File:Premitotic-Assembly-of-Human-CENPs--T-and--W-Switches-Centromeric-Chromatin-to-a-Mitotic-State-pbio.1001082.s010.ogv
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Premitotic-Assembly-of-Human-CENPs--T-and--W-Switches-Centromeric-Chromatin-to-a-Mitotic-State-pbio.1001082.s010.ogv (Ogg Theora video file, length 10 s, 508 × 508 pixels, 604 kbps, file size: 747 KB)
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[edit]DescriptionPremitotic-Assembly-of-Human-CENPs--T-and--W-Switches-Centromeric-Chromatin-to-a-Mitotic-State-pbio.1001082.s010.ogv |
English: Tubulin labeling confirms whole spindle motion in CENP-W depleted cells. HeLa-H2B-GFP cells were transfected with mCherry-tubulin to directly visualize spindle motion following transfection with pooled siRNAs against CENP-W. It is clear that the entire spindle is moving within cells that exhibit rolling. The spindle poles can be seen to split in some of these cells, as though the forces associated with spindle movement are able to disrupt spindle pole integrity. This may account for the multipolar spindles frequently observed in fixed specimens of CENP-W siRNA-treated cells. |
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Source | Video S4 from Prendergast L, van Vuuren C, Kaczmarczyk A, Doering V, Hellwig D, Quinn N, Hoischen C, Diekmann S, Sullivan K (2011). "Premitotic Assembly of Human CENPs -T and -W Switches Centromeric Chromatin to a Mitotic State". PLOS Biology. DOI:10.1371/journal.pbio.1001082. PMID 21695110. PMC: 3114758. | ||
Author | Prendergast L, van Vuuren C, Kaczmarczyk A, Doering V, Hellwig D, Quinn N, Hoischen C, Diekmann S, Sullivan K | ||
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Date/Time | Thumbnail | Dimensions | User | Comment | |
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current | 22:26, 14 November 2012 | 10 s, 508 × 508 (747 KB) | Open Access Media Importer Bot (talk | contribs) | Automatically uploaded media file from Open Access source. Please report problems or suggestions here. |
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Author | Prendergast L, van Vuuren C, Kaczmarczyk A, Doering V, Hellwig D, Quinn N, Hoischen C, Diekmann S, Sullivan K |
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Usage terms | http://creativecommons.org/licenses/by/3.0/ |
Image title | Tubulin labeling confirms whole spindle motion in CENP-W depleted cells. HeLa-H2B-GFP cells were transfected with mCherry-tubulin to directly visualize spindle motion following transfection with pooled siRNAs against CENP-W. It is clear that the entire spindle is moving within cells that exhibit rolling. The spindle poles can be seen to split in some of these cells, as though the forces associated with spindle movement are able to disrupt spindle pole integrity. This may account for the multipolar spindles frequently observed in fixed specimens of CENP-W siRNA-treated cells. |
Software used | Xiph.Org libtheora 1.1 20090822 (Thusnelda) |
Date and time of digitizing | 2011-06 |