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Investigation of the impact of transcription factor SP1,MITF and CREB3L1 in HeLa cells

GSE299965 Homo sapiens (human) RNA-seq (gene expression) 20 samples Submitted 2026/05/13 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 conditions, mostly with about 4 replicates eachGroups 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
A coordinated transcriptional program controls de novo Golgi biogenesisThe EMBO journal · 2026
Summary (written by the submitters)
Our previous studies on golgi biogenesis identified candidate Transcription Factors(TFs) that can support this process. Further bioinformatical ad in-vitro analysis revealed that MITF,SP1 and CREB3L1 emerged as the mayor TFs associated with Golgi biogenesis. In this study, we investigated the impact of the overexpression of these TFs in HeLa cells to determine whether the TFs can influence the transcriptome (and in particular golgi genes)
Published in
A coordinated transcriptional program controls de novo Golgi biogenesis
Forno F, Abete D, Polishchuk EV et al. · The EMBO journal 2026 · PMID 42251155 · doi:10.1038/s44318-026-00828-7
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 GSE299965_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 PRJNA1277727 and SRA study SRP592521. Searching any of these in the dataset finder brings you back here.

Study design
5 conditions, mostly with about 4 replicates each
HeLaCTRL ×4 HeLaMITF ×4 HeLaSP1 ×4 HeLaCREB3L1FL ×4 HeLaCREB3L1CA ×4

Supports a between-group comparison across 20 samples.

How we read this: 5 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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