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SRX13924623: GSM5836873: AMCEA1 snRNA-seq; Mus musculus; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 312.5M spots, 37.2G bases, 10.8Gb downloads

Submitted by: NCBI (GEO)
Study: Cross-Species Single-cell Comparative Analysis of Amygdala
show Abstracthide Abstract
The amygdala or amygdala-like structure in the brain are found in all vertebrates, and plays a critical role for emotional processing. But the cellular architecture of amygdala and how they evolved are still elusive. Here, we generated single-nucleus RNA-sequencing data for more than 200,000 cells in human, macaque, mouse and chicken amygdala. Abundant neuronal cell types derived from different subnuclei of amygdala were identified in all datasets. Cross-species analyses revealed GABAergic neurons and GABAergic neuron-enriched subnuclei of amygdala were well-conserved in cellular composition and marker gene expression, whereas glutamatergic neuron-enriched subnuclei were relatively divergent. Furthermore, we discovered that LAMP5+ interneurons were much more numerous in primates, while DRD2+ GABAergic neurons, LAMP5+ and SATB2+ glutamatergic neurons were predominant in the human central amygdalar nucleus (CEA) and basolateral amygdala complex (BLA), respectively. In addition, we also identified GABAergic neuron-enriched subnuclei of amygdala in the chicken. Altogether, our study highlight extremely cell-type diversity in the amygdala across species and their species-specifc adaptations. Overall design: To transcriptomically characterize cell types of the amygdala in mammals and sauropsids, which have been the most diverse and successful group of land vertebrates, we applied snRNA-seq assays (Chromium v3) and focused on human, macaque, mouse and chicken. Human samples were from postmortem donors with very short postmortem interval (within 6 hours), and macaque, mouse and chicken amygdala were freshly dissected. We profiled a total of 17 specimens, including 3 human amygdala samples, 3 macaque amygdala samples, 2 chicken amygdala homolog samples, 4 mouse amygdala samples, 3 mouse basolateral amygdala complex (BLA; made up of the lateral (LA), basal (BA) and basomedial (BM) nucleus) samples, and 2 mouse central amygdalar nucleus (CEA) samples
Sample: AMCEA1 snRNA-seq
SAMN25276427 • SRS11773180 • All experiments • All runs
Organism: Mus musculus
Library:
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Frozen tumor tissue was homogenized into small cell pellets using a glass tissue grinder in ice-cold EZ buffer and incubated on ice for 5 min. Then nuclei were centrifuged at 500 × g for 5 min at 4 °C. Repeat the wash and centrifuge step again. After that, nuclei were resuspended with PBS, and Debris Removal Solution (MACS) was added to effectively remove cell debris. Isolated nuclei were suspended in Nuclei Suspension Buffer (NSB; consisting of 1× PBS, 0.01% BSA and 0.1% RNase inhibitor. A final nuclei suspension was filtered through a 35-μm cell strainer (Corning, Cat #352235) and used for single-cell libraries preparation. Single nuclei were processed using Chromium Single V3 Chemistry Library Kits (10× Genomics) and according to the manufacturer's instructions.
Experiment attributes:
GEO Accession: GSM5836873
Links:
Runs: 1 run, 312.5M spots, 37.2G bases, 10.8Gb
Run# of Spots# of BasesSizePublished
SRR17762219312,488,19837.2G10.8Gb2022-12-13

ID:
19413985

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