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effect of depletion of Znf143 on gene expression of C2C12 myoblasts with or without induction for myogenic differentiation

GSE314495 Mus musculus (mouse) RNA-seq (gene expression) 12 samples Submitted 2025/12/24 Platform GPL34290
At a glance

RNA-seq (gene expression) · mouse · 12 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
12 samples: 12 samples, each with a distinct title — no replicated groupsGroups 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.
Summary (written by the submitters)
In adults, muscle stem cells (muscle satellite cells, MuSCs) can be recruited to supply myoblasts for routine muscle fibre homeostasis or muscle regeneration. Epigenetic regulation is essential for the proliferation and differentiation of muscle stem cells and myoblasts. We here report that Znf143 is critical for proliferation and differentiation of myoblasts.
Read the full summary ↓
Znf143 depletion in C2C12 myoblasts dramatically repressed their myogenic differentiation, impairing multiple biological processes including striated muscle contraction, muscle cell differentiation, and myofibril assembly. This is consistent with the limited regeneration of skeletal muscle after freeze injury in mice with MuSC-specific Znf143 ablation.
This dataset
Open GSE314495 in finder → Find more mouse RNA-seq datasets →
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.

Series matrix ↓
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 GSE314495_RAW.tar (it can run to tens of gigabytes).

All supplementary files ↗ Whole study · RAW.tar ↓
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.

Raw reads on ENA ↗

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 PRJNA1391407 and SRA study SRP656732. Searching any of these in the dataset finder brings you back here.

NCBI GEO page ↗
Study design
12 samples, each with a distinct title — no replicated groups

Supports a case/control comparison: 3 samples read as cases, 6 as controls.

How we read this: Read from 12 sample titles: 12 distinct titles with little repetition. 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
Datasets on a similar topic

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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.