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Open chromatin, HIF binding and mRNA expression analysis in primary tubule and ccRCC cells [RNA-seq]

GSE256000 Homo sapiens (human) RNA-seq (gene expression) 32 samples Submitted 2025/12/15 Platform GPL34284Platform GPL24676
At a glance

RNA-seq (gene expression) · human · 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
Homo sapiens (human)
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
HIF sustain a transcriptional regulatory circuit of EPAS1 expression in renal clear cell carcinomaNature communications · 2026
Summary (written by the submitters)
Inactivation of the von Hippel-Lindau tumor suppressor leads to stabilization of HIF transcription factors and subsequent oncogenic HIF-2 signaling in ccRCC. However, little is known about the transcriptional mechanisms leading to dysregulation of HIF-2α mRNA in renal cancer. Epigenetic analysis of the EPAS1 locus (coding for HIF-2α) using ATAC-seq, ChIP-seq and RNA-seq revealed an oncogenic enhancer that maintains a HIF-dependent feed-forward circuit of HIF-2α regulation in renal tumor cells.
Published in
HIF sustain a transcriptional regulatory circuit of EPAS1 expression in renal clear cell carcinoma
Naas S, Krüger R, Grampp S et al. · Nature communications 2026 · PMID 41714613 · doi:10.1038/s41467-026-68576-0
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 GSE256000_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 PRJNA1077373 and SRA study SRP490101. Searching any of these in the dataset finder brings you back here.

Study design
16 conditions, mostly in duplicate
RNA_PTC_ctrl_1 ×2 RNA_PTC_ctrl_2 ×2 RNA_PTC_ctrl_3 ×2 RNA_ccRCC_ctrl_1 ×2 RNA_ccRCC_ctrl_2 ×2 RNA_ccRCC_ctrl_3 ×2 RNA_760_pool_nt ×2 RNA_760_pool_E2_ko ×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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