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Mutations in the NR4A2 LBD result in mis-localisation of the receptor with DNA repair proteins.

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posted on 2013-11-06, 03:25 authored by Kasturee Jagirdar, Kelvin Yin, Matthew Harrison, Wen Lim, George E. O. Muscat, Richard A. Sturm, Aaron G. Smith

(A) Schematic representation of the WT and ΔH12 mutant forms of NR4A2 indicating the position of the C-terminal helix 12. MM96L cells transfected with WT or ΔH12 forms of NR4A2 were treated with 25 mJ/cm2 UV, fixed at 4 hours post-UV treatment. Immunofluorescence was performed to detect (B) γH2A.X; (C) DDB2; and (D) XPC proteins. Left panels (green fluorescence), pEYFP-NR4A-WT (upper) or pEYFP-NR4A2-ΔH12 (lower); Middle panels, γH2A.X, DDB2 or XPC immunofluorescence (red); Right panels, merged images; Representative images from 4 independent experiments is shown.

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