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SRX26116231: GSM8522773: Mouse, female sample1, sublibrary1; Mus musculus; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 443.4M spots, 133G bases, 49Gb downloads

External Id: GSM8522773_r1
Submitted by: Washington University in St. Louis
Study: Transcriptomic landscape of mammalian ventral pallidum at single-cell resolution
show Abstracthide Abstract
The ventral pallidum (VP) is critical for motivated behaviors. While contemporary work has begun to elucidate the functional diversity of VP neurons, the molecular heterogeneity underlying this functional diversity remains incompletely understood. We used snRNA-seq and in situ hybridization to define the transcriptional taxonomy of VP cell types in mice, macaques, and baboons. We found transcriptional conservation between all three species, within the broader neurochemical cell types. Unique dopaminoceptive and cholinergic subclusters were identified and conserved across both primate species but had no homolog in mice. This harmonized consensus VP cellular atlas will pave the way for understanding the structure and function of the VP and identified key neuropeptides, neurotransmitters, and neuro receptors that could be targeted within specific VP cell types for functional investigations. Overall design: VP tissues were dissected from C57Bl6J mice, olive baboons, and rhesus macaque. Nuclear suspension was isolated by FACS based on 7-AAD signal and processed by 10X Genomics.
Sample: Mouse, female sample1, sublibrary1
SAMN43813518 • SRS22679679 • All experiments • All runs
Organism: Mus musculus
Library:
Name: GSM8522773
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Nuclear extraction for both mice and primates was performed with density gradient centrifugation according to the protocol described previously with modifications to scale down the reaction volume (85). Samples were moved from -80 ̊C and thawed on ice for 2 minutes. Tissues were transferred to a dounce homogenizer (Millipore Sigma, D8938-1SET) in homogenization buffer (0.25 M sucrose, 25 mM KCl, 5 mM MgCl2, 10 mM Tris-HCl, pH 8.0, 5 µg/mL actinomycin, 1% BSA, and 0.08 U/µl RNase inhibitor, 0.01% NP40) on ice. Samples were homogenized for 10 strokes with the loose pestle in a total volume of 1 mL, followed by 10 additional strokes with the tight pestle. The tissue homogenate was then passed through a 50 µm filter and diluted 1:1 with working solution (50% iodixanol, 25 mM KCl, 5 mM MgCl2, and 10 mM Tris-HCl, pH 8.0). Nuclei were layered onto an iodixanol gradient after homogenization and ultracentrifuged as described previously. After ultracentrifugation, nuclei were collected between the 30 and 40% iodixanol layers and diluted with resuspension buffer (1xPBS with 1% BSA, and 0.08 U/µl RNase inhibitor). Nuclei were centrifuged at 500 g for 10 min at 4°C and resuspended in resuspension buffer with 5 ng/µl of 7-AAD. FACS was carried out to further remove cellular debris. 7-AAD+ events were collected using a 100 µm nozzle on a BD FACSAria III instrument into a 1.5 mL microcentrifuge tube. Nuclei were processed according to the manufacturer's manual of 10X Genomics Chromium Single Cell Gene Expression 3' V3.1 Assay.
Runs: 1 run, 443.4M spots, 133G bases, 49Gb
Run# of Spots# of BasesSizePublished
SRR30712462443,379,417133G49Gb2024-10-31

ID:
35235181

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