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      Neuronal cell cycle: the neuron itself and its circumstances

      review-article
      1 , 1 , 2
      Cell Cycle
      Taylor & Francis
      apoptosis, cell cycle re-entry, mitosis, neuron, S-phase, tetraploid, AD, Alzheimer disease, BDNF, brain-derived neurotrophic factor, BrdU, 5-bromo-2′-deoxyuridine, Cdk, cyclin-dependent kinase, CKI, Cdk-inhibitor, Cip/Kip, cyclin inhibitor protein/kinase inhibitor protein, CNS, central nervous system, G0, quiescent state, G1, growth phase 1, G2, growth phase 2, Ink, inhibitor of kinase, Mcm2, minichromosome maintenance 2, p38MAPK, p38 mitogen-activated protein kinase, p75NTR, neurotrophin receptor p75, PCNA, proliferating cell nuclear antigen, PD, Parkinson disease, Rb, Retinoblastoma, RGCs, retinal ganglion cells, S-phase, synthesis phase.

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          Abstract

          Neurons are usually regarded as postmitotic cells that undergo apoptosis in response to cell cycle reactivation. Nevertheless, recent evidence indicates the existence of a defined developmental program that induces DNA replication in specific populations of neurons, which remain in a tetraploid state for the rest of their adult life. Similarly, de novo neuronal tetraploidization has also been described in the adult brain as an early hallmark of neurodegeneration. The aim of this review is to integrate these recent developments in the context of cell cycle regulation and apoptotic cell death in neurons. We conclude that a variety of mechanisms exists in neuronal cells for G1/S and G2/M checkpoint regulation. These mechanisms, which are connected with the apoptotic machinery, can be modulated by environmental signals and the neuronal phenotype itself, thus resulting in a variety of outcomes ranging from cell death at the G1/S checkpoint to full proliferation of differentiated neurons.

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          Most cited references117

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          CDK inhibitors: positive and negative regulators of G1-phase progression.

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            CDK inhibitors: cell cycle regulators and beyond.

            First identified as cell cycle inhibitors mediating the growth inhibitory cues of upstream signaling pathways, the cyclin-CDK inhibitors of the Cip/Kip family p21Cip1, p27Kip1, and p57Kip2 have emerged as multifaceted proteins with functions beyond cell cycle regulation. In addition to regulating the cell cycle, Cip/Kip proteins play important roles in apoptosis, transcriptional regulation, cell fate determination, cell migration and cytoskeletal dynamics. A complex phosphorylation network modulates Cip/Kip protein functions by altering their subcellular localization, protein-protein interactions, and stability. These functions are essential for the maintenance of normal cell and tissue homeostasis, in processes ranging from embryonic development to tumor suppression.
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              Cell cycle control across the eukaryotic kingdom.

              Almost two billion years of evolution have generated a vast and amazing variety of eukaryotic life with approximately 8.7 million extant species. Growth and reproduction of all of these organisms depend on faithful duplication and distribution of their chromosomes to the newly forming daughter cells in a process called the cell cycle. However, most of what is known today about cell cycle control comes from a few model species that belong to the unikonts; that is, to only one of five 'supergroups' that comprise the eukaryotic kingdom. Recently, analyzing species from distantly related clades is providing insights into general principles of cell cycle regulation and shedding light on its evolution. Here, referring to animal and fungal as opposed to non-unikont systems, especially flowering plants from the archaeplastid supergroup, we compare the conservation of central cell cycle regulator functions, the structure of network topologies, and the evolutionary dynamics of substrates of core cell cycle kinases. Copyright © 2013 Elsevier Ltd. All rights reserved.
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                Author and article information

                Journal
                Cell Cycle
                Cell Cycle
                KCCY
                Cell Cycle
                Taylor & Francis
                1538-4101
                1551-4005
                15 January 2015
                March 2015
                : 14
                : 5
                : 712-720
                Affiliations
                [1 ]Department of Molecular, Cellular and Developmental Neurobiology; Instituto Cajal; Consejo Superior de Investigaciones Científicas (IC-CSIC) ; Madrid, Spain
                []Current address: Department of Cell Biology; University of Valencia ; Burjassot, Spain
                Author notes
                [* ]Correspondence to: José M Frade; Email: frade@ 123456cajal.csic.es
                Article
                1004937
                10.1080/15384101.2015.1004937
                4418291
                25590687
                5169679f-4b90-47cc-bbdb-2938100e0b6d
                © 2015 The Author(s). Published with license by Taylor & Francis Group, LLC© José M Frade and María C Ovejero-Benito

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License http://creativecommons.org/licenses/by-nc/3.0/, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.

                History
                : 19 November 2014
                : 23 December 2014
                : 28 December 2014
                Page count
                Figures: 2, Tables: 1, References: 132, Pages: 9
                Categories
                Review

                Cell biology
                apoptosis,cell cycle re-entry,mitosis,neuron,s-phase,tetraploid,ad, alzheimer disease,bdnf, brain-derived neurotrophic factor,brdu, 5-bromo-2′-deoxyuridine,cdk, cyclin-dependent kinase,cki, cdk-inhibitor,cip/kip, cyclin inhibitor protein/kinase inhibitor protein,cns, central nervous system,g0, quiescent state,g1, growth phase 1,g2, growth phase 2,ink, inhibitor of kinase,mcm2, minichromosome maintenance 2,p38mapk, p38 mitogen-activated protein kinase,p75ntr, neurotrophin receptor p75,pcna, proliferating cell nuclear antigen,pd, parkinson disease,rb, retinoblastoma,rgcs, retinal ganglion cells,s-phase, synthesis phase.

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