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      A Molecular View of Kinetochore Assembly and Function

      review-article
      1 , 2 , * , 3 , 4 , *
      Biology
      MDPI
      centromere, kinetochore, cell division, mitosis, meiosis, KMN, CCAN, CENP-A

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          Abstract

          Kinetochores are large protein assemblies that connect chromosomes to microtubules of the mitotic and meiotic spindles in order to distribute the replicated genome from a mother cell to its daughters. Kinetochores also control feedback mechanisms responsible for the correction of incorrect microtubule attachments, and for the coordination of chromosome attachment with cell cycle progression. Finally, kinetochores contribute to their own preservation, across generations, at the specific chromosomal loci devoted to host them, the centromeres. They achieve this in most species by exploiting an epigenetic, DNA-sequence-independent mechanism; notable exceptions are budding yeasts where a specific sequence is associated with centromere function. In the last 15 years, extensive progress in the elucidation of the composition of the kinetochore and the identification of various physical and functional modules within its substructure has led to a much deeper molecular understanding of kinetochore organization and the origins of its functional output. Here, we provide a broad summary of this progress, focusing primarily on kinetochores of humans and budding yeast, while highlighting work from other models, and present important unresolved questions for future studies.

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          Most cited references386

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          The conserved KMN network constitutes the core microtubule-binding site of the kinetochore.

          The microtubule-binding interface of the kinetochore is of central importance in chromosome segregation. Although kinetochore components that stabilize, translocate on, and affect the polymerization state of microtubules have been identified, none have proven essential for kinetochore-microtubule interactions. Here, we examined the conserved KNL-1/Mis12 complex/Ndc80 complex (KMN) network, which is essential for kinetochore-microtubule interactions in vivo. We identified two distinct microtubule-binding activities within the KMN network: one associated with the Ndc80/Nuf2 subunits of the Ndc80 complex, and a second in KNL-1. Formation of the complete KMN network, which additionally requires the Mis12 complex and the Spc24/Spc25 subunits of the Ndc80 complex, synergistically enhances microtubule-binding activity. Phosphorylation by Aurora B, which corrects improper kinetochore-microtubule connections in vivo, reduces the affinity of the Ndc80 complex for microtubules in vitro. Based on these findings, we propose that the conserved KMN network constitutes the core microtubule-binding site of the kinetochore.
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            The Molecular Biology of Spindle Assembly Checkpoint Signaling Dynamics.

            The spindle assembly checkpoint is a safeguard mechanism that coordinates cell-cycle progression during mitosis with the state of chromosome attachment to the mitotic spindle. The checkpoint prevents mitotic cells from exiting mitosis in the presence of unattached or improperly attached chromosomes, thus avoiding whole-chromosome gains or losses and their detrimental effects on cell physiology. Here, I review a considerable body of recent progress in the elucidation of the molecular mechanisms underlying checkpoint signaling, and identify a number of unresolved questions.
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              Genome sequence, comparative analysis, and population genetics of the domestic horse.

              We report a high-quality draft sequence of the genome of the horse (Equus caballus). The genome is relatively repetitive but has little segmental duplication. Chromosomes appear to have undergone few historical rearrangements: 53% of equine chromosomes show conserved synteny to a single human chromosome. Equine chromosome 11 is shown to have an evolutionary new centromere devoid of centromeric satellite DNA, suggesting that centromeric function may arise before satellite repeat accumulation. Linkage disequilibrium, showing the influences of early domestication of large herds of female horses, is intermediate in length between dog and human, and there is long-range haplotype sharing among breeds.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Biology (Basel)
                Biology (Basel)
                biology
                Biology
                MDPI
                2079-7737
                24 January 2017
                March 2017
                : 6
                : 1
                : 5
                Affiliations
                [1 ]Department of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Otto-Hahn Straße 11, Dortmund 44227, Germany
                [2 ]Centre for Medical Biotechnology, Faculty of Biology, University Duisburg-Essen, Essen 45117, Germany
                [3 ]Ludwig Institute for Cancer Research, La Jolla, CA 92093, USA
                [4 ]Department of Cellular & Molecular Medicine, 9500 Gilman Dr., La Jolla, CA 92093, USA
                Author notes
                [* ]Correspondence: andrea.musacchio@ 123456mpi-dortmund.mpg.de (A.M.); abdesai@ 123456ucsd.edu (A.D.); Tel.: +49-231-133-2101 (A.M.); +1-858-534-9698 (A.D.); Fax: +49-231-133-2199 (A.M.)
                Article
                biology-06-00005
                10.3390/biology6010005
                5371998
                28125021
                757347be-82d3-4b13-955f-c6238f5e3fe2
                © 2017 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 13 December 2016
                : 17 January 2017
                Categories
                Review

                centromere,kinetochore,cell division,mitosis,meiosis,kmn,ccan,cenp-a
                centromere, kinetochore, cell division, mitosis, meiosis, kmn, ccan, cenp-a

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