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The hexosamine biosynthesis pathway and O-GlcNAcylation. GFAT, L-glutamine: fructose-6-phosphate amidotransferase; OGT, O-GlcNAc transferase; <t>OGA,</t> O-GlcNAcase; <t>UDP-GlcNAc,</t> <t>UDP-N-acetylglucosamine;</t> NAGK, N acetyl-glucosamine kinase
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The hexosamine biosynthesis pathway and O-GlcNAcylation. GFAT, L-glutamine: fructose-6-phosphate amidotransferase; OGT, O-GlcNAc transferase; OGA, O-GlcNAcase; UDP-GlcNAc, UDP-N-acetylglucosamine; NAGK, N acetyl-glucosamine kinase

Journal: BMC Molecular and Cell Biology

Article Title: Sex alters thyroid hormone’s effect on protein O -GlcNAcylation in the aged mouse heart

doi: 10.1186/s12860-025-00543-x

Figure Lengend Snippet: The hexosamine biosynthesis pathway and O-GlcNAcylation. GFAT, L-glutamine: fructose-6-phosphate amidotransferase; OGT, O-GlcNAc transferase; OGA, O-GlcNAcase; UDP-GlcNAc, UDP-N-acetylglucosamine; NAGK, N acetyl-glucosamine kinase

Article Snippet: The primary antibodies used in this study were as follows: anti-O-linked N-acetylglucosamine [RL2] (#ab2730, Abcam, Cambridge, UK), OGT(#ab96718, Abcam, Cambridge, UK), OGA (#NBP1-81244, Novus Biologicals, Centennial, CO), GFAT1 (#NBP3-04455, Novus Biologicals, Centennial, CO), GFAT2 (#sc-134710, Santa Cruz Biotechnologies, Dallas, TX) and NAGK (#15051-1-AP, Proteintech, Rosemont, IL).The secondary antibodies used in this study was goat anti-mouse IgG, light chain specific (#115-035-174, Jackson ImmunoResearch, West Grove PA) and goat anti-rabbit IgG (H + L) (#1706515, Bio-Rad, Hercules, CA).

Techniques:

ACAA2/TRβ1 transcriptional assay. Inhibiting O-GlcNAc in transfected TH-treated CV-1 cells reduced ACAA2 activation of TRβ1 transcriptional activity. TRβ1 – thyroid receptor β1; ACAA2 – acetyl-coenzyme A acyltransferase; T3 – thyroid hormone; TG – thiamet G, OGA inhibitor; OSMI-1 – OGT inhibitor. Statistics – one-way ANOVA – correct for multiple comparison- test: Šidák post hoc analysis was performed (n = 4).

Journal: BMC Molecular and Cell Biology

Article Title: Sex alters thyroid hormone’s effect on protein O -GlcNAcylation in the aged mouse heart

doi: 10.1186/s12860-025-00543-x

Figure Lengend Snippet: ACAA2/TRβ1 transcriptional assay. Inhibiting O-GlcNAc in transfected TH-treated CV-1 cells reduced ACAA2 activation of TRβ1 transcriptional activity. TRβ1 – thyroid receptor β1; ACAA2 – acetyl-coenzyme A acyltransferase; T3 – thyroid hormone; TG – thiamet G, OGA inhibitor; OSMI-1 – OGT inhibitor. Statistics – one-way ANOVA – correct for multiple comparison- test: Šidák post hoc analysis was performed (n = 4).

Article Snippet: The primary antibodies used in this study were as follows: anti-O-linked N-acetylglucosamine [RL2] (#ab2730, Abcam, Cambridge, UK), OGT(#ab96718, Abcam, Cambridge, UK), OGA (#NBP1-81244, Novus Biologicals, Centennial, CO), GFAT1 (#NBP3-04455, Novus Biologicals, Centennial, CO), GFAT2 (#sc-134710, Santa Cruz Biotechnologies, Dallas, TX) and NAGK (#15051-1-AP, Proteintech, Rosemont, IL).The secondary antibodies used in this study was goat anti-mouse IgG, light chain specific (#115-035-174, Jackson ImmunoResearch, West Grove PA) and goat anti-rabbit IgG (H + L) (#1706515, Bio-Rad, Hercules, CA).

Techniques: Transcription Assay, Transfection, Activation Assay, Activity Assay, Comparison