Abstract
The nuclear envelope (NE) is a double membrane that segregates nuclear components from the cytoplasm in eukaryotic cells. It is well-known that the NE undergoes a breakdown and reformation during mitosis in animal cells. However, the detailed mechanisms of the NE dynamics are not yet fully understood. Here, we propose a method for the fluorescent labeling of the NE in living cells, which enables the tracing of the NE dynamics during cell division under physiological conditions. In our method, labeling of the NE is accomplished by fixing green fluorescent protein carrying the nuclear localization signal on the inner nuclear membrane based on a unique biotinylation reaction from the archaeon Sulfolobus tokodaii. With this method, we observed HeLa cells during mitosis by confocal laser scanning microscopy and succeeded in clearly visualizing the difference in the timing of the formation of the NE and the nuclear lamina.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Acetyl-CoA Carboxylase / genetics
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Acetyl-CoA Carboxylase / metabolism
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Archaeal Proteins / genetics
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Archaeal Proteins / metabolism
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Biotin / metabolism
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Biotinylation
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Carbon-Nitrogen Ligases / genetics
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Carbon-Nitrogen Ligases / metabolism
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Fatty Acid Synthase, Type II / genetics
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Fatty Acid Synthase, Type II / metabolism
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Fluorescence
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Fluorescent Dyes / chemistry
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Fluorescent Dyes / metabolism*
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Green Fluorescent Proteins / chemistry
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Green Fluorescent Proteins / genetics
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Green Fluorescent Proteins / metabolism*
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HeLa Cells
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Humans
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Lamin Type A / genetics
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Lamin Type A / metabolism
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Microscopy, Confocal / methods
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Microscopy, Fluorescence / methods
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Mitosis / physiology
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Nuclear Envelope / chemistry
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Nuclear Envelope / metabolism*
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Sulfolobus / genetics
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Sulfolobus / physiology
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Transfection
Substances
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Archaeal Proteins
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Fluorescent Dyes
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Lamin Type A
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Green Fluorescent Proteins
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Biotin
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Fatty Acid Synthase, Type II
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Carbon-Nitrogen Ligases
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Acetyl-CoA Carboxylase
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biotin carboxyl carrier protein