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Series GSE239759 Query DataSets for GSE239759
Status Public on Feb 19, 2024
Title Cell-type-specific expression of tRNAs in the brain regulates cellular homeostasis
Organism Mus musculus
Experiment type Other
Summary Defects in tRNA biogenesis are associated with multiple neurological disorders, yet our understanding of these diseases has been hampered an inability to determine tRNA expression in individual cell types within a complex tissue. Here, we developed a mouse model in which RNA Polymerase III is conditionally epitope-tagged in a Cre-dependent manner, allowing us to accurately profile tRNA expression in any cell type in vivo. We investigated tRNA expression in eleven diverse nervous system cell types, revealing dramatic heterogeneity in the expression of tRNA genes between populations. We found that while maintenance of levels of tRNA anticodon pools is critical for cellular homeostasis, neurons are differentially vulnerable to insults to distinct tRNA anticodon families. Cell type-specific translatome analysis suggests that the balance between tRNA availability and codon demand may underlie such differential resilience. Our work provides a platform for investigating the complexities of mRNA translation and tRNA biology in the brain.
 
Overall design The RiboTag mouse line (B6N.129-Rpl22tm1.1Psam/J mice) was crossed to appropriate Cre driver lines to obtain Rpl22 Fl/+, CRE + mice, expressing HA-tagged Rpl22 in the appropriate cell populations. The following populations were profiled: Cerebellar granule cells (Gabra6-cre, cerebellum), layer V cortical neurons (Rbp4-cre, cortex), dentate gyrus granule cells (Rbp4-cre, hippocamus), inhibitory interneurons (Dlx6a-cre, hippocampus), astrocytes (Aldh1-cre, cortex), and microglia (Tmem119-cre, cortex). HA-tagged RPL22 and associated mRNAs were immunoprecipitated using Pierce anti-HA magnetic beads (ThermoFisher Scientific) from the appropriate brain regions of 6-week-old mice, and mRNA libraries were made using the Kapa Stranded mRNA-Seq Kit (Roche) according to the manufacturer’s protocol.The design includes three biological replicates for each cell type. For cerebellar granule cells, astrocytes, layer V cortical neurons, and dentate gyrus granule cells, one sample each was sequenced twice to account for batch effects.
Web link https://www.cell.com/neuron/fulltext/S0896-6273(24)00054-0
 
Contributor(s) Kapur M, Ackerman SL
Citation(s) 38377989
Submission date Aug 01, 2023
Last update date Feb 21, 2024
Contact name Mridu Kapur
E-mail(s) mkapur@health.ucsd.edu
Organization name University of California San Diego
Department Cellular and Molecular Medicine
Lab Susan Ackerman
Street address 9500 Gilman Drive
City La Jolla
State/province CA
ZIP/Postal code 92093
Country USA
 
Platforms (1)
GPL24247 Illumina NovaSeq 6000 (Mus musculus)
Samples (22)
GSM7671071 Dentate gyrus granule cells, replicate 1, batch 1
GSM7671072 Dentate gyrus granule cells, replicate 2, batch 1
GSM7671073 Dentate gyrus granule cells, replicate 3, batch 1
Relations
BioProject PRJNA1000925

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Supplementary file Size Download File type/resource
GSE239759_RAW.tar 98.8 Mb (http)(custom) TAR (of TSV)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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