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Pre-division TCF1 downregulation determines long-term effector and memory CD8 T cell fates [RNA-Seq]

GSE306744 Mus musculus (mouse) RNA-seq (gene expression) 31 samples Submitted 2026/04/10 Platform GPL24247
At a glance

RNA-seq (gene expression) · mouse · 31 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
31 samples: 9 conditions, mostly in triplicateGroups 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
Pre-division TCF1 drop determines long-term CD8 T cell fatesbioRxiv : the preprint server for biology · 2025
Summary (written by the submitters)
RNA-SEQ analysis of antigen-specific CD8 T cells sorted from the spleens of Listeria-infected mice at different early timepoints following activation. As a control, we sequenced naive CD8 T cells prior to transfer into infected hosts.
Published in
Pre-division TCF1 drop determines long-term CD8 T cell fates
Favret NR, Astorkia M, Wolf MM et al. · bioRxiv : the preprint server for biology 2025 · PMID 41279579 · doi:10.1101/2025.10.06.680655
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 GSE306744_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 PRJNA1312020 and SRA study SRP613932. Searching any of these in the dataset finder brings you back here.

Study design
9 conditions, mostly in triplicate
CD8+CD90.1+CD69+CFSE+ transgenic TCRTAG CD8 T… ×4 CD8+CD90.1+P1-3 transgenic TCRTAG CD8 T cells… ×4 CD8+CD90.1+KLRG1+CD62L- transgenic TCRTAG CD8… ×4 CD8+CD90.1+KLRG1-CD62L+ transgenic TCRTAG CD8… ×4 CD8+CD90.1+CD44low transgenic TCRTAG CD8 T ce… ×3 CD8+CD90.1+P4-6CD25low transgenic TCRTAG CD8 … ×3 CD8+CD90.1+P4-6CD25high transgenic TCRTAG CD8… ×3 CD8+CD90.1+CD44+CD62L+ transgenic TCRTAG CD8 … ×3 +1 more

Supports a between-group comparison across 31 samples.

How we read this: 9 replicated groups read from 31 sample titles; they account for 31 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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