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Regulation of eNOS by METTL3 in endothelial cells controls blood pressure via RUNX1b

GSE248592 Homo sapiens (human) RNA-seq (gene expression) 14 samples Submitted 2024/11/01 Platform GPL20795Platform GPL30209
At a glance

RNA-seq (gene expression) · human · 14 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
14 samples: 10 distinct titles, 2 of them repeatedGroups 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
Regulation of blood pressure by METTL3 via RUNX1b-eNOS pathway in endothelial cells in miceCardiovascular research · 2025
Summary (written by the submitters)
As a core subunit of the m6A methyltransferase complex, the downregulation of METTL3 expression in response to Ang II suggests the potential regulation of m6A modification. Our data suggests METTL3 may mediate the dynamic change in m6A landscapes between Ang II with and without overexpression of METTL3.
Published in
Regulation of blood pressure by METTL3 via RUNX1b-eNOS pathway in endothelial cells in mice
Zhang Y, Yang X, Lan M et al. · Cardiovascular research 2025 · PMID 39530587 · doi:10.1093/cvr/cvae242
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 GSE248592_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 PRJNA1044819 and SRA study SRP474054. Searching any of these in the dataset finder brings you back here.

Study design
10 distinct titles, 2 of them repeated
HUVECs, si-NC ×3 HUVECs, si-METTL3 ×3

How we read this: Read from 14 sample titles: 10 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
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