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Series GSE242966 Query DataSets for GSE242966
Status Public on Jul 01, 2024
Title METTL7B is an essential epigenetic regulator of lineage specification in glioblastoma [scRNAseq]
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Glioblastomas are the most common malignant brain tumours in adults; they are highly aggressive, heterogeneous and plastic. We have identified METTL7B as an essential regulator of lineage specification in glioblastoma, with impact on both tumour size and invasiveness in in vivo models. Single cell transcriptomic analysis of these tumours and of cerebral organoids derived from expanded potential stem cells overexpressing METTL7B identified a regulatory role for the gene in the neural stem cells to astrocyte differentiation trajectory. Mechanistically, METTL7B downregulates the expression of key neuronal differentiation players, including SALL2, via DNA methylation and post-translational modifications of histone marks.
 
Overall design 1) scRNAseq of GIC xenografts, with scrambled or anti-METTL7B shRNA 2) scRNAseq of control (PK/PK-Cas9) COs vs METTL7B-OE COs
 
Contributor(s) Marino S, Constantinou M, Nicholson J, Maniati E, Badodi S
Citation(s) 38848215
Submission date Sep 12, 2023
Last update date Jul 02, 2024
Contact name James Nicholson
E-mail(s) james.nicholson@qmul.ac.uk
Organization name Queen Mary University of London
Department Blizard Institute
Street address 4 Newark St
City London
ZIP/Postal code E1 2AT
Country United Kingdom
 
Platforms (1)
GPL24676 Illumina NovaSeq 6000 (Homo sapiens)
Samples (9)
GSM7776158 CO19PK
GSM7776159 CO19M7B
GSM7776160 CO61CAS9PK
This SubSeries is part of SuperSeries:
GSE243132 METTL7B is an essential epigenetic regulator of lineage specification in glioblastoma
Relations
BioProject PRJNA1015630

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Supplementary file Size Download File type/resource
GSE242966_RAW.tar 611.8 Mb (http)(custom) TAR (of MTX, TSV)
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Raw data are available in SRA

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