Publication
Quantitative Microscopy Reveals Centromeric Chromatin Stability, Size, and Cell Cycle Mechanisms to Maintain Centromere Homeostasis
dc.contributor.author | Stankovic, Ana | |
dc.contributor.author | Jansen, Lars E. T. | |
dc.date.accessioned | 2017-11-23T12:05:45Z | |
dc.date.available | 2018-08-30T00:30:08Z | |
dc.date.issued | 2017-08-25 | |
dc.description | The deposited item is a book chapter and is part of the series "Centromeres and Kinetochores" published by the publisher Springer Verlag. The deposited book chapter is a post-print version and has been submitted to peer reviewing. There is no public supplementary material available for this publication. This publication hasn't any creative commons license associated. | pt_PT |
dc.description.abstract | Centromeres are chromatin domains specified by nucleosomes containing the histone H3 variant, CENP-A. This unique centromeric structure is at the heart of a strong self-templating epigenetic mechanism that renders centromeres heritable. We review how specific quantitative microscopy approaches have contributed to the determination of the copy number, architecture, size, and dynamics of centromeric chromatin and its associated centromere complex and kinetochore. These efforts revealed that the key to long-term centromere maintenance is the slow turnover of CENP-A nucleosomes, a critical size of the chromatin domain and its cell cycle-coupled replication. These features come together to maintain homeostasis of a chromatin locus that directs its own epigenetic inheritance and facilitates the assembly of the mitotic kinetochore. | pt_PT |
dc.description.sponsorship | There are no funders and sponsors indicated explicitly in the document. | pt_PT |
dc.description.version | info:eu-repo/semantics/publishedVersion | pt_PT |
dc.identifier.citation | Stankovic A., Jansen L.E.T. (2017) Quantitative Microscopy Reveals Centromeric Chromatin Stability, Size, and Cell Cycle Mechanisms to Maintain Centromere Homeostasis. In: Black B. (eds) Centromeres and Kinetochores. Progress in Molecular and Subcellular Biology, vol 56. Springer, Cham | pt_PT |
dc.identifier.doi | 10.1007/978-3-319-58592-5_6 | pt_PT |
dc.identifier.uri | http://hdl.handle.net/10400.7/812 | |
dc.language.iso | eng | pt_PT |
dc.peerreviewed | yes | pt_PT |
dc.publisher | Springer Verlag | pt_PT |
dc.relation | There are no funders and sponsors indicated explicitly in the document. | pt_PT |
dc.relation.publisherversion | https://link.springer.com/chapter/10.1007%2F978-3-319-58592-5_6 | pt_PT |
dc.subject | Microscopy | pt_PT |
dc.subject | Centromere | pt_PT |
dc.subject | Cell Cycle | pt_PT |
dc.subject | Nucleosomes | pt_PT |
dc.subject | Homeostasis | pt_PT |
dc.title | Quantitative Microscopy Reveals Centromeric Chromatin Stability, Size, and Cell Cycle Mechanisms to Maintain Centromere Homeostasis | pt_PT |
dc.type | book part | |
dspace.entity.type | Publication | |
oaire.citation.endPage | 162 | pt_PT |
oaire.citation.startPage | 139 | pt_PT |
oaire.citation.title | Progress in Molecular and Subcellular Biology | pt_PT |
oaire.citation.volume | 56 | pt_PT |
rcaap.embargofct | The deposited book chapter has 12 months of embargo period in terms of access, because of the book series's policies and the publisher's copyright policy, which require a period of embargo of 12 months. | pt_PT |
rcaap.rights | embargoedAccess | pt_PT |
rcaap.type | bookPart | pt_PT |
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