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Degron models: a toolbox for rapid in vivo depletion of essential proteins regulating mRNA metabolism

GSE309776 Mus musculus (mouse) RNA-seq (gene expression) 60 samples Submitted 2026/02/23 Platform GPL24973
At a glance

RNA-seq (gene expression) · mouse · 60 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
60 samples: 21 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
Degron models: a toolbox for rapid in vivo depletion of essential proteins regulating mRNA metabolismCommunications biology · 2026
Summary (written by the submitters)
Due to their essentiality, studying proteins involved in fundamental processes in vivo is challenging. PROTAC-based systems offer time-controlled protein depletion, but their characterization in vivo remains limited. Here, with an efficient direct zygote editing protocol, we generated degron-tag models (dTAG/FKBP or BromoTag) for seven genes involved in therapeutic and endogenous mRNA metabolism (Cnot1, Pan2, Tent5a, Tent4b, Dcp2, Rnasel, Tsg101).
Read the full summary ↓
Degron tags occasionally caused phenotypes that were often mitigated by tag position or tagging system change. In cells, both approaches yielded rapid and sustained degradation. In mice, dTAG depletion was effective but varied by protein and administration route, whereas BromoTag showed no in vivo activity. We showcase the utility of these models through an analysis of CNOT1's roles in cell division, immunity, and poly(A) tail maintenance. We present a valuable toolbox for studying mRNA metabolism in mammalian models, while providing a benchmark for applying degron-tag models to study other biological processes.
Published in
Degron models: a toolbox for rapid in vivo depletion of essential proteins regulating mRNA metabolism
Antczak W, Szpila M, Sałas K et al. · Communications biology 2026 · PMID 41851445 · doi:10.1038/s42003-026-09828-z
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 GSE309776_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 PRJNA1363157 and SRA study SRP644318. Searching any of these in the dataset finder brings you back here.

Study design
21 conditions, mostly in triplicate
liver, CNOT1, dTAG 2h, ×3 liver, CNOT1, dTAG 24h, ×3 liver, CNOT1, DMSO, ×3 liver, WT, dTAG 24h, ×3 BMDM, CNOT1, DMSO, ×3 BMDM, CNOT1, dTAG, ×3 BMDM, DCP2, DMSO, ×3 BMDM, DCP2, dTAG, ×3 +13 more

Supports a between-group comparison across 60 samples.

How we read this: 21 replicated groups read from 60 sample titles; they account for 60 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

+ 20 more — browse all 60 samples with per-sample file links →

Datasets on a similar topic

Search all mouse RNA-seq datasets in GEO →

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Metadata from NCBI GEO, cached and refreshed periodically — the NCBI page above is authoritative. Downloads link straight to NCBI/ENA; nothing is proxied through BioTransfer.