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SRX13669317: GSM5782086: SG_1L1D; Bombyx mori; RNA-Seq
4 ILLUMINA (Illumina NovaSeq 6000) runs: 347.4M spots, 104.2G bases, 36.7Gb downloads

External Id: GSM5782086_r1
Submitted by: State Key Laboratory of Silkworm Genome Biology Southwest University
Study: A single-cell transcriptomic atlas characterizes the silk-producing organ in the silkworm
show Abstracthide Abstract
The silk gland (SG) of the domesticated silkworm Bombyx mori, an economically important insect that has been used for silk production for over 5000 years, is a remarkable organ that produces vast amounts of silk with exceptional properties . Little is known about which SG cells execute silk protein synthesis and its precise spatiotemporal control. Here, we used single-cell RNA-seq to build a comprehensive cell atlas of the B. mori SG, consisting of 14,972 high-quality cells representing 10 distinct cell types, in three early developmental stages. We annotated all 10 cell types and determined their distributions in each region of the SG, decoded their developmental trajectory and gene-switch status, and discovered marker genes involved in the regulation of SG development and silk protein synthesis. Our study reveals the high heterogeneity of B. mori SG cells and their gene expression dynamics for the first time, affording a deeper understanding of silk-producing organs at the single-cell level . Overall design: SG cells collected from B. mori at three developmental stages (8 days post-egg laying, E8D; 1L1D; and first larval molting, 1LM), using single-cell RNAseq
Sample: SG_1L1D
SAMN24744555 • SRS11554953 • All experiments • All runs
Organism: Bombyx mori
Library:
Name: GSM5782086
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Single cells were suspended in calcium- and magnesium-free PBS containing 0.04% weight/volume BSA. Then Cells were added to each channel. After generation of GEMs, reverse transcription reactions were engaged barcoded full-length cDNA followed by the disruption of emulsions using the recovery agent and cDNA clean up with DynaBeads Myone Silane Beads (Thermo Fisher Scientific). Subsequently, the amplified cDNA was fragmented, end-repaired, A-tailed, and index adaptor ligated and library amplification. After the cell viability test, single-cell separation, complementary DNA amplification and library construction were performed according to the manufacturer's protocol for Chromium Single-cell 3' Kits (10× Genomics).
Runs: 4 runs, 347.4M spots, 104.2G bases, 36.7Gb
Run# of Spots# of BasesSizePublished
SRR1749912491,651,24627.5G9.7Gb2022-05-07
SRR17499125109,750,80532.9G11.6Gb2022-05-07
SRR1749912679,126,58623.7G8.3Gb2022-05-07
SRR1749912766,866,58020.1G7.1Gb2022-05-07

ID:
19006206

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