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Assembly of IMPDH2-Based,CTPS-Based,and Mixed Rod/Ring Structures Is Dependent on Cell Type and Conditions of Induction 被引量:3

Assembly of IMPDH2-Based,CTPS-Based,and Mixed Rod/Ring Structures Is Dependent on Cell Type and Conditions of Induction
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摘要 Inhibition of guanosine triphosphate(GTP) and cytidine triphosphate(CTP) biosynthetic pathways induces cells to assemble rod/ring(RR) structures,also named cytoophidia,which consist of the enzymes cytidine triphosphate synthase(CTPS) and inosine-50-monophosphate dehydrogenase 2(IMPDH2).We aim to explore the interaction of CTPS and IMPDH2 in the generation of RR structures.He La and COS-7 cells were cultured in normal conditions or in the presence of 6-diazo-5-oxo-L-norleucine(DON),ribavirin,or mycophenolic acid(MPA).Over 90% of DON-treated cells presented RR structures.In He La cells,35% of the RR structures were positive for IMPDH2 alone,26% were CTPS alone,and 31% were IMPDH2/CTPS mixed,while in COS-7 cells,42% of RR were IMPDH2 alone,41% were CTPS alone,and 10% were IMPDH2/CTPS mixed.Ribavirin and MPA treatments induced only IMPDH2-based RR.Cells were also transfected with an N-terminal hemagglutinin(NHA)-tagged CTPS1 construct.Over 95% of NHA-CTPS1 transfected cells with DON treatment presented IMPDH2-based RR and almost 100% presented CTPS1-based RR;when treated with ribavirin,over 94% of transfected cells presented IMPDH2-based RR and 37% presented CTPS1-based RR,whereas 2% of untreated transfected cells presented IMPDH2-based RR and 28% presented CTPS1-based RR.These results may help in understanding the relationship between CTP and GTP biosynthetic pathways,especially concerning the formation of filamentous RR structures. Inhibition of guanosine triphosphate(GTP) and cytidine triphosphate(CTP) biosynthetic pathways induces cells to assemble rod/ring(RR) structures,also named cytoophidia,which consist of the enzymes cytidine triphosphate synthase(CTPS) and inosine-50-monophosphate dehydrogenase 2(IMPDH2).We aim to explore the interaction of CTPS and IMPDH2 in the generation of RR structures.He La and COS-7 cells were cultured in normal conditions or in the presence of 6-diazo-5-oxo-L-norleucine(DON),ribavirin,or mycophenolic acid(MPA).Over 90% of DON-treated cells presented RR structures.In He La cells,35% of the RR structures were positive for IMPDH2 alone,26% were CTPS alone,and 31% were IMPDH2/CTPS mixed,while in COS-7 cells,42% of RR were IMPDH2 alone,41% were CTPS alone,and 10% were IMPDH2/CTPS mixed.Ribavirin and MPA treatments induced only IMPDH2-based RR.Cells were also transfected with an N-terminal hemagglutinin(NHA)-tagged CTPS1 construct.Over 95% of NHA-CTPS1 transfected cells with DON treatment presented IMPDH2-based RR and almost 100% presented CTPS1-based RR;when treated with ribavirin,over 94% of transfected cells presented IMPDH2-based RR and 37% presented CTPS1-based RR,whereas 2% of untreated transfected cells presented IMPDH2-based RR and 28% presented CTPS1-based RR.These results may help in understanding the relationship between CTP and GTP biosynthetic pathways,especially concerning the formation of filamentous RR structures.
出处 《Journal of Genetics and Genomics》 SCIE CAS CSCD 2015年第6期287-299,共13页 遗传学报(英文版)
基金 supported by the Brazilian Government Research Foundation CAPES (Coordination for the Improvement of Higher Education Personnel,No.9028-11-0) the Sao Paulo State Research Foundation (Sao Paulo Government agency FAPESP,No.2011/12448-0) both granted to LECA and GDK,and by the research grant from Brazilian Government Agency CNPq (No.305064/2011-8) to LECA
关键词 Nucleotide synthesis Enzyme aggregation Enzyme inhibition IMPDH2 CTPS Nucleotide synthesis Enzyme aggregation Enzyme inhibition IMPDH2 CTPS
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  • 1Abu-Baker, A., and Rouleau, G.A. (2007). Oculopharyngeal muscular dystrophy: recent advances in the understanding of the molecular pathogenic mechanisms and treatment strategies. Biochim. Biophys. Acta 1772: 173-185.
  • 2Alberts, B., Johnson, A., Lewis, J., Raft, M., Roberts, K., and Walter, P. (2008). Molecular Biology of the Cell, 5th Edition. (New York/Abingdon: Garland Science, Taylor & Francis Group).
  • 3Buszczak, M., Paterno, S., Lighthouse, D., Bachman, J., Planck, J., Owen, S., Skora, A.D., Nystul, T.G, Ohlstein, B., Allen, A., Wilhelm, J.E., Murphy, T.D., Levis, R.W., Matunis, E., Srivali, N., Hoskins, R.A., and Spradlmg, A.C. (2007). The carnegie protein trap library: a versatile tool for Drosophila developmental studies. Genetics 175: 1505-1531.
  • 4Calado, A., Tome, F.M., Brais, B., Rouleau, G.A., Kuhn, U., Wahle, E.,and Carmo-Fonseea, M. (2000). Nuclear inclusions in bculopharyngeal muscular dystrophy consist of poly(A) binding protein 2 aggregates which sequester poly(A) RNA. Hum. Mol. Genet. 9: 2321-2328.
  • 5Chang, YoF., and Carman, G.M. (2008). CTP synthetase and its role in phospholipid synthesis in the yeast Saccharomyces cerevisiae. Prog. Lipid Res. 47: 333-339.
  • 6Dej, K.J., and Spradllng, A.C. (1999). The endocycle controls nurse cell polytene chromosome structure during Drosophila oogenesis. Development 126: 293-303.
  • 7Dix, C.I., and Raff, J.W. (2007). Drosophila Spd-2 recruits PCM to the sperm centriole, but is dispensable for centriole duplication. Curr. Biol. 17: 1759-1764.
  • 8Glick, B.S., and Nakano, A. (2009). Membrane traffic within the Golgi apparatus. Annu. Rev. Cell Dev. Biol. 25: 113-132.
  • 9Higgins, MJ., Loiselle, D., Haystead, T.A., and Graves, L.M. (2008). Human cytidine triphosphate synthetase 1 interacting proteins. Nucleosides Nucleotides Nucleic Acids 27: 850-857.
  • 10Kent, C., and Carman, G.M. (1999). Interactions among pathways for phosphatidylcholine metabolism, CTP synthesis and secretion through the Golgi apparatus. Trends Biochem. Sci. 24: 146-150.

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