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Cytoophidium assembly reflects upregulation of IMPDH activity

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...

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Autores principales: Chang, Chia-Chun, Lin, Wei-Cheng, Pai, Li-Mei, Lee, Hsuan-Shu, Wu, Shinn-Chih, Ding, Shih-Torng, Liu, Ji-Long, Sung, Li-Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4610212/
https://www.ncbi.nlm.nih.gov/pubmed/26303200
http://dx.doi.org/10.1242/jcs.175265
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author Chang, Chia-Chun
Lin, Wei-Cheng
Pai, Li-Mei
Lee, Hsuan-Shu
Wu, Shinn-Chih
Ding, Shih-Torng
Liu, Ji-Long
Sung, Li-Ying
author_facet Chang, Chia-Chun
Lin, Wei-Cheng
Pai, Li-Mei
Lee, Hsuan-Shu
Wu, Shinn-Chih
Ding, Shih-Torng
Liu, Ji-Long
Sung, Li-Ying
author_sort Chang, Chia-Chun
collection PubMed
description 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.
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spelling pubmed-46102122015-11-04 Cytoophidium assembly reflects upregulation of IMPDH activity Chang, Chia-Chun Lin, Wei-Cheng Pai, Li-Mei Lee, Hsuan-Shu Wu, Shinn-Chih Ding, Shih-Torng Liu, Ji-Long Sung, Li-Ying J Cell Sci Short Report 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. The Company of Biologists 2015-10-01 /pmc/articles/PMC4610212/ /pubmed/26303200 http://dx.doi.org/10.1242/jcs.175265 Text en © 2015. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Short Report
Chang, Chia-Chun
Lin, Wei-Cheng
Pai, Li-Mei
Lee, Hsuan-Shu
Wu, Shinn-Chih
Ding, Shih-Torng
Liu, Ji-Long
Sung, Li-Ying
Cytoophidium assembly reflects upregulation of IMPDH activity
title Cytoophidium assembly reflects upregulation of IMPDH activity
title_full Cytoophidium assembly reflects upregulation of IMPDH activity
title_fullStr Cytoophidium assembly reflects upregulation of IMPDH activity
title_full_unstemmed Cytoophidium assembly reflects upregulation of IMPDH activity
title_short Cytoophidium assembly reflects upregulation of IMPDH activity
title_sort cytoophidium assembly reflects upregulation of impdh activity
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4610212/
https://www.ncbi.nlm.nih.gov/pubmed/26303200
http://dx.doi.org/10.1242/jcs.175265
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