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SRX18851187: GSM6895327: 7_NT_rep2_24h_S7_LANE1; Homo sapiens; ATAC-seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 57.8M spots, 5.5G bases, 1.8Gb downloads

External Id: GSM6895327_r1
Submitted by: Lahesmaa lab, Turku Bioscience, University of Turku
Study: Chromatin Accessibility Analysis of LIRIL2R-Deficient and LIRIL2R-Sufficient Induced Regulatory T Cells
show Abstracthide Abstract
Factors that determine the epigenetic landscape of regulatory T cells (Tregs), which is critical for their function, remain poorly understood. Long intergenic noncoding RNAs (LincRNA)s are important for shaping and maintaining the epigenetic landscape in different cell types. We identified a novel uncharacterised lincRNA, which we named LincRNA regulator of IL2RA (LIRIL2R), that is upregulated during early differentiation of human Tregs. RNA sequencing (RNA-seq) and data independent (DIA) proteomic analysis of LIRIL2R-deficient Tregs, with genome-wide chromatin occupancy analysis, identified IL2RA as direct LIRIL2R target. This nuclear lincRNA directly binds upstream of IL2RA locus and regulates its transcription by facilitating the accessibility of the locus. LIRIL2R-deficient Tregs had reduced expression of Treg-related genes, including FOXP3, IL2RA, STAT5, CTLA4 and PDCD1, as well as reduced suppressive capacity. Modulating LIRIL2R expression may hold promise for better therapeutic strategies against autoimmunity and cancer. Overall design: CD4 T cells were isolated from human umbilical cord blood. Cells were treated with either contrl non targeting (NT) antisense loked nucleic acid oligos (LNAs) or LNAs targeting LIRIL2R. The cells were differentiated under iTreg conditions for 24/72 hours and ATAC-seq was performed.
Sample: 7_NT_rep2_24h_S7_LANE1
SAMN32409438 • SRS16282462 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: GSM6895327
Instrument: Illumina NovaSeq 6000
Strategy: ATAC-seq
Source: GENOMIC
Selection: other
Layout: PAIRED
Construction protocol: Nuclei were isolated, and the libraries were prepared using Nextera DNA library preparation kit with i7 and i5 indices (15028212). AMPURE-XP beads (B46053, Beckman Coulter) were used to purify the libraries. All samples were pooled into one pool and sequenced on two lanes.
Runs: 1 run, 57.8M spots, 5.5G bases, 1.8Gb
Run# of Spots# of BasesSizePublished
SRR2289346757,755,2315.5G1.8Gb2024-05-15

ID:
25951752

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