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      Diversity is the spice of life: An overview of how cytokinesis regulation varies with cell type

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          Abstract

          Cytokinesis is required to physically cleave a cell into two daughters at the end of mitosis. Decades of research have led to a comprehensive understanding of the core cytokinesis machinery and how it is regulated in animal cells, however this knowledge was generated using single cells cultured in vitro, or in early embryos before tissues develop. This raises the question of how cytokinesis is regulated in diverse animal cell types and developmental contexts. Recent studies of distinct cell types in the same organism or in similar cell types from different organisms have revealed striking differences in how cytokinesis is regulated, which includes different threshold requirements for the structural components and the mechanisms that regulate them. In this review, we highlight these differences with an emphasis on pathways that are independent of the mitotic spindle, and operate through signals associated with the cortex, kinetochores, or chromatin.

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          Most cited references128

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          Classical nuclear localization signals: definition, function, and interaction with importin alpha.

          The best understood system for the transport of macromolecules between the cytoplasm and the nucleus is the classical nuclear import pathway. In this pathway, a protein containing a classical basic nuclear localization signal (NLS) is imported by a heterodimeric import receptor consisting of the beta-karyopherin importin beta, which mediates interactions with the nuclear pore complex, and the adaptor protein importin alpha, which directly binds the classical NLS. Here we review recent studies that have advanced our understanding of this pathway and also take a bioinformatics approach to analyze the likely prevalence of this system in vivo. Finally, we describe how a predicted NLS within a protein of interest can be confirmed experimentally to be functionally important.
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            Aurora B-mediated abscission checkpoint protects against tetraploidization.

            Genomic abnormalities are often seen in tumor cells, and tetraploidization, which results from failures during cytokinesis, is presumed to be an early step in cancer formation. Here, we report a cell division control mechanism that prevents tetraploidization in human cells with perturbed chromosome segregation. First, we found that Aurora B inactivation promotes completion of cytokinesis by abscission. Chromosome bridges sustained Aurora B activity to posttelophase stages and thereby delayed abscission at stabilized intercellular canals. This was essential to suppress tetraploidization by furrow regression in a pathway further involving the phosphorylation of mitotic kinesin-like protein 1 (Mklp1). We propose that Aurora B is part of a sensor that responds to unsegregated chromatin at the cleavage site. Our study provides evidence that in human cells abscission is coordinated with the completion of chromosome segregation to protect against tetraploidization by furrow regression.
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              Cytokinesis in animal cells.

              Cytokinesis, the final step in cell division, partitions the contents of a single cell into two. In animal cells, cytokinesis occurs through cortical remodeling orchestrated by the anaphase spindle. Cytokinesis relies on a tight interplay between signaling and cellular mechanics and has attracted the attention of both biologists and physicists for more than a century. In this review, we provide an overview of four topics in animal cell cytokinesis: (a) signaling between the anaphase spindle and cortex, (b) the mechanics of cortical remodeling, (c) abscission, and (d) regulation of cytokinesis by the cell cycle machinery. We report on recent progress in these areas and highlight some of the outstanding questions that these findings bring into focus.
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                Author and article information

                Contributors
                Journal
                Front Cell Dev Biol
                Front Cell Dev Biol
                Front. Cell Dev. Biol.
                Frontiers in Cell and Developmental Biology
                Frontiers Media S.A.
                2296-634X
                07 November 2022
                2022
                : 10
                : 1007614
                Affiliations
                [1] 1 Department of Biology , McGill University , Montreal, QC, Canada
                [2] 2 Department of Biology , Concordia University , Montreal, QC, Canada
                Author notes

                Edited by: Paola Vagnarelli, Brunel University London, United Kingdom

                Reviewed by: Gang Zhang, Qingdao University, China

                Ana Xavier De Carvalho, Universidade do Porto, Portugal

                *Correspondence: Alisa Piekny, alisa.piekny@ 123456concordia.ca

                This article was submitted to Cell Growth and Division, a section of the journal Frontiers in Cell and Developmental Biology

                Article
                1007614
                10.3389/fcell.2022.1007614
                9676254
                36420142
                81889e8b-fc45-44c6-9df5-98f23b6f648b
                Copyright © 2022 Ozugergin and Piekny.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 30 July 2022
                : 24 October 2022
                Funding
                Funded by: Natural Sciences and Engineering Research Council of Canada , doi 10.13039/501100000038;
                Award ID: 04161-2017
                Categories
                Cell and Developmental Biology
                Mini Review

                mitosis,cytokinesis,rhoa,actomyosin,mitotic spindle,chromatin
                mitosis, cytokinesis, rhoa, actomyosin, mitotic spindle, chromatin

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