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1.
Blood ; 141(18): 2245-2260, 2023 05 04.
Article in English | MEDLINE | ID: mdl-36735909

ABSTRACT

The NFIA-ETO2 fusion is the product of a t(1;16)(p31;q24) chromosomal translocation, so far, exclusively found in pediatric patients with pure erythroid leukemia (PEL). To address the role for the pathogenesis of the disease, we facilitated the expression of the NFIA-ETO2 fusion in murine erythroblasts (EBs). We observed that NFIA-ETO2 significantly increased proliferation and impaired erythroid differentiation of murine erythroleukemia cells and of primary fetal liver-derived EBs. However, NFIA-ETO2-expressing EBs acquired neither aberrant in vitro clonogenic activity nor disease-inducing potential upon transplantation into irradiated syngenic mice. In contrast, in the presence of 1 of the most prevalent erythroleukemia-associated mutations, TP53R248Q, expression of NFIA-ETO2 resulted in aberrant clonogenic activity and induced a fully penetrant transplantable PEL-like disease in mice. Molecular studies support that NFIA-ETO2 interferes with erythroid differentiation by preferentially binding and repressing erythroid genes that contain NFI binding sites and/or are decorated by ETO2, resulting in a activity shift from GATA- to ETS-motif-containing target genes. In contrast, TP53R248Q does not affect erythroid differentiation but provides self-renewal and survival potential, mostly via downregulation of known TP53 targets. Collectively, our work indicates that NFIA-ETO2 initiates PEL by suppressing gene expression programs of terminal erythroid differentiation and cooperates with TP53 mutation to induce erythroleukemia.


Subject(s)
Leukemia, Erythroblastic, Acute , Repressor Proteins , Animals , Mice , Repressor Proteins/genetics , Leukemia, Erythroblastic, Acute/genetics , Leukemia, Erythroblastic, Acute/metabolism , Cell Differentiation/genetics , Erythroblasts/metabolism , NFI Transcription Factors/metabolism
2.
EMBO Rep ; 23(11): e54025, 2022 11 07.
Article in English | MEDLINE | ID: mdl-36134875

ABSTRACT

Adenosine triphosphate (ATP) production and utilization is critically important for animal development. How these processes are regulated in space and time during tissue growth remains largely unclear. We used a FRET-based sensor to dynamically monitor ATP levels across a growing tissue, using the Drosophila larval wing disc. Although steady-state levels of ATP are spatially uniform across the wing pouch, inhibiting oxidative phosphorylation reveals spatial differences in metabolic behavior, whereby signaling centers at compartment boundaries produce more ATP from glycolysis than the rest of the tissue. Genetic perturbations indicate that the conserved Hedgehog signaling pathway can enhance ATP production by glycolysis. Collectively, our work suggests the existence of a homeostatic feedback loop between Hh signaling and glycolysis, advancing our understanding of the connection between conserved developmental patterning genes and ATP production during animal tissue development.


Subject(s)
Drosophila Proteins , Drosophila , Animals , Drosophila/genetics , Drosophila/metabolism , Hedgehog Proteins/genetics , Hedgehog Proteins/metabolism , Drosophila Proteins/genetics , Drosophila Proteins/metabolism , Adenosine Triphosphate/metabolism , Gene Expression Regulation, Developmental , Wings, Animal/metabolism , Glycolysis , Drosophila melanogaster/genetics , Drosophila melanogaster/metabolism
4.
EMBO J ; 39(21): e101767, 2020 11 02.
Article in English | MEDLINE | ID: mdl-33021744

ABSTRACT

Changes in cell metabolism and plasma membrane potential have been linked to shifts between tissue growth and differentiation, and to developmental patterning. How such changes mediate these effects is poorly understood. Here, we use the developing wing of Drosophila to investigate the interplay between cell metabolism and a key developmental regulator-the Hedgehog (Hh) signalling pathway. We show that reducing glycolysis both lowers steady-state levels of ATP and stabilizes Smoothened (Smo), the 7-pass transmembrane protein that transduces the Hh signal. As a result, the transcription factor Cubitus interruptus accumulates in its full-length, transcription activating form. We show that glycolysis is required to maintain the plasma membrane potential and that plasma membrane depolarization blocks cellular uptake of N-acylethanolamides-lipoprotein-borne Hh pathway inhibitors required for Smo destabilization. Similarly, pharmacological inhibition of glycolysis in mammalian cells induces ciliary translocation of Smo-a key step in pathway activation-in the absence of Hh. Thus, changes in cell metabolism alter Hh signalling through their effects on plasma membrane potential.


Subject(s)
Cell Membrane/metabolism , Glycolysis/genetics , Glycolysis/physiology , Hedgehog Proteins/genetics , Hedgehog Proteins/metabolism , Membrane Potentials/physiology , Signal Transduction/genetics , Signal Transduction/physiology , Animals , Animals, Genetically Modified , Biological Transport , Drosophila Proteins/metabolism , Drosophila melanogaster/genetics , Drosophila melanogaster/metabolism , Energy Metabolism , Gene Expression Regulation , Gene Expression Regulation, Developmental , Gene Knockdown Techniques , Gramicidin/therapeutic use , Lipoproteins , Membrane Proteins/metabolism , Mice , NIH 3T3 Cells , Smoothened Receptor/metabolism , Transcription Factors/metabolism , Wings, Animal/growth & development , Wings, Animal/pathology , Wings, Animal/physiology
5.
BMC Genomics ; 19(1): 537, 2018 Jul 13.
Article in English | MEDLINE | ID: mdl-30005604

ABSTRACT

BACKGROUND: The prothoracic gland (PG), the principal steroidogenic organ of insects, has been proposed as a model for steroid hormone biosynthesis and regulation. RESULTS: To validate the robustness of the model, we present an analysis of accumulated transcriptomic data from PGs of two model species, Drosophila melanogaster and Bombyx mori. We identify that the common core components of the model in both species are encoded by nine genes. Five of these are Halloween genes whose expression differs substantially between the PGs of these species. CONCLUSIONS: We conclude that the PGs can be a model for steroid hormone synthesis and regulation within the context of mitochondrial cholesterol transport and steroid biosynthesis but beyond these core mechanisms, gene expression in insect PGs is too diverse to fit in a context-specific model and should be analysed within a species-specific framework.


Subject(s)
Bombyx/genetics , Drosophila melanogaster/genetics , Endocrine Glands/metabolism , Models, Biological , Animals , Cholesterol/metabolism , Cyclic AMP/metabolism , Insect Proteins/genetics , Insect Proteins/metabolism , RNA/chemistry , RNA/isolation & purification , RNA/metabolism , Sequence Analysis, RNA , Signal Transduction/genetics , Transcriptome
6.
Sci Rep ; 6: 20229, 2016 Feb 05.
Article in English | MEDLINE | ID: mdl-26847502

ABSTRACT

Ecdysteroids secreted by the prothoracic gland (PG) cells of insects control the developmental timing of their immature life stages. These cells have been historically considered as carrying out a single function in insects, namely the biochemical conversion of cholesterol to ecdysteroids and their secretion. A growing body of evidence shows that PG cells receive multiple cues during insect development so we tested the hypothesis that they carry out more than just one function in insects. We characterised the molecular nature and developmental profiles of cell membrane receptors in PG cells of Bombyx mori during the final larval stage and determined what receptors decode nutritional, developmental and physiological signals. Through iterative approaches we identified a complex repertoire of cell membrane receptors that are expressed in intricate patterns and activate previously unidentified signal transduction cascades in PG cells. The expression patterns of some of these receptors explain precisely the mechanisms that are known to control ecdysteroidogenesis. However, the presence of receptors for the notch, hedgehog and wingless signalling pathways and the expression of innate immunity-related receptors such as phagocytosis receptors, receptors for microbial ligands and Toll-like receptors call for a re-evaluation of the role these cells play in insects.


Subject(s)
Endocrine Glands/metabolism , Insect Proteins/metabolism , Receptors, Cell Surface/metabolism , Animals , Bombyx/growth & development , Bombyx/metabolism , Cell Membrane/metabolism , Chromatography, High Pressure Liquid , Ecdysteroids/metabolism , Endocrine Glands/cytology , Insect Proteins/genetics , Larva/growth & development , Larva/metabolism , Life Cycle Stages , Proteome/analysis , Real-Time Polymerase Chain Reaction , Receptors, Cell Surface/genetics , Tandem Mass Spectrometry , Transcriptome
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