New mitotic regulators released from chromatin

Faithful action of the mitotic spindle segregates duplicated chromosomes into daughter cells. Perturbations of this process result in chromosome mis-segregation, leading to chromosomal instability and cancer development. Chromosomes are not simply passengers segregated by spindle microtubules but ra...

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Bibliographic Details
Main Authors: Yokoyama, Hideki (Author) , Gruss, Oliver (Author)
Format: Article (Journal)
Language:English
Published: 16 December 2013
In: Frontiers in oncology
Year: 2013, Volume: 3, Pages: 1-6
ISSN:2234-943X
DOI:10.3389/fonc.2013.00308
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.3389/fonc.2013.00308
Verlag, lizenzpflichtig, Volltext: https://www.frontiersin.org/articles/10.3389/fonc.2013.00308/full
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Author Notes:Hideki Yokoyama and Oliver J. Gruss
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Summary:Faithful action of the mitotic spindle segregates duplicated chromosomes into daughter cells. Perturbations of this process result in chromosome mis-segregation, leading to chromosomal instability and cancer development. Chromosomes are not simply passengers segregated by spindle microtubules but rather play a major active role in spindle assembly. The GTP bound form of the Ran GTPase (RanGTP), produced around chromosomes, locally activates spindle assembly factors. Recent studies have uncovered that chromosomes organize mitosis beyond spindle formation. They distinctly regulate other mitotic events, such as spindle maintenance in anaphase, which is essential for chromosome segregation. Furthermore, the direct function of chromosomes is not only to produce RanGTP but, in addition, to release key mitotic regulators from chromatin. Chromatin-remodeling factors and nuclear pore complex proteins, which have established functions on chromatin in interphase, dissociate from mitotic chromatin and function in spindle assembly or maintenance. Thus, chromosomes actively organize their own segregation using chromatin-releasing mitotic regulators as well as RanGTP.
Item Description:Gesehen am 26.07.2021
Physical Description:Online Resource
ISSN:2234-943X
DOI:10.3389/fonc.2013.00308