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Series GSE208742 Query DataSets for GSE208742
Status Public on Apr 30, 2024
Title Direct neuronal reprogramming of mouse astrocytes is associated with multiscale epigenome remodeling and requires Yy1
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Genome binding/occupancy profiling by high throughput sequencing
Methylation profiling by high throughput sequencing
Other
Summary Direct neuronal reprogramming is a promising approach to regenerate neurons from local glial cells. However, mechanisms of epigenome remodeling and co-factors facilitating this process are unclear. Here, we combine single-cell multiomics with genome-wide profiling of 3D nuclear architecture and DNA methylation in mouse astrocyte-to-neuron reprogramming mediated by Neurogenin2 (Ngn2) and its phosphorylation-resistant form (PmutNgn2), respectively. We show that Ngn2 drives multilayered chromatin remodelling at dynamic enhancer-gene interaction sites. PmutNgn2 leads to higher reprogramming efficiency and enhances epigenetic remodeling associated with neuronal maturation. However, the differences in binding sites or downstream gene activation cannot fully explain this effect. Instead, we identify Yy1, a transcriptional co-factor, recruited by direct interaction with Ngn2 to its target sites. Upon deletion of Yy1, activation of neuronal enhancers, genes, and ultimately reprogramming are impaired without affecting Ngn2 binding. Thus, our work highlights the key role of interactors of proneural factors in direct neuronal reprogramming.
 
Overall design Single cell multiome (scRNA-seeq + scATAC-seq), bulk ATAC-seq, bulk RNA-seq, ChIP-seq, Cut&Run and Methyl-HiC was performed on primary mouse astrocytes (2 days post induction) transduced with doxycycline-inducible lentiviral constructs expressing either GFP, Ngn2 and PmutNgn2 respectively. Since the constructs also expressed GFP, the astrocytes were FACS sorted based on GFP expression. To profile the effect of Yy1 on direct neuronal reprogramming. scRNA-seq and bulk ATAC-seq was performed on Yy1 KO primary mouse astrocytes (2 days post induction) transduced with a doxycycline-inducible lentiviral construct expressing Ngn2.
 
Contributor(s) Pereira A, Diwakar J, Masserdotti G, Beşkardeş S, Simon T, So Y, Martín-Loarte L, Bergemann F, Vasan L, Schauer T, Danese A, Bocchi R, Colomé-Tatché M, Schuurmans C, Philpott A, Straub T, Bonev B, Götz M
Citation(s) 38956165
Submission date Jul 21, 2022
Last update date Aug 08, 2024
Contact name Boyan Bonev
E-mail(s) boyan.bonev@helmholtz-munich.de
Organization name Helmholtz Zentrum München
Lab Bonev Lab
Street address Ingolstädter Landstr. 1
City Neuherberg
State/province Deutschland
ZIP/Postal code 85764
Country Germany
 
Platforms (3)
GPL18480 Illumina HiSeq 1500 (Mus musculus)
GPL24247 Illumina NovaSeq 6000 (Mus musculus)
GPL32159 NextSeq 1000 (Mus musculus)
Samples (64)
GSM6368705 Multiome_scRNA-seq_Astro
GSM6368706 Multiome_scRNA-seq_GFP
GSM6368707 Multiome_scRNA-seq_Ngn2
Relations
BioProject PRJNA860940
SRA SRP387431

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE208742_GFP_ATAC_peaks.bed.gz 3.3 Mb (ftp)(http) BED
GSE208742_GFP_D2.bw 567.0 Mb (ftp)(http) BW
GSE208742_Ngn2_ATAC_peaks.bed.gz 2.9 Mb (ftp)(http) BED
GSE208742_Ngn2_ChIP_peaks.bed.gz 636.4 Kb (ftp)(http) BED
GSE208742_Ngn2_D2.bw 575.8 Mb (ftp)(http) BW
GSE208742_Ngn2_chip_D2.bw 447.3 Mb (ftp)(http) BW
GSE208742_Pereira_et_al_2022_GEO.xlsx 60.8 Kb (ftp)(http) XLSX
GSE208742_PmutNgn2_ATAC_peaks.bed.gz 3.4 Mb (ftp)(http) BED
GSE208742_PmutNgn2_D2.bw 635.5 Mb (ftp)(http) BW
GSE208742_RAW.tar 26.7 Gb (http)(custom) TAR (of BED, BEDGRAPH, BW, MTX, NARROWPEAK, TAB, TSV, TXT)
GSE208742_Yy1_KO_ATAC_merge.bw 154.9 Mb (ftp)(http) BW
GSE208742_Yy1_KO_ATAC_peaks.bed.gz 1.6 Mb (ftp)(http) BED
GSE208742_Yy1_KO_ATAC_rep1.bw 100.2 Mb (ftp)(http) BW
GSE208742_Yy1_KO_ATAC_rep2.bw 81.9 Mb (ftp)(http) BW
GSE208742_Yy1_KO_Ngn2+_ATAC_merge.bw 218.6 Mb (ftp)(http) BW
GSE208742_Yy1_KO_Ngn2+_ATAC_peaks.bed.gz 2.0 Mb (ftp)(http) BED
GSE208742_Yy1_KO_Ngn2+_ATAC_rep1.bw 170.6 Mb (ftp)(http) BW
GSE208742_Yy1_KO_Ngn2+_ATAC_rep2.bw 79.9 Mb (ftp)(http) BW
GSE208742_Yy1_KO_Ngn2+_barcodes.tsv.gz 20.5 Kb (ftp)(http) TSV
GSE208742_Yy1_KO_Ngn2+_features.tsv.gz 186.8 Kb (ftp)(http) TSV
GSE208742_Yy1_KO_Ngn2+_matrix.mtx.gz 42.6 Mb (ftp)(http) MTX
GSE208742_Yy1_KO_barcodes.tsv.gz 20.2 Kb (ftp)(http) TSV
GSE208742_Yy1_KO_features.tsv.gz 186.8 Kb (ftp)(http) TSV
GSE208742_Yy1_KO_matrix.mtx.gz 51.5 Mb (ftp)(http) MTX
GSE208742_Yy1_WT_ATAC_merge.bw 163.7 Mb (ftp)(http) BW
GSE208742_Yy1_WT_ATAC_peaks.bed.gz 1.8 Mb (ftp)(http) BED
GSE208742_Yy1_WT_ATAC_rep1.bw 132.1 Mb (ftp)(http) BW
GSE208742_Yy1_WT_ATAC_rep2.bw 62.6 Mb (ftp)(http) BW
GSE208742_Yy1_WT_Ngn2+_ATAC_merge.bw 136.2 Mb (ftp)(http) BW
GSE208742_Yy1_WT_Ngn2+_ATAC_peaks.bed.gz 1.9 Mb (ftp)(http) BED
GSE208742_Yy1_WT_Ngn2+_ATAC_rep1.bw 81.3 Mb (ftp)(http) BW
GSE208742_Yy1_WT_Ngn2+_ATAC_rep2.bw 76.9 Mb (ftp)(http) BW
GSE208742_Yy1_WT_Ngn2+_barcodes.tsv.gz 21.9 Kb (ftp)(http) TSV
GSE208742_Yy1_WT_Ngn2+_features.tsv.gz 186.8 Kb (ftp)(http) TSV
GSE208742_Yy1_WT_Ngn2+_matrix.mtx.gz 49.1 Mb (ftp)(http) MTX
GSE208742_Yy1_WT_barcodes.tsv.gz 20.5 Kb (ftp)(http) TSV
GSE208742_Yy1_WT_features.tsv.gz 186.8 Kb (ftp)(http) TSV
GSE208742_Yy1_WT_matrix.mtx.gz 50.2 Mb (ftp)(http) MTX
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