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ZBTB48 is a pioneer factor regulating B-cell-specific CIITA expression [RNA-seq]

GSE237958 Homo sapiens (human) RNA-seq (gene expression) 20 samples Submitted 2024/12/26 Platform GPL24676
At a glance

RNA-seq (gene expression) · human · 20 samples

What it is
RNA-seq (gene expression)Gene activity measured by sequencing. The summary does not mention single-cell work, so this is most likely bulk: one average per sample, the usual starting point for comparing groups.
Organism
Homo sapiens (human)
Samples
20 samples: 5 × U2OS cells, WT, RNA-seq vs 5 × U2OS cells, ZBTB48 KO, RNA-seq vs 5 × U2OS cells, WT IFNg, RNA-seq vs 5 × U2OS cells, ZBTB48 KO IFNg, RNA-seqGroups are read from the sample names, not from the paper. Check the list below.
Data you can get
A processed table (series matrix) and supplementary files from NCBI; the raw sequencing reads from ENA. Which of these hold counts depends on the study, so check the file list.
Paper
ZBTB48 is a priming factor regulating B-cell-specific CIITA expressionThe EMBO journal · 2024
Summary (written by the submitters)
CIITA is the master regulator of MHC II gene expression and hence the adaptive immune response. CIITA expression itself is tightly regulated by three cell type-specific promoters, pI, pIII, and by pIV. Here, we demonstrate that the telomere-binding protein and transcriptional activator ZBTB48 directly binds to both the critical activating elements within CIITA pIII and is essential for its gene expression.
Read the full summary ↓
ZBTB48 establishes open chromatin at CIITA pIII upstream of activating H3K4me3 modifications both priming CIITA transcription for IFNg-induction and ensuring constitutive expression in primary murine B cells. Hence, ZBTB48 acts as a molecular on-off-switch for B-cell-specific CIITA expression.
Published in
ZBTB48 is a priming factor regulating B-cell-specific CIITA expression
Rane G, Kuan VLS, Wang S et al. · The EMBO journal 2024 · PMID 39562739 · doi:10.1038/s44318-024-00306-y
This dataset
Download · which file do I need?

Direct links to NCBI and ENA, no account and no request form. Pick by what you want to do: take the small processed table to look, the supplementary files to re-analyse, or the original raw data to start over.

1 · Just have a look

Processed table

The series matrix: one table of values per sample as the submitters processed it. The smallest download, and it opens in Excel or R. Start here to see what the data look like.

2 · Re-analyse it

Supplementary files

The count tables and other files the authors uploaded. Take only the samples you need, or the whole study as GSE237958_RAW.tar (it can run to tens of gigabytes).

3 · Start from the raw reads

Raw sequencing reads

The original FASTQ files, straight from the sequencer, held at ENA. Large, and you align them yourself, so only choose this if you need to re-process the study from scratch.

What the files usually look like: For RNA-seq the counts are usually a table among the supplementary files (look for 'counts', 'expression', 'FPKM' or 'TPM' in the file name). The series matrix of a sequencing study is sometimes nearly empty.

Also filed as BioProject PRJNA997299 and SRA study SRP450804. Searching any of these in the dataset finder brings you back here.

Study design
5 × U2OS cells, WT, RNA-seq vs 5 × U2OS cells, ZBTB48 KO, RNA-seq vs 5 × U2OS cells, WT IFNg, RNA-seq vs 5 × U2OS cells, ZBTB48 KO IFNg, RNA-seq

Supports a between-group comparison across 20 samples.

How we read this: 4 replicated groups read from 20 sample titles; they account for 20 of them. These groups are guessed from the sample names, not taken from the paper, so check them against the sample list below before relying on them.

Samples in this study
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