Cargando…

Only One Isoform of Drosophila melanogaster CTP Synthase Forms the Cytoophidium

CTP synthase is an essential enzyme that plays a key role in energy metabolism. Several independent studies have demonstrated that CTP synthase can form an evolutionarily conserved subcellular structure termed cytoophidium. In budding yeast, there are two isoforms of CTP synthase and both isoforms l...

Descripción completa

Detalles Bibliográficos
Autores principales: Azzam, Ghows, Liu, Ji-Long
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3573105/
https://www.ncbi.nlm.nih.gov/pubmed/23459760
http://dx.doi.org/10.1371/journal.pgen.1003256
_version_ 1782259405232799744
author Azzam, Ghows
Liu, Ji-Long
author_facet Azzam, Ghows
Liu, Ji-Long
author_sort Azzam, Ghows
collection PubMed
description CTP synthase is an essential enzyme that plays a key role in energy metabolism. Several independent studies have demonstrated that CTP synthase can form an evolutionarily conserved subcellular structure termed cytoophidium. In budding yeast, there are two isoforms of CTP synthase and both isoforms localize in cytoophidium. However, little is known about the distribution of CTP synthase isoforms in Drosophila melanogaster. Here, we report that three transcripts generated at the CTP synthase gene locus exhibit different expression profiles, and three isoforms encoded by this gene locus show a distinct subcellular distribution. While isoform A localizes in the nucleus, isoform B distributes diffusely in the cytoplasm, and only isoform C forms the cytoophidium. In the two isoform C-specific mutants, cytoophidia disappear in the germline cells. Although isoform A does not localize to the cytoophidium, a mutation disrupting mostly isoform A expression results in the disassembly of cytoophidia. Overexpression of isoform C can induce the growth of the cytoophidium in a cell-autonomous manner. Ectopic expression of the cytoophidium-forming isoform does not cause any defect in the embryos. In addition, we identify that a small segment at the amino terminus of isoform C is necessary but not sufficient for cytoophidium formation. Finally, we demonstrate that an excess of the synthetase domain of CTP synthase disrupts cytoophidium formation. Thus, the study of multiple isoforms of CTP synthase in Drosophila provides a good opportunity to dissect the biogenesis and function of the cytoophidum in a genetically tractable organism.
format Online
Article
Text
id pubmed-3573105
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-35731052013-03-01 Only One Isoform of Drosophila melanogaster CTP Synthase Forms the Cytoophidium Azzam, Ghows Liu, Ji-Long PLoS Genet Research Article CTP synthase is an essential enzyme that plays a key role in energy metabolism. Several independent studies have demonstrated that CTP synthase can form an evolutionarily conserved subcellular structure termed cytoophidium. In budding yeast, there are two isoforms of CTP synthase and both isoforms localize in cytoophidium. However, little is known about the distribution of CTP synthase isoforms in Drosophila melanogaster. Here, we report that three transcripts generated at the CTP synthase gene locus exhibit different expression profiles, and three isoforms encoded by this gene locus show a distinct subcellular distribution. While isoform A localizes in the nucleus, isoform B distributes diffusely in the cytoplasm, and only isoform C forms the cytoophidium. In the two isoform C-specific mutants, cytoophidia disappear in the germline cells. Although isoform A does not localize to the cytoophidium, a mutation disrupting mostly isoform A expression results in the disassembly of cytoophidia. Overexpression of isoform C can induce the growth of the cytoophidium in a cell-autonomous manner. Ectopic expression of the cytoophidium-forming isoform does not cause any defect in the embryos. In addition, we identify that a small segment at the amino terminus of isoform C is necessary but not sufficient for cytoophidium formation. Finally, we demonstrate that an excess of the synthetase domain of CTP synthase disrupts cytoophidium formation. Thus, the study of multiple isoforms of CTP synthase in Drosophila provides a good opportunity to dissect the biogenesis and function of the cytoophidum in a genetically tractable organism. Public Library of Science 2013-02-14 /pmc/articles/PMC3573105/ /pubmed/23459760 http://dx.doi.org/10.1371/journal.pgen.1003256 Text en © 2013 Azzam, Liu http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Azzam, Ghows
Liu, Ji-Long
Only One Isoform of Drosophila melanogaster CTP Synthase Forms the Cytoophidium
title Only One Isoform of Drosophila melanogaster CTP Synthase Forms the Cytoophidium
title_full Only One Isoform of Drosophila melanogaster CTP Synthase Forms the Cytoophidium
title_fullStr Only One Isoform of Drosophila melanogaster CTP Synthase Forms the Cytoophidium
title_full_unstemmed Only One Isoform of Drosophila melanogaster CTP Synthase Forms the Cytoophidium
title_short Only One Isoform of Drosophila melanogaster CTP Synthase Forms the Cytoophidium
title_sort only one isoform of drosophila melanogaster ctp synthase forms the cytoophidium
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3573105/
https://www.ncbi.nlm.nih.gov/pubmed/23459760
http://dx.doi.org/10.1371/journal.pgen.1003256
work_keys_str_mv AT azzamghows onlyoneisoformofdrosophilamelanogasterctpsynthaseformsthecytoophidium
AT liujilong onlyoneisoformofdrosophilamelanogasterctpsynthaseformsthecytoophidium