Neuronal activity-driven 3D chromatin dynamics in cortical pyramidal neurons depend on SATB2.
The 8 matches · 5 of them tie a paragraph to a whole file, not to given lines: weak matches, whose lines are not tinted
- [1] § Materials and methods › RNA-seq › RNA-seq analysis ↔ RNAseq/S01_MappingAnalysis.sh, the whole file · a weak match · score 0.77 · featureCOUNTS, STAR, flagstated, subreads, trimmomatic, jar
- [2] § Materials and methods › Hi-C data analysis › Topologically associating domains and TAD cliques ↔ SpectralTAD/runSpectralTAD.R, the whole file · a weak match · score 0.75 · HiCcompare, SpectralTAD, hicpro2bedpe, TADs, chromosome, matrices
- [3] § Materials and methods › Hi-C data analysis › Topologically associating domains and TAD cliques ↔ GENOVA/TAD_N_Analysis.R, the whole file · a weak match · score 0.69 · intra_inter_TAD, interaction density, GENOVA, neighbours, HiC, resolution
- [4] § Materials and methods › ATAC-seq › ATAC-seq analysis ↔ RNAseq/S01_MappingAnalysis.sh, the whole file · a weak match · score 0.68 · DeepTools, R2, SAMtools, dup, R1, BAM
- [5] § Materials and methods › Hi-C data analysis › Mapping, filtering, normalization, and quality control ↔ HiCReproducibility/RunHiCReproducibility.R, lines 30–63 · score 0.59 · HiCRep, reproducibility, lbr, ubr, SCC, resolution
- [6] § Materials and methods › RNA-seq › RNA-seq analysis ↔ RNAseq/S02_Differential_analysis.R, lines 1–44 · score 0.57 · DESeq2, RUVseq, Raw, matrices, genes
- [7] § Materials and methods › Hi-C data analysis › Mapping, filtering, normalization, and quality control ↔ HiCReproducibility/HiCreproducibility.R, lines 11–53 · score 0.55 · get.scc, reproducibility, lbr, ubr, Hi, matrices
- [8] § Results › SATB2 is required for neuronal activity-triggered chromatin compaction ↔ GENOVA/TAD_N_Analysis.R, the whole file · a weak match · score 0.50 · neighbouring TADs, inter TAD, cKO, Bic, interactions
Paper
Loaded from Europe PMC by your browser, not stored by OSCR: doi.org · Europe PMC
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The authors' code
Shell · 42 lines · 1.8 KB · no license · 2 matches
- #!/bin/bash
- ##
- #SBATCH -N 1
- #SBATCH --partition=skylake_0384
- #SBATCH --qos=skylake_0384
- #SBATCH --ntasks-per-node=48
- #SBATCH -J RNAseq
- source activate /SergioEG/tools/DeepTools
- STAR=/tools/STAR-2.7.6a/bin/Linux_x86_64/STAR
- bamCoverage=/tools/deepTools/bin/bamCoverage
- featureCOUNTS=/tools/subread-2.0.1-source/bin/featureCounts
- samtools=/tools/samtools-1.11/samtools
- trimmonatic=/tools/trimmomatic/classes/trimmomatic.jar
- in=/gpfs/data/fs71524/SergioEG/fastq_repository/RNAseq.rescue
- in2=/gpfs/data/fs71524/SergioEG/fastq_repository
- out=/gpfs/data/fs71524/SergioEG/analysis/RNA-seq.Rescue/mouse.rescue
- genomeDir=/resources/genomes/mouse/GRCm38.p6.vM25/STAR
- REF=/resources/genomes/mouse/GRCm38.p6.vM25/GRCm38.p6.genome.fa
- GTF=resources/genomes/mouse/GRCm38.p6.vM25/gencode.vM25.annotation.gtf
- find $in -name \*.fq.gz -printf '%f\n' | awk -F '_E' '{print $1}' | sort | uniq > $in2/filenames.txt
- cd $out/flx_1
- $STAR --runThreadN 48 --genomeDir $genomeDir --sjdbGTFfile $GTF --sjdbOverhang 100 --readFilesIn /fastq_repository/flx_1/flx_1.R1.fastq /fastq_repository/RNAseq.rescue/flx_1.R2.fastq --twopassMode Basic --outSAMtype BAM SortedByCoordinate Unsorted --quantMode TranscriptomeSAM GeneCounts
- $samtools index $out/flx_1/Aligned.sortedByCoord.out.bam
- $samtools flagstat $out/flx_1/Aligned.sortedByCoord.out.bam > $out/flx_1/flx_1.report.txt
- $samtools index $out/flx_1/Aligned.sortedByCoord.bam
- bamCoverage -b $out/flx_1/Aligned.sortedByCoord.bam -o $out/flx_1/flx_1.bw -p max
- mv $out/flx_1/Aligned.sortedByCoord.out.bam $out/flx_1/Aligned.sortedByCoord.bam
- $featureCOUNTS -T 40 --ignoreDup -a $GTF -g gene_name -O -o $out/flx_1/flx_1.exon.gene_name.txt $out/flx_1/Aligned.sortedByCoord.bam
- awk -F"\t" '{print $7}' $out/flx_1/flx_1.exon.gene_name.txt > $out/flx_1/flx_1.exon.gene_name.counts.txt
- awk -F"\t" '{print $1}' $out/flx_1/flx_1.exon.gene_name.txt > $out/features.txt
S01_MappingAnalysis.sh at commit 9ffea7a, no license · at the source
Overview
Abstract
Neuronal activity induces widespread changes in chromatin organization, yet the mechanisms of activity-dependent 3D genome remodelling remain incompletely understood. Here, we identify SATB2 as a key regulator of activity-dependent 3D chromatin dynamics in cortical pyramidal neurons. Using primary cultures from floxed and Satb2 conditional knockout mice, we combined Hi-C and chromatin accessibility mapping to capture rapid 3D epigenome reorganization following neuronal stimulation. Within 1 h of activation, floxed neurons exhibited enhanced chromatin interactions, increased chromatin accessibility, and the emergence of a novel activity-dependent (AD) compartment enriched for SATB2 binding sites. The AD compartment harbours metabolic and housekeeping genes that undergo transient repression upon neuronal activation, thereby prioritizing translation of long synaptic transcripts. Loss of SATB2 disrupted these activity-induced changes, including chromatin accessibility, long-range interactions, and AD compartment formation, resulting in attenuated induction and repression of key activity-regulated genes. These findings establish SATB2 as a central organizer of activity-dependent chromatin architecture dynamics, required for coordinated activation and repression of activity-regulated genes in cortical pyramidal neurons.
Reproduced under the paper's license (CC BY), from the paper cited above.
Repositories
Its files are read in the Code ↔ Paper reader above, with 8 matches between paragraphs and lines of code.
sespesogil/satb2_3d_genome
9ffea7a7eec0e161bf5eb618abdf2f0950886ae5, 24 January 2024Availability: 1 check, the latest on 26 September 2026: the link answers
- 26 September 2026: the link answers
19 files
- Decay_plots/
DecayFreq.R , R, 36 lines - Decay_plots/
importICEDinteractions.R , R, 44 lines - Enriched_permutate/
Enrich_permutateMouse.sh , Shell, 111 lines - Enriched_permutate/
Enriched_permutateHuman. , Shell, 104 linessh - FIREs/
implementation.R , R, 19 lines - FIREs/
renameSparseToDense.sh , Shell, 21 lines - GENOVA/
SaddlePlots.R , R, 44 lines - GENOVA/
TAD_N_Analysis.R , R, 26 lines, 2 matches - HiCReproducibility/
HiCreproducibility.R , R, 54 lines, 1 match - HiCReproducibility/
InputGeneration/ , Shell, 18 linesHicPro2Juicebox.sh - HiCReproducibility/
RunHiCReproducibility.R , R, 63 lines, 1 match - Mustache/
Diff.Chrom.Loops.sh , Shell, 8 lines - Mustache/
mustache.to.FANC.sh , Shell, 45 lines - Mustache/
mustache.to.WashU.sh , Shell, 46 lines - RNAseq/
S01_MappingAnalysis.sh , Shell, 42 lines, 2 matches - RNAseq/
S02_Differential_analysi , R, 489 lines, 1 matchs.R - SpectralTAD/
runSpectralTAD.R , R, 29 lines, 1 match - dcHIC/
annotator/ , R, 10 linesdcHiC.aggregate.R - README.md, Text, 9 lines
ay-lab/dchic
144b4dfed665a8ddbd90ab3bff778736e8fde796, 10 January 2024Availability: 1 check, the latest on 26 September 2026: the link answers
- 26 September 2026: the link answers
10 files
- dchicf.r, R, 2,976 lines
- utility/
Chromosome_ArmWise_PCA/ , Perl, 97 linesrun_dcHiC_chrArms_combin e_step2.pl - utility/
Chromosome_ArmWise_PCA/ , Perl, 211 linesrun_dcHiC_chrArms_pca_st ep1.pl - utility/
getcHiCinputfromExisting , R, 45 linesPCs.r - utility/
mergeDEcompartments.sh , Shell, 10 lines - utility/
pcacluster.r , R, 327 lines - utility/
preprocess.py , Python, 184 lines - utility/
reselectpc.r , R, 79 lines - LICENSE, License, 21 lines
- README.md, Text, 251 lines
Ali-Mujahid/Satb2-3D-Genome-organization
7a0c5d488472589da7095448d3e2ccaeff484858, 17 March 2026Availability: 1 check, the latest on 26 September 2026: the link answers
- 26 September 2026: the link answers
Zenodo 21534635
Availability: 1 check, the latest on 26 September 2026: the link answers (HTTP 200)
- 26 September 2026: the link answers (HTTP 200)
The paper's code and data availability statement is in the Data section.
Tracing map
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- 8 matches between paragraphs of the paper and lines of the code (method lexical-v1);
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Its JSON (tracing-map.json) is deposited on Zenodo with its DOI once the map is validated.
Data
No dataset and no data link were found in the paper.
Data availability
Original data generated in this study have been deposited at GEO and are available as the following GEO records: GSE307197 (CUT&
Reproduced under the paper's license (CC BY), from the paper cited above.
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Version 1, 27 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 5 authors, 10 MeSH terms, 2 funders, 73 references.
Cite
This paper
Wahl, N., Ali, M., Espeso-Gil, S., Dechant, G., & Apostolova, G. (2026). Neuronal activity-driven 3D chromatin dynamics in cortical pyramidal neurons depend on SATB2. Nucleic acids research, 54(16), gkag788. https://
BibTeX
@article{wahl2026neurona
author = {Wahl, Nico and Ali, Mujahid and Espeso-Gil, Sergio and Dechant, Georg and Apostolova, Galina},
title = {{Neuronal activity-driven 3D chromatin dynamics in cortical pyramidal neurons depend on SATB2}},
journal = {Nucleic acids research},
year = {2026},
month = aug,
volume = {54},
number = {16},
pages = {gkag788},
publisher = {Oxford University Press},
issn = {0305-1048},
doi = {10.1093/
url = {https://
pmid = {42639793},
pmcid = {PMC13504278}
}
RIS
TY - JOUR
AU - Wahl, Nico
AU - Ali, Mujahid
AU - Espeso-Gil, Sergio
AU - Dechant, Georg
AU - Apostolova, Galina
TI - Neuronal activity-driven 3D chromatin dynamics in cortical pyramidal neurons depend on SATB2
T2 - Nucleic acids research
J2 - Nucleic Acids Res
PY - 2026
DA - 2026/
VL - 54
IS - 16
SP - gkag788
SN - 0305-1048
PB - Oxford University Press
DO - 10.1093/
UR - https://
LA - en
ER -
CSL-JSON
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