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A role for astrocytic miR-129-5p in Frontotemporal Dementia

GSE262895 Mus musculus (mouse) RNA-seq (gene expression) 32 samples Submitted 2025/04/17 Platform GPL13112
At a glance

RNA-seq (gene expression) · mouse · 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
Mus musculus (mouse)
Samples
32 samples: 7 conditions, mostly with about 5 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 role for astrocytic miR-129-5p in frontotemporal dementiaTranslational psychiatry · 2025
Summary (written by the submitters)
Frontotemporal dementia is a debilitating neurodegenerative disorder characterized by frontal and temporal lobe degeneration, resulting in behavioral changes, language difficulties, and cognitive decline. In this study, smallRNA sequencing was conducted on postmortem brain tissues obtained from FTD patients with GRN, MAPT, or C9ORF mutations, focusing on the frontal and temporal lobes.
Read the full summary ↓
Our analysis identified miR-129-5p as consistently deregulated across all mutation conditions and brain regions. Functional investigations revealed a novel role of miR-129-5p in astrocytes, where its loss led to neuroinflammation and impaired neuronal support functions, including glutamate uptake. Depletion of miR-129-5p in astrocytes resulted in the loss of neuronal spines and altered neuronal network activity. These findings highlight miR-129-5p as a potential therapeutic target in neurodegenerative diseases and also sheds light on the role of astrocytes in Frontotemporal dementia pathogenesis.
Published in
A role for astrocytic miR-129-5p in frontotemporal dementia
Kaurani L, Pradhan R, Schröder S et al. · Translational psychiatry 2025 · PMID 40216778 · doi:10.1038/s41398-025-03338-y
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 GSE262895_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 PRJNA1094590 and SRA study SRP498902. Searching any of these in the dataset finder brings you back here.

Study design
7 conditions, mostly with about 5 replicates each
RNA sequencing from primary neurons_sc-control ×6 RNA sequencing from primary astrocytes_sc-con… ×5 RNA-sequencing from mouse primary cortical ne… ×5 RNA sequencing from primary neurons_anti-miR-… ×5 RNA sequencing from primary astrocytes_anti-m… ×4 RNA-sequencing from mouse primary cortical ne… ×4 RNA sequencing from primary astrocytes anti-m… ×2 RNA sequencing from primary astrocytes sc-con… ×1

Supports a between-group comparison across 31 samples.

How we read this: 7 replicated groups read from 32 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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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.