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  fullname: Luo, Yuan
  organization: National Taiwan Univ. (Taiwan)
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Conference Date: 2021-04-20|2021-04-22
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Snippet We recently found that massive but transient DNA strand breaks, a kind of DNA damage, can trigger cellular reprogramming of differentiated cells to stem cells...
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Title Fluorescence imaging to understand the molecular mechanism of DNA damage-triggered cellular reprogramming in plants
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