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    Crosstalk between NDR kinase pathways coordinates cell cycle dependent actin rearrangements

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    Authors
    Gupta, Sneha
    McCollum, Dannel
    UMass Chan Affiliations
    Program in Cell Dynamics
    Department of Microbiology and Physiological Systems
    Document Type
    Journal Article
    Publication Date
    2011-11-11
    Keywords
    Cell Cycle Checkpoints
    Cytokinesis
    Actin Cytoskeleton
    Protein-Serine-Threonine Kinases
    Cell Polarity
    Cell Biology
    Cellular and Molecular Physiology
    
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    Link to Full Text
    http://dx.doi.org/10.1186/1747-1028-6-19
    Abstract
    Regulation of cytoskeletal remodeling is essential for cell cycle transitions. In fission yeast two NDR kinase signaling cascades, MOR and SIN, regulate the actin cytoskeleton to promote polarized growth during interphase and cytokinesis respectively. Our understanding of how these signaling pathways are coordinated to assist transition between the two cell-cycle stages is limited. Here, we review work from our laboratory, which reveals that cross talk between the SIN and MOR pathways is required for inhibition of interphase polarity programs during cytokinesis. Given the conservation of NDR kinase signaling pathways, our results may define general mechanisms by which these pathways are coordinated in higher organisms.
    Source
    Cell Div. 2011 Nov 11;6:19. Link to article on publisher's site
    DOI
    10.1186/1747-1028-6-19
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/39457
    PubMed ID
    22079013; 22079013
    Notes

    First author Sneha Gupta is a doctoral student in the Interdisciplinary Graduate Program in the Graduate School of Biomedical Sciences (GSBS) at UMass Medical School.

    Related Resources
    Link to Article in PubMed
    Rights
    © 2011 Gupta and McCollum; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
    ae974a485f413a2113503eed53cd6c53
    10.1186/1747-1028-6-19
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