Summary of ssbd-repos-00070

SSBD:database
URL

Name
ssbd-repos-00070 (70-Yoshida-KTMTDyn)
URL
DOI
-

Title
Timelapse confocal images and BDML files for quantitative information about the kinetochore microtubule dynamics during mouse oocytes meiosis
Description
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Submited Date
-
Release Date
2021-09-30
Updated Date
-
License
Funding information
-
File formats
Data size
371.5 GB

Organism
Mus musculus
Strain
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Cell Line
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Genes
BubR1, Hec1, Knl1
Proteins
ACA, Aurora A, Aurora B/C, CENP, CENP-C, H2B, INCENP, PP22A, PP2A, cyclin-B1, hINCENP

GO Molecular Function (MF)
NA
GO Biological Process (BP)
mitotic cell cycle
GO Cellular Component (CC)
chromosome, kinetochore microtubule
Study Type
Oocytes, Aurora Kinase C/metabolism, Oocytes/metabolism, Female, Protein-Serine-Threonine Kinases/metabolism, Oocytes/cytology, Meiosis/physiology, CDC2 Protein Kinase/metabolism, CDC2 Protein Kinase, Mice, Computer-Assisted, Chromosome Segregation, Kinetochores, Image Processing, Protein Phosphatase 2/metabolism, Protein-Serine-Threonine Kinases, Phosphorylation, Animals, Microtubules, Aurora Kinase B, Cell Cycle Proteins/metabolism, Aurora Kinase B/metabolism, Fluorescent Antibody Technique, Aurora Kinase C, Cell Cycle Proteins, Kinetochores/physiology, Protein Phosphatase 2, Microtubules/physiology, Meiosis
Imaging Methods
time lapse microscopy, fluorescence microscopy

Method Summary
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Related paper(s)

Shuhei Yoshida, Masako Kaido, Tomoya S Kitajima (2015) Inherent Instability of Correct Kinetochore-Microtubule Attachments during Meiosis I in Oocytes., Developmental cell, Volume 33, Number 5, pp. 589-602

Published in 2015 Jun 8 (Electronic publication in May 28, 2015, midnight )

(Abstract) A model for mitosis suggests that correct kinetochore-microtubule (KT-MT) attachments are stabilized by spatial separation of the attachment sites from Aurora B kinase through sister KT stretching. However, the spatiotemporal regulation of attachment stability during meiosis I (MI) in oocytes remains unclear. Here, we found that in mouse oocytes, Aurora B and C (B/C) are located in close proximity to KT-MT attachment sites after bivalent stretching due to an intrinsic property of the MI chromosomes. The Aurora B/C activity destabilizes correct attachments while allowing a considerable amount of incorrect attachments to form. KT-MT attachments are eventually stabilized through KT dephosphorylation by PP2A-B56 phosphatase, which is progressively recruited to KTs depending on the BubR1 phosphorylation resulting from the timer Cdk1 and independent of bivalent stretching. Thus, oocytes lack a mechanism for coordinating bivalent stretching and KT phosphoregulation during MI, which may explain the high frequency of KT-MT attachment errors.
(MeSH Terms)

Contact(s)
Tomoya S. Kitajima
Organization(s)
RIKEN , Center for Biosystems Dynamics Research , Laboratory for Chromosome Segregation
Image Data Contributors
Quantitative Data Contributors

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