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Visualizing telomere dynamics in living mammalian cells using PNA probes
被引:157
作者:
Molenaar, C
Wiesmeijer, K
Verwoerd, NP
Khazen, S
Eils, R
Tanke, HJ
Dirks, RW
[1
]
机构:
[1] Leiden Univ, Med Ctr, Dept Mol Cell Biol, NL-2333 AL Leiden, Netherlands
[2] Deutsch Krebsforschungszentrum, Intelligent Bioinformat Syst, D-69120 Heidelberg, Germany
关键词:
ALT;
live cell imaging;
PML;
PNA;
telomeres;
D O I:
10.1093/emboj/cdg633
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Chromosome ends are protected from degradation by the presence of the highly repetitive hexanucleotide sequence of TTAGGG and associated proteins. These so-called telomeric complexes are suggested to play an important role in establishing a functional nuclear chromatin organization. Using peptide nucleic acid (PNA) probes, we studied the dynamic behavior of telomeric DNA repeats in living human osteosarcoma U2OS cells. A fluorescent cy3-labeled PNA probe was introduced in living cells by glass bead loading and was shown to specifically associate with telomeric DNA shortly afterwards. Telomere dynamics were imaged for several hours using digital fluorescence microscopy. While the majority of telomeres revealed constrained diffusive movement, individual telomeres in a human cell nucleus showed significant directional movements. Also, a subfraction of telomeres were shown to associate and dissociate, suggesting that in vivo telomere clusters are not stable but dynamic structures. Furthermore, telomeres were shown to associate with promyelocytic leukemia (PML) bodies in a dynamic manner.
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页码:6631 / 6641
页数:11
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