Summary of ssbd-repos-000138

SSBD:database
URL

Name
ssbd-repos-000138 (138-Ito-SPBDyn)
URL
DOI
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Title
Time-lapse images of nucleolus and spindle pole body (SPB) movements in the sid4-mCherry and Cut11-GFP expressing S. pombe cells cultured in different medium
Description
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Submited Date
-
Release Date
2022-03-31
Updated Date
-
License
Funding information
-
File formats
Data size
62.8 GB

Organism
Schizosaccharomyces pombe
Strain
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Cell Line
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Genes
Cut11, sid4
Proteins
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GO Molecular Function (MF)
NA
GO Biological Process (BP)
oscillatory muscle contraction
GO Cellular Component (CC)
spindle pole body, nuclear membrane
Study Type
Centromere/metabolism, Centromere, Glucose/metabolism, Ammonium Chloride/metabolism, Schizosaccharomyces/cytology, Adenosine Triphosphate, Schizosaccharomyces/metabolism, Ammonium Chloride, Glucose, Schizosaccharomyces, Adenosine Triphosphate/metabolism, Spindle Pole Bodies, Spindle Pole Bodies/metabolism
Imaging Methods
time lapse microscopy

Method Summary
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Related paper(s)

Hiroaki Ito, Takeshi Sugawara, Soya Shinkai, Satoshi Mizukawa, Ayaka Kondo, Hisamichi Senda, Kengo Sawai, Koki Ito, Sayaka Suzuki, Masakatsu Takaine, Satoshi Yoshida, Hiromi Imamura, Kenji Kitamura, Toshinori Namba, Shin-Ichi Tate, Masaru Ueno (2019) Spindle pole body movement is affected by glucose and ammonium chloride in fission yeast., Biochemical and biophysical research communications, Volume 511, Number 4, pp. 820-825

Published in 2019 Apr 16 (Electronic publication in March 4, 2019, midnight )

(Abstract) The complexity of chromatin dynamics is orchestrated by several active processes. In fission yeast, the centromeres are clustered around the spindle pole body (SPB) and oscillate in a microtubule- and adenosine triphosphate (ATP)-dependent manner. However, whether and how SPB oscillation are affected by different environmental conditions remain poorly understood. In this study, we quantitated movements of the SPB component, which colocalizes with the centromere in fission yeast. We found that SPB movement was significantly reduced at low glucose concentrations. Movement of the SPB was also affected by the presence of ammonium chloride. Power spectral analysis revealed that periodic movement of the SPB is disrupted by low glucose concentrations. Measurement of ATP levels in living cells by quantitative single-cell imaging suggests that ATP levels are not the only determinant of SPB movement. Our results provide novel insight into how SPB movement is regulated by cellular energy status and additional factors such as the medium nutritional composition.
(MeSH Terms)

Contact(s)
Masaru Ueno
Organization(s)
Graduate School of Advanced Sciences of Matter, Hiroshima University , Department of Molecular Biotechnology , Ueno Laboratory
Image Data Contributors
Quantitative Data Contributors

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