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Journal: bioRxiv
Article Title: STING causes replication stress and nascent DNA degradation via SAMHD1
doi: 10.64898/2026.03.28.714577
Figure Lengend Snippet: ( A ) Representative images of PLA on HDF shows STING-Lamin A interaction (foci) in control and progerin (PG)-expressing cells. DAPI is shown labeling genomic DNA. ( B ) Immunofluorescence analysis of BrdU incorporation in HDF treated with vehicle or doxycycline (Doxy) for 4 or 8 days to induce GFP-progerin, with or without STING inhibitor H151. ( C ) BrdU incorporation in HDF and progerin-expressing HDF transfected with STING siRNA (siSTING) or non-targeting control (siSCR). ( D ) Immunoblot analysis of STING, GFP-progerin, and phosphorylated RPA ( S33 p-RPA) in HDF control and progerin-expressing HDF in which STING is abrogated (H151 or siSTING). ( E ) IF images showing S33 p-RPA foci (red) in cells treated with Doxy ± H151 for 4 or 8 days; DAPI (blue) labels nuclei and white arrows indicate cytosolic foci. Scale bars, 20 µm ( F ) Quantification of cells with ≥3 nuclear S33 p-RPA foci per nucleus from (E). ( G ) Quantification of cells with nuclear S33 p-RPA foci in siSTING-or control siSCR-transfected cells treated with Doxy for 8 days. ( H ) Percentage of cells showing with ≥3 cytosolic S33 p-RPA foci from (E). ( I ) Cytosolic S33 p-RPA foci quantification in siSTING versus siSCR-transfected cells.
Article Snippet: Immunofluorescence was performed to analyze STING localization and activation (STING 1:500-Cell Signaling- 13647, S366 pSTING 1:1200- Cell Signaling-50907),
Techniques: Control, Expressing, Labeling, Immunofluorescence, BrdU Incorporation Assay, Transfection, Western Blot