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SRX22894418: GSM7975662: snRNA-seq, D. sechellia central brain (noni supplemented), biol rep4; Drosophila sechellia; RNA-Seq
4 ILLUMINA (Illumina HiSeq 4000) runs: 183.2M spots, 25.5G bases, 11.2Gb downloads

External Id: GSM7975662_r1
Submitted by: Sungkyunkwan University
Study: Comparative single-cell transcriptomic atlases reveal conserved and divergent features of drosophilid central brains
show Abstracthide Abstract
To explore how brains change upon species evolution, we generated the first whole central brain comparative single-cell transcriptomic atlases of three closely-related but ecologically-distinct drosophilids: D. melanogaster, D. simulans and D. sechellia. D. melanogaster and D. simulans are cosmopolitan generalists, while the island endemic D. sechellia exhibits extreme niche specialism on the ripe noni fruit of the Morinda citrifolia shrub. The global cellular composition of central brains is well-conserved in the three Drosophila species, but we predicted a few cell types (perineurial glia, sNPF and Dh44 neurons) with divergent frequencies. Gene expression analysis revealed that distinct cell types within the central brain evolve at different rates and patterns; notably, several glial cell types exhibit the greatest divergence between species. Compared to D. melanogaster, the cellular composition and gene expression patterns of the central brain in D. sechellia displays greater deviation than those of D. simulans, indicating that the distinctive ecological specialization of D. sechellia is reflected in the structure and function of its brain. Gene expression changes in D. sechellia encompass metabolic and ecdysone signaling genes, indicative of adaptations to its novel ecological demands. Additional single-cell transcriptomic analysis on D. sechellia revealed genes and cell types responsive to noni juice supplementation, showing glial cells as key sites for both physiological and genetic adaptation to novel conditions. Our comparative transcriptomic atlases of drosophilid brains will provide an entry point to more broadly study the evolvability of nervous systems across and beyond the Drosophila genus. Overall design: Nuclei of Drosophila central brains were isolated using homogenization and FACS sorting and were analyzed by single-nucleus RNA-sequencing.
Sample: snRNA-seq, D. sechellia central brain (noni supplemented), biol rep4
SAMN38847200 • SRS19866468 • All experiments • All runs
Library:
Name: GSM7975662
Instrument: Illumina HiSeq 4000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC SINGLE CELL
Selection: cDNA
Layout: PAIRED
Construction protocol: Newly-eclosed 30-50 male and female adult flies were collected and placed together for mating, followed by sorting by sex on day 5. The central brains of 20 mated female flies were dissected and collected in 100 μl Schneider's medium, flash-frozen in liquid nitrogen, and stored at -80ºC for nuclear extraction. Sample homogenization, single-nucleus suspension, and nuclear sorting were performed using the standard protocol described in the Fly Cell Atlas (Li et al. 2022) To obtain sequencing data from 10,000 nuclei, 15-20,000 nuclei were collected and loaded onto the Chromium Next GEM Chip (10x Genomics). Sequencing libraries were prepared with the Chromium Single Cell 3ʹ reagent kit v3.1 dual index, strictly following the manufacturer's recommendations.
Runs: 4 runs, 183.2M spots, 25.5G bases, 11.2Gb
Run# of Spots# of BasesSizePublished
SRR2721567445,887,1426.4G2.8Gb2023-12-15
SRR2721567545,826,9846.4G2.8Gb2023-12-15
SRR2721567645,669,2356.3G2.8Gb2023-12-15
SRR2721567745,835,6966.4G2.8Gb2023-12-15

ID:
30954319

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