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SRX24879588: GSM8322901: WTN3DPI,1,S5; Mus musculus; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 868.2M spots, 154.5G bases, 48.7Gb downloads

External Id: GSM8322901_r1
Submitted by: Washington University in St.Louis
Study: snRNAseq analysis of mouse placenta during ZIKV infection
show Abstracthide Abstract
The aim of this study was to study placental immune responses to ZIKV infection at the cell level. WT or MAVS-deficient placentas from mock- or ZIKV- infected pregnant WT or mutant mice were collected, and placentas from male fetuses selected to facilitate the identification of maternal and fetal clusters, and doublets. Two placentas from the same genotype and condition were pooled and processed for isolation of nuclei. Approximately 10,000 nuclei per sample were subjected to gel bead-in-emulsion (GEM) generation, reverse transcription, and construction of libraries for sequencing according to the protocol provided in the 3' gene expression v3.1 kit manual (10X Genomics). We obtained 98,661 nuclei with a median of 3,077 genes detected per nucleus after data processing and quality control. Seurat integrated analysis and graph-based clustering identified cell types in maternal and fetal compartments based on analysis of canonical cellular markers. We performed differential expression test using Wilcoxon test from Seurat to identify the changes in expression across conditions. The DSGs were then used to align to the Hallmark mouse pathway database Msigdbr (Version 7.5.1) with package fgsea (Version 1.26.0) and pathways that with P-adjusted value < 0.05 were chosen as the significantly enriched pathways. We found cell-type specific antiviral pathways driven by MAVS, and MAVS-independent induction of interferon-stimulated and antiviral genes in other cell types. Overall design: Nuclei were obtained from placentas belonging to male WT or MAVS-/- fetuses from mock- or ZIKV-infected mouse fetuses at different gestational stages
Sample: WTN3DPI,1,S5
SAMN41791640 • SRS21588435 • All experiments • All runs
Organism: Mus musculus
Library:
Name: GSM8322901
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC SINGLE CELL
Selection: cDNA
Layout: PAIRED
Construction protocol: Two placentas from the same genotype and condition were pooled and processed for isolation of nuclei. Nuclear extraction was adapted from a previously described protocol for jejunal segments (Chang et al., 2024). Briefly, tissues were thawed and minced in lysis buffer (25 mM citric acid, 250 mM sucrose, 0.1% NP-40, and 1X protease inhibitor (Roche)). Nuclei were released from cells using a Dounce homogenizer (Wheaton) then washed 3 times with buffer (25 mM citric acid, 0.25 M sucrose, 1X protease inhibitor (Roche)), and then filtered successively through 100 μm, 70 μm, and 40 μm diameter strainers (pluriSelect) to obtain single nuclei in resuspension buffer (25 mM KCl, 3 mM MgCl2, 50 mM Tris, 1 mM DTT, 0.4 U/μL RNase inhibitor (Sigma) and 0.4 U/μL Superase inhibitor (ThermoFisher)). Approximately 10,000 nuclei per sample were subjected to gel bead-in-emulsion (GEM) generation, reverse transcription, and construction of libraries for sequencing according to the protocol provided in the 3' gene expression v3.1 kit manual (10X Genomics). Briefly, cDNA was prepared after GEM generation and barcoding, followed by the GEM-RT reaction and bead cleanup steps. Purified cDNA was amplified for 11-13 cycles before clean-up using SPRI select beads (Beckman Coulter, B23318). Samples were then run on a Bioanalyzer to determine cDNA concentrations. Gene expression libraries (GEX libraries) were prepared as recommended by the 10x Genomics Chromium Single Cell 3' Reagent Kits User Guide (v3.1 Chemistry Dual Index) with appropriate modifications to the PCR cycles based on the calculated cDNA concentration. For sample preparation on the 10x Genomics platform, the Chromium Next GEM Single Cell 3' Kit v3.1, 16 rxns (PN-1000268), Chromium Next GEM Chip G Single Cell Kit, 48 rxns (PN-1000120), and Dual Index Kit TT Set A, 96 rxns (PN-1000215) were used. The concentration of each library was determined through qPCR utilizing the KAPA library Quantification Kit according to the manufacturer's protocol (KAPA Biosystems/Roche) to produce cluster counts appropriate for the Illumina NovaSeq6000 instrument. Normalized libraries were sequenced on a NovaSeq6000 S4 Flow Cell using the XP workflow and a 50x10x16x150 sequencing recipe according to manufacturer protocol. A median sequencing depth of 50,000 reads/cell was targeted for each Gene Expression Library.
Runs: 1 run, 868.2M spots, 154.5G bases, 48.7Gb
Run# of Spots# of BasesSizePublished
SRR29365149868,179,036154.5G48.7Gb2024-06-15

ID:
33214222

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