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Image Search Results
Journal: Molecular cell
Article Title: The nucleolar granular component mediates genome-nucleolus interactions and establishes their repressive chromatin states.
doi: 10.1016/j.molcel.2025.05.004
Figure Lengend Snippet: Figure 2. NPM1 associates with NADs (A) Integrative genomics viewer (IGV) track displaying NPM1 genome occupancy and NAD profiles from nucleolar-DamID11 of chromosome 5 in mESCs. (B) Genomic annotations of NPM1-bound regions at NAD and non-NADs of mESCs. Promoter corresponds to ±3 kb regions from transcription start sites. (C) NPM1 distribution on NADs and LAD-only sequences in mESCs. (D) Volcano plot showing fold change (log2 values) in transcript levels of mESCs + siRNA-Npm1 vs. mESC + siRNA-control. Gene expression values of three replicates were averaged and selected for 1.5-fold changes and p < 0.05. (E) Top 10 Gene Ontology (GO) terms as determined using database for annotation, visualization, and integrated discovery (DAVID) for genes upregulated and downregulated upon NPM1-KD. (F) Pie chart showing the number of genes located at NAD-only and NAD/LAD regions that are significantly upregulated or downregulated in mESC upon NPM1-KD.
Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER Experimental models: Cell lines One hundred and twenty-nine mouse embryonic stem cells (E14 line) Savi�c et al.40 N/A HEK293T ATCC N/A NIH3T3 ATCC N/A HP1α/β-cDKO mESC Ballmer et al.24 N/A hsp-TetO-H2B-Dam-NoLS-DD mESCs Bersaglieri et al.11 N/A FLAG-HA-NPM1 mESCs This work N/A FKBP-NPM1 mESCs This work N/A Oligonucleotides Oligonucleotides for qPCR and siRNA This work Table S7 Recombinant DNA Super PiggyBac Transposase Expression Vector SBI System Biosciences PB210PA-1 pSpCas9(BB)-2A-GFP Addgene 48138 pX330 Mouse 5’
Techniques: Control, Gene Expression
Journal: Molecular cell
Article Title: The nucleolar granular component mediates genome-nucleolus interactions and establishes their repressive chromatin states.
doi: 10.1016/j.molcel.2025.05.004
Figure Lengend Snippet: Figure 3. NPM1 regulates G9a-mediated H3K9me2 at NADs (A) Representative immunofluorescence images showing H3K9me2 distribution in mESCs treated with siRNA-control or siRNA-Npm1. The magnification on the right shows the distribution of H3K9me2 around nucleoli, forming a ring-like shape that is destroyed in the absence of NPM1. Upstream binding transcription factor (UBF) serves as a nucleolar marker. Scale bar represents 5 μm. The corresponding DAPI staining is shown in Figure S3F. (B) Quantification of cells showing the perinucleolar H3K9me2 ring in mESCs upon depletion of G9a, SUV39H1/2, or SETDB1. Data are from three independent experiments. Error bars represent SD. Statistical significance (p values) was calculated using the Mann-Whitney test (***p < 0.001).
Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER Experimental models: Cell lines One hundred and twenty-nine mouse embryonic stem cells (E14 line) Savi�c et al.40 N/A HEK293T ATCC N/A NIH3T3 ATCC N/A HP1α/β-cDKO mESC Ballmer et al.24 N/A hsp-TetO-H2B-Dam-NoLS-DD mESCs Bersaglieri et al.11 N/A FLAG-HA-NPM1 mESCs This work N/A FKBP-NPM1 mESCs This work N/A Oligonucleotides Oligonucleotides for qPCR and siRNA This work Table S7 Recombinant DNA Super PiggyBac Transposase Expression Vector SBI System Biosciences PB210PA-1 pSpCas9(BB)-2A-GFP Addgene 48138 pX330 Mouse 5’
Techniques: Immunofluorescence, Control, Binding Assay, Marker, Staining, MANN-WHITNEY