scholarly journals CTP synthase does not form cytoophidia in Drosophila interfollicular stalks

2021 ◽  
Author(s):  
Zheng Wu ◽  
Ji-Long Liu
Keyword(s):  
De Novo ◽  
In Vivo Study ◽  
Follicle Cells ◽  
De Novo Synthesis ◽  
Ctp Synthase ◽  
Domains Of Life ◽  
Different Populations ◽  
Germline Cells

ABSTRACTCTP synthase (CTPS) catalyzes the final step of de novo synthesis of the nucleotide CTP. In 2010, CTPS has been found to form filamentous structures termed cytoophidia in Drosophila follicle cells and germline cells. Subsequently, cytoophidia have been reported in many species across three domains of life: bacteria, eukaryotes and archaea. Forming cytoophidia appears to be a highly conserved and ancient property of CTPS. To our surprise, here we find that polar cells and stalk cells, two specialized types of cells composing Drosophila interfollicular stalks, do not possess obvious cytoophidia. Moreover, we show that Myc level is low in these two types of cells, supporting the idea that Myc regulates cytoophidium assembly. Treatment with a glutamine analog, 6-diazo-5-oxo-l-norleucine (DON), increases cytoophidium assembly in main follicle cells, but not in polar cells or stalk cells. Our findings provide an interesting paradigm for the in vivo study of cytoophidium assembly and disassembly among different populations of follicle cells.

scholarly journals CTP synthase forms cytoophidia in archaea

2019 ◽  
Author(s):  
Shuang Zhou ◽  
Hua Xiang ◽  
Ji-Long Liu
Keyword(s):  
De Novo ◽  
Stimulated Emission ◽  
Metabolic Enzyme ◽  
De Novo Synthesis ◽  
Low Salt ◽  
Ctp Synthase ◽  
Intracellular Compartments ◽  
Domains Of Life ◽  
Haloarcula Hispanica ◽  
Rate Limiting

AbstractCTP synthase (CTPS) is an important metabolic enzyme that catalyzes the rate-limiting reaction of de novo synthesis of the nucleotide CTP. Since 2010, a series of studies have demonstrated that CTPS can form filamentous structures termed cytoophidia in bacteria and eukaryotes. However, it remains unknown whether cytoophidia exist in archaea, the third domain of life. Using Haloarcula hispanica as a model system, here we demonstrate that CTPS forms distinct intracellular compartments in archaeal cells. Under stimulated emission depletion (STED) microscopy, we find that some HhCTPS compartments have elongated filamentous structures, resembling cytoophidia in bacteria and eukaryotes. When Haloarcula cells are cultured in low-salt medium, the occurrence of cytoophidia increases dramatically. Moreover, overexpression of CTPS or glutamine analog treatment promotes cytoophidium assembly in H. hispanica. Our study reveals that CTPS forms cytoophidia in all three domains of life, suggesting that this is an ancient property of CTPS.

Divergent effects of intravenous GSH and cysteine on renal and hepatic GSH

1992 ◽  
Vol 263 (2) ◽  
pp. R348-R352 ◽  
Author(s):  
S. Aebi ◽  
B. H. Lauterburg
Keyword(s):  
Steady State ◽  
De Novo ◽  
Feedback Inhibition ◽  
Therapeutic Use ◽  
Steady State Concentration ◽  
De Novo Synthesis ◽  
State Concentration ◽  
Cellular Thiol

There is a growing interest in the therapeutic use of sulfhydryls. To assess the effect of glutathione (GSH) and cysteine on the cellular thiol status, thiols were administered intravenously to rats in doses ranging from 1.67 to 8.35 mmol/kg with and without pretreatment with 4 mmol/kg buthionine-[S,R]-sulfoximine (BSO), an inhibitor of GSH synthesis. One hour after administration of 1.67 mmol/kg GSH, the concentration of GSH rose from 5.2 +/- 1.0 to 8.4 +/- 0.9 mumol/g and from 2.5 +/- 0.5 to 3.7 +/- 0.7 mumol/g in liver and kidneys, respectively. After 8.35 mmol/kg, hepatic GSH did not increase further, but renal GSH rose to 6.7 +/- 1.8 mumol/g. Infusion of cysteine increased hepatic GSH to the same extent as intravenous GSH, but renal GSH did not increase after 1.67 mmol/kg and even significantly decreased to 0.6 +/- 0.2 mumol/g after 8.35 mmol/kg. In the presence of BSO, GSH resulted in a significant increase in renal but not hepatic GSH, suggesting that the kidneys take up intact GSH and indicating that the increment in hepatic GSH was due to de novo synthesis. The present data show that hepatic GSH can be markedly increased in vivo by increasing the supply of cysteine. Measurements of hepatic cysteine indicate that up to a concentration of approximately 0.5 mumol/g cysteine is a key determinant of hepatic GSH, such that the physiological steady-state concentration of GSH in the liver appears to be mainly determined by the availability of cysteine. At higher concentrations GSH does not increase further, possibly due to feedback inhibition of GSH synthesis or increased efflux.(ABSTRACT TRUNCATED AT 250 WORDS)

scholarly journals Transcriptional signatures of somatic neoblasts and germline cells in Macrostomum lignano

eLife ◽  
2016 ◽  
Vol 5 ◽  
Author(s):  
Magda Grudniewska ◽  
Stijn Mouton ◽  
Daniil Simanov ◽  
Frank Beltman ◽  
Margriet Grelling ◽  
...  
Keyword(s):  
Gene Expression ◽  
Stem Cells ◽  
De Novo ◽  
Transcriptome Assembly ◽  
Model Organism ◽  
Proliferating Cells ◽  
Macrostomum Lignano ◽  
Germline Cells

The regeneration-capable flatworm Macrostomum lignano is a powerful model organism to study the biology of stem cells in vivo. As a flatworm amenable to transgenesis, it complements the historically used planarian flatworm models, such as Schmidtea mediterranea. However, information on the transcriptome and markers of stem cells in M. lignano is limited. We generated a de novo transcriptome assembly and performed the first comprehensive characterization of gene expression in the proliferating cells of M. lignano, represented by somatic stem cells, called neoblasts, and germline cells. Knockdown of a selected set of neoblast genes, including Mlig-ddx39, Mlig-rrm1, Mlig-rpa3, Mlig-cdk1, and Mlig-h2a, confirmed their crucial role for the functionality of somatic neoblasts during homeostasis and regeneration. The generated M. lignano transcriptome assembly and gene expression signatures of somatic neoblasts and germline cells will be a valuable resource for future molecular studies in M. lignano.

scholarly journals De Novo Synthesis of VP16 Coordinates the Exit from HSV Latency In Vivo

2009 ◽  
Vol 5 (3) ◽  
pp. e1000352 ◽  
Author(s):  
Richard L. Thompson ◽  
Chris M. Preston ◽  
Nancy M. Sawtell
Keyword(s):  
De Novo ◽  
De Novo Synthesis

scholarly journals Correction: A ratiometric fluorescent probe for peroxynitrite prepared by de novo synthesis and its application in assessing the mitochondrial oxidative stress status in cells and in vivo

2018 ◽  
Vol 54 (93) ◽  
pp. 13159-13159 ◽  
Author(s):  
Dong-Ye Zhou ◽  
Yongfei Li ◽  
Wen-Li Jiang ◽  
Yang Tian ◽  
Junjie Fei ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Fluorescent Probe ◽  
De Novo ◽  
De Novo Synthesis ◽  
Mitochondrial Oxidative Stress ◽  
Oxidative Stress Status ◽  
Ratiometric Fluorescent Probe ◽  
In Cells

Correction for ‘A ratiometric fluorescent probe for peroxynitrite prepared by de novo synthesis and its application in assessing the mitochondrial oxidative stress status in cells and in vivo’ by Dong-Ye Zhou et al., Chem. Commun., 2018, 54, 11590–11593.

Screening of Basidiomycetes and Ascomycetes for Plant Growth Regulating Substances. Introduction of the Gibberellic Acid Induced de-novo Synthesis of Hydrolytic Enzymes in Embryoless Seeds of Triticum aestivum as Test System

1990 ◽  
Vol 45 (11-12) ◽  
pp. 1093-1098 ◽  
Author(s):  
Ralf Hautzel ◽  
Heidrun Anke
Keyword(s):  
Triticum Aestivum ◽  
Plant Growth ◽  
Gibberellic Acid ◽  
De Novo ◽  
Hydrolytic Enzymes ◽  
Test System ◽  
Active Principle ◽  
De Novo Synthesis ◽  
Plant Growth Regulating Substances

Abstract A new test system for the detection of plant growth regulating activities was successfully employed. In a screening for inhibitors of the gibberellic acid controlled synthesis of hydrolytic enzymes in embryoless wheat seeds (Triticum aestivum) 160 cultures of ascomycetes and basi­diomycetes were tested. In the extracts of two cultures inhibitory activities were detected. From fermentations of a Hypholoma-species (basidiomycetes) 3,5-dichloro-4-methoxybenzyl alcohol was isolated as the active principle. Galiellalactone and two other new phytotoxins were isolated from cultures of the ascomycete Galiella rufa. At concentrations of 50 μg/ml all four compounds inhibited the de-novo synthesis of α-amylases, proteases, and phosphatases. Further investigations on the mode of action revealed, that all four metabolites interfere with early steps of the biosynthetic path­ ways induced by gibberellic acids. In vivo, the germination of the seeds of several plants was inhibited by these compounds.

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