6 results match your criteria: "National Institute of Genetics and Graduate University for Advanced Studies (SOKENDAI)[Affiliation]"

Kinetochore assembly and function through the cell cycle.

Chromosoma

September 2016

Graduate School of Frontier Biosciences, Osaka University, Suita, Osaka, 565-0871, Japan.

Article Synopsis
  • The kinetochore is crucial for chromosome segregation in eukaryotes, acting as a link between spindle microtubules and chromosomes.
  • Recent research has shed light on how kinetochores are formed and function, as well as their role in centromere identity.
  • The review focuses on the interactions and regulatory mechanisms of key kinetochore components throughout the cell cycle.
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Article Synopsis
  • The kinetochore is crucial for attaching chromosomes to microtubules during mitosis, ensuring accurate chromosome segregation.
  • Key components of the kinetochore include histone-fold proteins CENP-S, -T, -W, and -X, which help establish kinetochore chromatin and form both heteromeric and heterotetrameric complexes.
  • This study focuses on the methods used to purify and characterize these kinetochore histone-fold complexes to better understand their formation and function.
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Dynamic changes in CCAN organization through CENP-C during cell-cycle progression.

Mol Biol Cell

November 2015

Graduate School of Frontier Biosciences, Osaka University, Suita, Osaka 565-0871, Japan Department of Molecular Genetics, National Institute of Genetics and Graduate University for Advanced Studies (SOKENDAI), Mishima, Shizuoka 411-8540, Japan

Article Synopsis
  • The kinetochore is vital for accurate chromosome separation during cell division, built on a protein network called CCAN at the chromosome's centromere.
  • While the CCAN consists of various subcomplexes, how these proteins organize to form a functional kinetochore throughout the cell cycle remains unclear.
  • Research shows that different regions of the CENP-C protein are responsible for its centromere localization in interphase and mitosis, suggesting that CCAN organization changes dynamically as the cell cycle progresses.
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Mammalian mitotic chromosome morphogenesis was analyzed by 4D live-cell and snapshot deconvolution fluorescence imaging. Prophase chromosomes, whose organization was previously unknown, are revealed to comprise co-oriented sister linear loop arrays displayed along a single, peripheral, regularly kinked topoisomerase II/cohesin/condensin II axis. Thereafter, rather than smooth, progressive compaction as generally envisioned, progression to metaphase is a discontinuous process involving chromosome expansion as well as compaction.

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Neocentromeres.

Curr Biol

October 2014

Wellcome Trust Centre for Cell Biology, University of Edinburgh, King's Buildings, Mayfield Road, Edinburgh, EH9 3JR, UK. Electronic address:

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The centromere: chromatin foundation for the kinetochore machinery.

Dev Cell

September 2014

Wellcome Trust Centre for Cell Biology, University of Edinburgh, King's Buildings, Mayfield Road, Edinburgh, EH9 3JR, UK. Electronic address:

Article Synopsis
  • Centromeres are chromatin structures marked by the histone H3 variant CENP-A, crucial for assembling kinetochores rather than defined by specific DNA sequences.
  • Recent studies, especially in vertebrates, reveal the importance of repetitive DNA sequences and various chromatin factors in the formation and activation of CENP-A chromatin for effective kinetochore assembly.
  • The review highlights classic and recent research on centromeric chromatin, including the use of artificial chromosomes to better understand centromere function.
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