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Directional motion of foreign plasmid DNA to nuclear HP1 foci
Ondrej V., Kozubek S., Lukásová E., Falk M., Matula P., Matula P., Kozubek M.
Language English Country Netherlands
NLK
ProQuest Central
from 1997-02-01 to 1 year ago
Health & Medicine (ProQuest)
from 1997-02-01 to 1 year ago
- MeSH
- Biological Transport physiology genetics MeSH
- Cell Nucleus physiology MeSH
- Chromosomal Proteins, Non-Histone physiology genetics MeSH
- DNA physiology genetics MeSH
- Financing, Organized MeSH
- Heterochromatin MeSH
- Humans MeSH
- Microscopy MeSH
- Cell Line, Tumor MeSH
- Plasmids physiology genetics MeSH
- Transfection MeSH
- Check Tag
- Humans MeSH
Movement of labelled plasmid DNA relative to heterochromatin foci in nuclei, visualized with HP1-GFP, was studied using live-cell imaging and object tracking. In addition to Brownian motion of plasmid DNA we found a pronounced, non-random movement of plasmid DNA towards the nearest HP1 focus, while time-lapse microscopy showed that HP1 foci are relatively immobile and positionally stable. The movement of plasmid DNA was much faster than that of the HP1 foci. Contact of transgene DNA with an HP1 focus usually resulted in cessation of the directional motion. Moreover, the motion of plasmid DNA inside the heterochromatin compartment was more restricted (limited to 0.25 microm) than when the plasmid DNA was outside heterochromatin (R = 0.7 microm). Three days after transfection most of the foreign labelled DNA colocalized with centromeric heterochromatin.
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- $a Directional motion of foreign plasmid DNA to nuclear HP1 foci / $c Ondrej V., Kozubek S., Lukásová E., Falk M., Matula P., Matula P., Kozubek M.
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- $a Laboratory of Molecular Cytology and Cytometry, Institute of Biophysics AS CR, Kralovopolska 135, Brno, 612 65, Czech Republic. ondrej@ibp.cz
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- $a Movement of labelled plasmid DNA relative to heterochromatin foci in nuclei, visualized with HP1-GFP, was studied using live-cell imaging and object tracking. In addition to Brownian motion of plasmid DNA we found a pronounced, non-random movement of plasmid DNA towards the nearest HP1 focus, while time-lapse microscopy showed that HP1 foci are relatively immobile and positionally stable. The movement of plasmid DNA was much faster than that of the HP1 foci. Contact of transgene DNA with an HP1 focus usually resulted in cessation of the directional motion. Moreover, the motion of plasmid DNA inside the heterochromatin compartment was more restricted (limited to 0.25 microm) than when the plasmid DNA was outside heterochromatin (R = 0.7 microm). Three days after transfection most of the foreign labelled DNA colocalized with centromeric heterochromatin.
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