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  RuvB-like ATPases function in chromatin decondensation at the end of mitosis

Magalska, A., Schellhaus, A., Moreno Andrés, D., Zanini, F., Schooley, A., Sachdev, R., et al. (2014). RuvB-like ATPases function in chromatin decondensation at the end of mitosis. Developmental Cell, 31(3), 305-318. doi:10.1016/j.devcel.2014.09.001.

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Magalska, A, Autor           
Schellhaus, AK, Autor           
Moreno Andrés, D, Autor           
Zanini, F1, Autor           
Schooley, A, Autor           
Sachdev, R, Autor           
Schwarz, H2, Autor           
Madlung, J, Autor
Antonin, W, Autor           
Affiliations:
1Research Group Evolutionary Dynamics and Biophysics, Max Planck Institute for Developmental Biology, Max Planck Society, ou_3377926              
2Electron Microscopy, Max Planck Institute for Developmental Biology, Max Planck Society, Max-Planck-Ring 5, 72076 Tübingen, DE, ou_3375794              

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 Zusammenfassung: Chromatin undergoes extensive structural changes during the cell cycle. Upon mitotic entry, metazoan chromatin undergoes tremendous condensation, creating mitotic chromosomes with 50-fold greater compaction relative to interphase chromosomes. At the end of mitosis, chromosomes reestablish functional interphase chromatin competent for replication and transcription through a decondensation process that is cytologically well described. However, the underlying molecular events and factors remain unidentified. We describe a cell-free system that recapitulates chromatin decondensation based on purified mitotic chromatin and Xenopus egg extracts. Using biochemical fractionation, we identify RuvB-like ATPases as chromatin decondensation factors and demonstrate that their ATPase activity is essential for decondensation. Our results show that decompaction of metaphase chromosomes is not merely an inactivation of known chromatin condensation factors but rather an active process requiring specific molecular machinery. Our cell-free system provides an important tool for further molecular characterization of chromatin decondensation and its coordination with concomitant processes.

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 Datum: 2014-11
 Publikationsstatus: Erschienen
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 Identifikatoren: DOI: 10.1016/j.devcel.2014.09.001
PMID: 25443297
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Titel: Developmental Cell
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Cambridge, Mass. : Cell Press
Seiten: - Band / Heft: 31 (3) Artikelnummer: - Start- / Endseite: 305 - 318 Identifikator: ISSN: 1534-5807
CoNE: https://pure.mpg.de/cone/journals/resource/111006902714134