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      Regulation of spindle integrity and mitotic fidelity by BCCIP

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          Abstract

          Centrosomes together with the mitotic spindle ensure the faithful distribution of chromosomes between daughter cells, and spindle orientation is a major determinant of cell fate during tissue regeneration. Spindle defects are not only an impetus of chromosome instability but are also a cause of developmental disorders involving defective asymmetric cell division. In this work, we demonstrate BCCIP, especially BCCIPα, as a previously unidentified component of the mitotic spindle pole and the centrosome. We demonstrate that BCCIP localizes proximal to the mother centriole and participates in microtubule organization and then redistributes to the spindle pole to ensure faithful spindle architecture. We find that BCCIP depletion leads to morphological defects, disoriented mitotic spindles, chromosome congression defects and delayed mitotic progression. Our study identifies BCCIP as a novel factor critical for microtubule regulation and explicates a mechanism utilized by BCCIP in tumor suppression.

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          Most cited references58

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          Gene splicing and mutagenesis by PCR-driven overlap extension.

          Extension of overlapping gene segments by PCR is a simple, versatile technique for site-directed mutagenesis and gene splicing. Initial PCRs generate overlapping gene segments that are then used as template DNA for another PCR to create a full-length product. Internal primers generate overlapping, complementary 3' ends on the intermediate segments and introduce nucleotide substitutions, insertions or deletions for site-directed mutagenesis, or for gene splicing, encode the nucleotides found at the junction of adjoining gene segments. Overlapping strands of these intermediate products hybridize at this 3' region in a subsequent PCR and are extended to generate the full-length product amplified by flanking primers that can include restriction enzyme sites for inserting the product into an expression vector for cloning purposes. The highly efficient generation of mutant or chimeric genes by this method can easily be accomplished with standard laboratory reagents in approximately 1 week.
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            Dissecting self-renewal in stem cells with RNA interference.

            We present an integrated approach to identify genetic mechanisms that control self-renewal in mouse embryonic stem cells. We use short hairpin RNA (shRNA) loss-of-function techniques to downregulate a set of gene products whose expression patterns suggest self-renewal regulatory functions. We focus on transcriptional regulators and identify seven genes for which shRNA-mediated depletion negatively affects self-renewal, including four genes with previously unrecognized roles in self-renewal. Perturbations of these gene products are combined with dynamic, global analyses of gene expression. Our studies suggest specific biological roles for these molecules and reveal the complexity of cell fate regulation in embryonic stem cells.
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              Self-organization of microtubules into bipolar spindles around artificial chromosomes in Xenopus egg extracts.

              Functional nuclei and mitotic spindles are shown to assemble around DNA-coated beads incubated in Xenopus egg extracts. Bipolar spindles assemble in the absence of centrosomes and kinetochores, indicating that bipolarity is an intrinsic property of microtubules assembling around chromatin in a mitotic cytoplasm. Microtubules nucleated at dispersed sites with random polarity rearrange into two arrays of uniform polarity. Spindle-pole formation requires cytoplasmic dynein-dependent translocation of microtubules across one another. It is proposed that spindles form in the absence of centrosomes by motor-dependent sorting of microtubules according to their polarity.
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                Author and article information

                Journal
                Oncogene
                Oncogene
                Oncogene
                Nature Publishing Group
                0950-9232
                1476-5594
                17 August 2017
                10 April 2017
                : 36
                : 33
                : 4750-4766
                Affiliations
                [1 ]Rutgers Cancer Institute of New Jersey , 195 Little Albany Street, New Brunswick, New Jersey 08903, USA
                [2 ]Department of Radiation Oncology, Rutgers Robert Wood Johnson Medical School , New Brunswick, New Jersey, USA
                [3 ]Department of Medicine, Rutgers Robert Wood Johnson Medical School , New Brunswick, New Jersey, USA
                [4 ]Department of Molecular Biology and Biochemistry, Rutgers, The State University of New Jersey , Piscataway, New Jersey, USA
                Author notes
                [* ]Department of Radiation Oncology, Rutgers Cancer Institute of New Jersey/Rutgers University , 195 Little Albany Street, New Brunswick, New Jersey, 08903, USA. E-mail: shenzh@ 123456cinj.rutgers.edu
                [5]

                Current address: The First Hospital of Jilin University, Changchun, Jilin Province, China.

                Author information
                http://orcid.org/0000-0003-2834-0309
                Article
                onc201792
                10.1038/onc.2017.92
                5561484
                28394342
                31298eb4-be07-4fea-9cca-9d59863d28cb
                Copyright © 2017 The Author(s)

                This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/

                History
                : 15 September 2016
                : 11 January 2017
                : 26 February 2017
                Categories
                Original Article

                Oncology & Radiotherapy
                Oncology & Radiotherapy

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