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Bethyl
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Journal: bioRxiv
Article Title: RNA polymerase loss by nuclear rupture drives LMNA cardiomyopathy
doi: 10.64898/2026.04.03.716433
Figure Lengend Snippet: A) Immunofluorescence for gamma-H2AX in cardiomyocytes expressing NLS-tdTomato and GFP-icGAS isolated from mice at day 14 post tamoxifen. Texts and icons below images indicate nuclear states. Scale bar: 5 μm. B) Nuclear gamma-H2AX intensity by nuclear states. Density and box plots (interquartile range): signal distribution of all affiliated nuclei. Circles: mean intensity within individual biological replicates (color coded). Statistics: P < 0.05 (*) or P≥0.05 (N.S.) from t-tests on linear regression-estimated means with mouse-clustered standard errors. Underlying data: 164 intact nuclei from 3 WT mice, 152 intact, 116 ruptured, 50 resealed nuclei from 3 Lmna CKO mice. C) Relationship between gamma-H2AX intensity and NLS-tdTomato intensity in nuclei of Lmna CKO cardiomyocytes (340 nuclei from 3 mice). Line: simple linear regression fit with 95% confidence interval. R: Pearson’s correlation coefficient. P: t-test p -value on linear regression-estimated means with mouse-clustered standard errors.
Article Snippet:
Techniques: Immunofluorescence, Expressing, Isolation
Journal: EMBO Reports
Article Title: Inhibition of the minor spliceosome restricts the growth of a broad spectrum of cancers
doi: 10.1038/s44319-025-00511-8
Figure Lengend Snippet: ( A ) RT-PCR analysis of MIG splicing changes in A549 cells after 72 h treatment with 10 nM ASO. Schematic depictions of the obtained amplicons are shown on the right with the minor intron in red and the upstream and downstream exons coloured blue and orange, respectively. Exons not separated by a minor intron are grey. ( B ) Representative images of γH2Ax (Ser139) staining in A549 cells 72 h after 10 nM ASO treatment. Scale bar is 10 µm.
Article Snippet: IF
Techniques: Reverse Transcription Polymerase Chain Reaction, Staining
Journal: Advanced Functional Materials
Article Title: Alleviation of Aging‐Related Hallmarks in a Mouse Model of Progeria via a Nanoparticle‐Based Artificial Transcription Factor
doi: 10.1002/adfm.202425944
Figure Lengend Snippet: Figure 4. Amelioration of aging-associated hallmarks in LMNA G608G cells via Oct4-nanoscript. A) Immunofluorescence for Oct4+ and H3K9me3+ cells in control and LMNAG/G fibroblasts with or without Oct4-nanoscript. Scale bar = 20 μm. B) Quantification of the fluorescence intensity of H3K9me3 in nuclei using a single confocal section. Data represent mean ± SEM. Two-way ANOVA-test, *P < 0.05, **P < 0.01; n = 12 from three samples per group. C) The relative intensity of H3K9me3 levels in control and LMNAG/G fibroblasts treated with Oct4-nanoscript. Data represent mean ± SEM. Two-way ANOVA-test, **P < 0.01; n = 3 per group. D,E) Western blot analysis of 𝛾-H2AX and total histone H3 in control and LMNAG/G fibroblasts treated with
Article Snippet: The cells were incubated overnight at 4 °C with following primary antibodies: anti-Oct4 (Abcam, ab18976; Santacruz, sc-5279), anti-H3K9me3 (Abcam, ab8898), anti-H4K20me3 (Abcam, ab78517),
Techniques: Control, Western Blot