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SRX19625908: GSM7090737: Dataset D8 lib5; Staphylococcus aureus; RNA-Seq
1 ILLUMINA (NextSeq 500) run: 55.1M spots, 4.6G bases, 1.8Gb downloads

External Id: GSM7090737_r1
Submitted by: NYU Langone Health
Study: A quantitative model for the transcriptional landscape of the bacterial cell cycle
show Abstracthide Abstract
Regulation of gene activity during the cell cycle is fundamental to bacterial replication but is challenging to study in unperturbed, asynchronous bacterial populations. Using single cell RNA-sequencing of heterogeneous Staphylococcus aureus populations, we uncovered a global gene expression pattern dominated by chromosomal position. We show that this pattern results from the effect of DNA replication on gene expression, and in Escherichia coli, changes under different growth rates and modes of replication. By constructing a quantitative model in each species that links replication to cell cycle gene expression, we identified divergent genes that may be instead subject to distinct regulation, and applied this cell cycle framework to characterize heterogeneity in responses to antibiotic stress. Our approach reveals a highly dynamic cell cycle transcriptional landscape and may be broadly applicable across species. Overall design: scRNA-seq by the PETRI-seq method was performed on bacteria of species Escherichia coli and Staphylococcus aureus. scRNA-seq by the PETRI-seq method was performed on bacteria of species Escherichia coli and Bacillus subtilis.
Sample: Dataset D8 lib5
SAMN33706341 • SRS16995783 • All experiments • All runs
Library:
Name: GSM7090737
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC SINGLE CELL
Selection: cDNA
Layout: PAIRED
Construction protocol: Samples were fixed and processed according to the protocol of Blattman et al. (PMID: 32451472). Briefly, cells were fixed overnight with 4% formaldehyde, permeabilized with 50% ethanol followed by enzymatic cell wall digestion (100 µg/ml lysostaphin, 15 min), then treated with DNase to remove genomic DNA. Reverse transcription and split-pool barcode ligation were carried out in situ in fixed cells according to the protocol of Blattman et al. (PMID: 32451472). After barcoding, cells were separated into aliquots of ~20,000 cells for further processing. After lysis and reversal of crosslinking, second strand synthesis was performed using the NebNext Second Strand Synthesis module (New England Biolabs) and tagmentation was carried out using the EZ-Tn5 transposase (Lucigen), before final amplification with multiplex indexing primers.
Runs: 1 run, 55.1M spots, 4.6G bases, 1.8Gb
Run# of Spots# of BasesSizePublished
SRR2379382055,101,8004.6G1.8Gb2023-05-02

ID:
26923654

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