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  4. Cytoophidium assembly reflects upregulation of IMPDH activity.
 
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Cytoophidium assembly reflects upregulation of IMPDH activity.

Journal
Journal of cell science
Journal Volume
128
Journal Issue
19
Start Page
3550
End Page
3555
ISSN
1477-9137
Date Issued
2015-10-01
Author(s)
Chang, Chia-Chun  
Lin, Wei-Cheng
Pai, Li-Mei
Lee, Hsuan-Shu  
Wu, Shinn-Chih  
Ding, Shih-Torng  
Liu, Ji-Long
Sung, Li-Ying  
DOI
10.1242/jcs.175265
URI
https://www.scopus.com/pages/publications/84946100005
https://scholars.lib.ntu.edu.tw/handle/123456789/731153
Abstract
Cytidine triphosphate synthase (CTPS) and inosine monophosphate dehydrogenase (IMPDH) (both of which have two isoforms) can form fiber-like subcellular structures termed 'cytoophidia' under certain circumstances in mammalian cells. Although it has been shown that filamentation of CTPS downregulates its activity by disturbing conformational changes, the activity of IMPDH within cytoophidia is still unclear. Most previous IMPDH cytoophidium studies were performed under conditions involving inhibitors that impair GTP synthesis. Here, we show that IMPDH forms cytoophidia without inhibition of GTP synthesis. First, we find that an elevated intracellular CTP concentration or treatment with 3'-deazauridine, a CTPS inhibitor, promotes IMPDH cytoophidium formation and increases the intracellular GTP pool size. Moreover, restriction of cell growth triggers the disassembly of IMPDH cytoophidia, implying that their presence is correlated with active cell metabolism. Finally, we show that the presence of IMPDH cytoophidia in mouse pancreatic islet cells might correlate with nutrient uptake in the animal. Collectively, our findings reveal that formation of IMPDH cytoophidia reflects upregulation of purine nucleotide synthesis, suggesting that the IMPDH cytoophidium plays a role distinct from that of the CTPS cytoophidium in controlling intracellular nucleotide homeostasis.
Subjects
CTPS
Cytoophidium
IMPDH
Nucleotide
SDGs

[SDGs]SDG3

Publisher
Company of Biologists
Type
journal article

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