downstream cccagttaatatgcaccgaa 3  (Addgene inc)

Journal: Discover Oncology

Article Title: Spatial transcriptomics of urothelial carcinoma with basal/squamous differentiation identifies Galectin-7 as a specific marker of squamous lineage commitment

doi: 10.1007/s12672-026-04927-z

Figure Lengend Snippet: LGALS7 is selectively expressed in Ba/Sq differentiation and promotes squamous carcinoma cell proliferation. A The H&E image from Fig. B is shown again, with a red box indicating the region analyzed in this figure. Spatial transcriptomic maps display TP63 and LGALS7 expression patterns within the boxed region, corresponding to the UC–Ba/Sq interface. B Cluster-level expression of TP63 and LGALS7. C Immunohistochemistry (IHC) of the cystectomy specimen showing diffuse p63 positivity in both urothelial carcinoma (UC) and Ba/Sq-differentiated tumor components, and selective Galectin-7 expression restricted to Ba/Sq-differentiated tumor nests. Scale bars, 1 mm. D Western blot showing Galectin-7 expression across cancer cell lines (left), and immunofluorescence (IF) of SCaBER cells showing cytoplasmic localization (right). E Proliferation assay of SCaBER cells following LGALS7 knockdown

Article Snippet: This analysis revealed a sequential transcriptional trajectory: (i) CAF-rich stroma enriched in TGF-β and extracellular matrix programs; (ii) NGFR-high transitional epithelium at the UC–stroma interface; (iii) basal-like Ba/Sq-differentiated tumor nests expressing TP63 and its downstream effector LGALS7 (Galectin-7); and (iv) terminally keratinized Ba/Sq-differentiated tumor cores dominated by epidermal differentiation complex (EDC) genes.

Techniques: Expressing, Immunohistochemistry, Western Blot, Immunofluorescence, Proliferation Assay, Knockdown

Journal: bioRxiv

Article Title: Stage-dependent chromatin accessibility remodeling defines an architectural state in facioscapulohumeral muscular dystrophy myoblasts

doi: 10.64898/2026.03.06.710110

Figure Lengend Snippet: (A) Chromosome-wide distribution of differentially accessible regions across all human autosomes. Each horizontal track represents an individual chromosome, arranged from chromosome 1 to chromosome 22. Up-DARs are indicated in red and Down-DARs in teal. Black and gray segments represent cytogenetic bands (cytobands) along each chromosome. The positions of DARs are shown relative to chromosomal coordinates, illustrating their genome-wide distribution. (B) Volcano plot showing differential chromatin accessibility between FSHD and control primary human myoblasts. Each point represents an individual ATAC-seq peak. The x-axis shows the log₂ fold change in accessibility (FSHD/CTRL), and the y-axis shows the −log₁₀(FDR). Regions with significantly increased accessibility in FSHD (Up-DARs) are shown in red, and regions with significantly decreased accessibility (Down-DARs) are shown in teal. Vertical dashed lines indicate fold-change thresholds, and the horizontal dashed line indicates the statistical significance threshold. ( 1 =chr19:42663366-42663803; 2 =chr8:125236306-125237721; 3 =chr4:37517813-37518483; 4 =chr15:84909779-84910176; 5 =chr7:146872319-146873047; 6 =chr1:180272411-18027321; 7 =chr7:41837735-41842398; 8 =chr7:146578703-146579358; 9 =chr7:147089937-147090658; 63012 =chr7:37253326-37254866; 63013 =chr8:11514184-11516273; 63014 =chr5:55485814-55486163; 63015 =chr21:30704676-30707177; 63024 =chr8:11518982-11519321). (C) Volcano plot showing differential chromatin accessibility between FSHD and control myotubes, displayed as in panel B. Each point represents an individual ATAC-seq peak, with Up-DARs shown in red and Down-DARs shown in teal. ( 1 =chr7:76053318-76053881; 2 =chr1:16126339-16127460; 3 =chr10:131229506-131231084; 4 =chr22:21699861-21700117; 5 =chr14:2770953-2771283; 6 =chr9:80192322-80193046; 7 =chr8:11514182-11516352; 8 = chr11:221023-221287; 9 =chr3:69747056-69747802). (D) Genomic annotation of Up-DARs identified in human primary myoblasts (HPMs; total = 5,102). Peaks were classified based on genomic location relative to annotated gene features, including promoter, exon, intron, 5′ untranslated region (UTR), 3′ UTR, downstream region, and distal intergenic region. Percentages and absolute counts are indicated. (E) Genomic annotation of Down-DARs identified in HPMs (total = 7,491), classified according to genomic features as in panel C. (F) Genomic annotation of Up-DARs identified in myotubes (total = 74), categorized according to genomic features as described above. (G) Genomic annotation of Down-DARs identified in myotubes (total = 89), categorized according to genomic features as described above.

Article Snippet: Primary read processing and downstream ATAC-seq data analysis were performed by Macrogen (Seoul, South Korea).

Techniques: Genome Wide, Control

Journal: bioRxiv

Article Title: Stage-dependent chromatin accessibility remodeling defines an architectural state in facioscapulohumeral muscular dystrophy myoblasts

doi: 10.64898/2026.03.06.710110

Figure Lengend Snippet:

Article Snippet: Primary read processing and downstream ATAC-seq data analysis were performed by Macrogen (Seoul, South Korea).

Techniques:

Journal: bioRxiv

Article Title: Stage-dependent chromatin accessibility remodeling defines an architectural state in facioscapulohumeral muscular dystrophy myoblasts

doi: 10.64898/2026.03.06.710110

Figure Lengend Snippet: (A) TSS enrichment profile showing the distribution of ATAC-seq signal centered on annotated transcription start sites (TSS). The x-axis indicates the distance from the TSS (kb), and the y-axis shows the smoothed peak density. Profiles are shown separately for regions with increased accessibility in FSHD (Up-DARs, red) and decreased accessibility in FSHD (Down-DARs, teal). (B) Distribution of differentially accessible regions overlapping promoter regions of protein-coding genes. Promoter-associated DARs were categorized based on their distance from the TSS: proximal promoter (≤1 kb), intermediate promoter (1–2 kb), and distal promoter (2–3 kb). Pie charts show the proportion and absolute counts of Up-DARs (total = 467) and Down-DARs (total = 468) in each promoter interval. (C) Volcano plot showing chromatin accessibility changes at promoter regions of protein-coding genes. Each point represents an individual promoter-associated ATAC-seq peak. The x-axis indicates log₂ fold change (FSHD/CTRL), and the y-axis shows −log₁₀(FDR). Up-DARs are shown in red and Down-DARs in teal. Selected genes are labeled. Bar plots on the left and right show selected Gene Ontology (GO) biological process terms associated with genes linked to Down-DARs and Up-DARs, respectively. The x-axis indicates −log₁₀(adjusted P-value). (D) Representative Integrative Genomics Viewer (IGV) screenshot showing an example of a DOWN-DAR overlapping a promoter region of a protein-coding gene. ATAC-seq signal tracks (scale 0-150) from control and FSHD samples are shown aligned to genomic coordinates. (E) Representative IGV screenshot showing an example of a UP-DAR overlapping a promoter region of a protein-coding gene (scale 0-130), displayed as described in panel D. (F) Distribution of peak width for promoter-associated DARs. Violin plots show peak dimension (kb) for Up-DARs and Down-DARs stratified by promoter distance category (proximal, intermediate, distal) and combined categories. Individual data points and median values are shown. Statistical significance is indicated (****). (G) Motif enrichment analysis for transcription factor binding motifs within promoter regions associated with Down-DARs. Each point represents a transcription factor motif. The x-axis shows log₂ odds ratio, and the y-axis shows −log₁₀(q-value). Selected transcription factors are labeled. (H) Motif enrichment analysis for transcription factor binding motifs within promoter regions associated with Up-DARs. Each point represents a transcription factor motif. The x-axis shows log₂ odds ratio, and the y-axis shows −log₁₀(q-value). Selected transcription factors are labeled.

Article Snippet: Primary read processing and downstream ATAC-seq data analysis were performed by Macrogen (Seoul, South Korea).

Techniques: Labeling, Control, Binding Assay

Journal: bioRxiv

Article Title: Stage-dependent chromatin accessibility remodeling defines an architectural state in facioscapulohumeral muscular dystrophy myoblasts

doi: 10.64898/2026.03.06.710110

Figure Lengend Snippet: (A) Percentage of Down-DARs, Up-DARs, all DARs, and all ATAC-seq peaks overlapping nucleolus-associated domains (NADs). Bar plots show the fraction of regions overlapping NADs. Statistical significance was assessed using Fisher’s exact test relative to all ATAC-seq peaks, as indicated. (B) Chromosome-specific enrichment of DARs within nucleolus-associated domains (NADs). Heatmap showing log₂ odds ratio (OR) values for enrichment of Down-DARs and Up-DARs across chromosomes 1–22. Each row represents a chromosome, and columns indicate Down-DARs and Up-DARs. Color intensity corresponds to log₂(OR), and statistical significance is indicated. (C) Percentage of Down-DARs, Up-DARs, all DARs, and all ATAC-seq peaks overlapping lamina-associated domains (LADs). Bar plots show the fraction of regions overlapping LADs. Statistical significance was assessed using Fisher’s exact test relative to all ATAC-seq peaks, as indicated. (D) Chromosome-specific enrichment of DARs within lamina-associated domains (LADs). Heatmap showing log₂ odds ratio values for enrichment of Down-DARs and Up-DARs across chromosomes. Each row corresponds to a chromosome, and columns indicate Down-DARs and Up-DARs. Color intensity represents log₂(OR), and statistical significance is indicated. (E) Compartment enrichment analysis showing log₂ odds ratio values for enrichment of Down-DARs, Up-DARs, and DAR hotspots in NAD and LAD compartments. Values are shown together with corresponding confidence intervals. (F) Chromatin state composition of DARs. Stacked bar plots showing the fraction of Down-DARs and Up-DARs assigned to different chromatin states, including heterochromatin, weak transcription, weak enhancer, transcription elongation, strong enhancer, repressed, transcription transition, insulator, weak promoter, active promoter, poised promoter, and repetitive/CNV. (G) Chromatin state distribution of DARs across chromosomes. Bubble plots showing the percentage of DARs associated with each chromatin state across chromosomes 1–22 and chromosome X. Circle size represents the fraction of DARs, and color indicates log₂ odds ratio for enrichment. Separate panels are shown for Down-DARs and Up-DARs. (H) Enrichment of repeat element classes in Up-DARs. Bar plot showing log₂ odds ratio values for overlap between Up-DARs and annotated repeat classes, including LINE, SINE, DNA elements, simple repeats, and LTR elements. (I) Enrichment of repeat element classes in Down-DARs. Bar plot showing log₂ odds ratio values for overlap between Down-DARs and annotated repeat classes, including LINE, SINE, simple repeats, low complexity regions, and tRNA elements.

Article Snippet: Primary read processing and downstream ATAC-seq data analysis were performed by Macrogen (Seoul, South Korea).

Techniques: