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CTCF tunes gene expression in a loop-dependent and -independent manner [RNA-seq]

GSE274773 Mus musculus (mouse) RNA-seq (gene expression) 32 samples Submitted 2026/05/06 Platform GPL24247
At a glance

RNA-seq (gene expression) · mouse · 32 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
Mus musculus (mouse)
Samples
32 samples: 16 conditions, mostly in duplicateGroups 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
CTCF's loop-independent functions prevail over chromatin looping in the acute degradation systemProtein & cell · 2026
Summary (written by the submitters)
In this study, we aimed to investigate changes in gene expression following CTCF degradation, and found that CTCF primarily regulated gene expression in a loop-independent manner when it bound at gene promoters.
Published in
CTCF's loop-independent functions prevail over chromatin looping in the acute degradation system
Hu G, Ji B, Zhang J et al. · Protein & cell 2026 · PMID 41191909 · doi:10.1093/procel/pwaf087
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 GSE274773_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 PRJNA1147848 and SRA study SRP526227. Searching any of these in the dataset finder brings you back here.

Study design
16 conditions, mostly in duplicate
CTCF_AID_0h ×2 CTCF_AID_12h ×2 CTCF_AID_24h ×2 RAD21_AID_0h ×2 RAD21_AID_12h ×2 RAD21_AID_24h ×2 oectrl ×2 oectrl_IAA ×2 +8 more

Supports a between-group comparison across 32 samples.

How we read this: 16 replicated groups read from 32 sample titles; they account for 32 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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