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(A) The AlphaFold3 predicted DNA-protein complex with I. scapularis Nrf2 (dark purple), I. scapularis MafG (light purple), and the predicted promoter of nup214 (yellow). DNA binding residues are highlighted in green and the consensus binding site is indicated in orange. (B) nup214 expression quantified from A. phagocytophilum infected IDE12 tick cells treated with siRNA targeting nrf2 or a scrambled control. (C) nup214 expression quantified from A. phagocytophilum infected ISE6 cells treated with siRNA targeting keap1 or a scrambled control. (D-E) HEK 293T cells were co-transfected with plasmids constitutively expressing I. scapularis Nrf2 and (D) a <t>luciferase</t> reporter plasmid with the I. scapularis nup214 promoter or (E) a luciferase reporter plasmid with a mutated I. scapularis nup214 promoter. Luciferase activity was normalized to the condition with only the luciferase reporter plasmid transfected. RLU is relative luminescence units. *, P < 0.05 (Student’s t test). scRNA, scrambled RNA; siRNA, small interfering RNA.
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(A) The AlphaFold3 predicted DNA-protein complex with I. scapularis Nrf2 (dark purple), I. scapularis MafG (light purple), and the predicted promoter of nup214 (yellow). DNA binding residues are highlighted in green and the consensus binding site is indicated in orange. (B) nup214 expression quantified from A. phagocytophilum infected IDE12 tick cells treated with siRNA targeting nrf2 or a scrambled control. (C) nup214 expression quantified from A. phagocytophilum infected ISE6 cells treated with siRNA targeting keap1 or a scrambled control. (D-E) HEK 293T cells were co-transfected with plasmids constitutively expressing I. scapularis Nrf2 and (D) a <t>luciferase</t> reporter plasmid with the I. scapularis nup214 promoter or (E) a luciferase reporter plasmid with a mutated I. scapularis nup214 promoter. Luciferase activity was normalized to the condition with only the luciferase reporter plasmid transfected. RLU is relative luminescence units. *, P < 0.05 (Student’s t test). scRNA, scrambled RNA; siRNA, small interfering RNA.
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(A) The AlphaFold3 predicted DNA-protein complex with I. scapularis Nrf2 (dark purple), I. scapularis MafG (light purple), and the predicted promoter of nup214 (yellow). DNA binding residues are highlighted in green and the consensus binding site is indicated in orange. (B) nup214 expression quantified from A. phagocytophilum infected IDE12 tick cells treated with siRNA targeting nrf2 or a scrambled control. (C) nup214 expression quantified from A. phagocytophilum infected ISE6 cells treated with siRNA targeting keap1 or a scrambled control. (D-E) HEK 293T cells were co-transfected with plasmids constitutively expressing I. scapularis Nrf2 and (D) a <t>luciferase</t> reporter plasmid with the I. scapularis nup214 promoter or (E) a luciferase reporter plasmid with a mutated I. scapularis nup214 promoter. Luciferase activity was normalized to the condition with only the luciferase reporter plasmid transfected. RLU is relative luminescence units. *, P < 0.05 (Student’s t test). scRNA, scrambled RNA; siRNA, small interfering RNA.
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(A) The AlphaFold3 predicted DNA-protein complex with I. scapularis Nrf2 (dark purple), I. scapularis MafG (light purple), and the predicted promoter of nup214 (yellow). DNA binding residues are highlighted in green and the consensus binding site is indicated in orange. (B) nup214 expression quantified from A. phagocytophilum infected IDE12 tick cells treated with siRNA targeting nrf2 or a scrambled control. (C) nup214 expression quantified from A. phagocytophilum infected ISE6 cells treated with siRNA targeting keap1 or a scrambled control. (D-E) HEK 293T cells were co-transfected with plasmids constitutively expressing I. scapularis Nrf2 and (D) a <t>luciferase</t> reporter plasmid with the I. scapularis nup214 promoter or (E) a luciferase reporter plasmid with a mutated I. scapularis nup214 promoter. Luciferase activity was normalized to the condition with only the luciferase reporter plasmid transfected. RLU is relative luminescence units. *, P < 0.05 (Student’s t test). scRNA, scrambled RNA; siRNA, small interfering RNA.
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(A) The AlphaFold3 predicted DNA-protein complex with I. scapularis Nrf2 (dark purple), I. scapularis MafG (light purple), and the predicted promoter of nup214 (yellow). DNA binding residues are highlighted in green and the consensus binding site is indicated in orange. (B) nup214 expression quantified from A. phagocytophilum infected IDE12 tick cells treated with siRNA targeting nrf2 or a scrambled control. (C) nup214 expression quantified from A. phagocytophilum infected ISE6 cells treated with siRNA targeting keap1 or a scrambled control. (D-E) HEK 293T cells were co-transfected with plasmids constitutively expressing I. scapularis Nrf2 and (D) a <t>luciferase</t> reporter plasmid with the I. scapularis nup214 promoter or (E) a luciferase reporter plasmid with a mutated I. scapularis nup214 promoter. Luciferase activity was normalized to the condition with only the luciferase reporter plasmid transfected. RLU is relative luminescence units. *, P < 0.05 (Student’s t test). scRNA, scrambled RNA; siRNA, small interfering RNA.
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Image Search Results


(A) The AlphaFold3 predicted DNA-protein complex with I. scapularis Nrf2 (dark purple), I. scapularis MafG (light purple), and the predicted promoter of nup214 (yellow). DNA binding residues are highlighted in green and the consensus binding site is indicated in orange. (B) nup214 expression quantified from A. phagocytophilum infected IDE12 tick cells treated with siRNA targeting nrf2 or a scrambled control. (C) nup214 expression quantified from A. phagocytophilum infected ISE6 cells treated with siRNA targeting keap1 or a scrambled control. (D-E) HEK 293T cells were co-transfected with plasmids constitutively expressing I. scapularis Nrf2 and (D) a luciferase reporter plasmid with the I. scapularis nup214 promoter or (E) a luciferase reporter plasmid with a mutated I. scapularis nup214 promoter. Luciferase activity was normalized to the condition with only the luciferase reporter plasmid transfected. RLU is relative luminescence units. *, P < 0.05 (Student’s t test). scRNA, scrambled RNA; siRNA, small interfering RNA.

Journal: bioRxiv

Article Title: An Nrf2-Nup214 positive feedback loop sustains the antioxidant response and promotes microbial infection in ticks

doi: 10.64898/2026.05.06.723311

Figure Lengend Snippet: (A) The AlphaFold3 predicted DNA-protein complex with I. scapularis Nrf2 (dark purple), I. scapularis MafG (light purple), and the predicted promoter of nup214 (yellow). DNA binding residues are highlighted in green and the consensus binding site is indicated in orange. (B) nup214 expression quantified from A. phagocytophilum infected IDE12 tick cells treated with siRNA targeting nrf2 or a scrambled control. (C) nup214 expression quantified from A. phagocytophilum infected ISE6 cells treated with siRNA targeting keap1 or a scrambled control. (D-E) HEK 293T cells were co-transfected with plasmids constitutively expressing I. scapularis Nrf2 and (D) a luciferase reporter plasmid with the I. scapularis nup214 promoter or (E) a luciferase reporter plasmid with a mutated I. scapularis nup214 promoter. Luciferase activity was normalized to the condition with only the luciferase reporter plasmid transfected. RLU is relative luminescence units. *, P < 0.05 (Student’s t test). scRNA, scrambled RNA; siRNA, small interfering RNA.

Article Snippet: The promoter sequences were cloned into a pTE luciferase reporter (Signosis, LR-2200) using BgIII.

Techniques: Binding Assay, Expressing, Infection, Control, Transfection, Luciferase, Plasmid Preparation, Activity Assay, Small Interfering RNA