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Status |
Public on Jan 23, 2021 |
Title |
HN37A - replicate 1 |
Sample type |
SRA |
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Source name |
Yeast cells
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Organism |
Cryptococcus neoformans |
Characteristics |
strain: H99 cell type: Yeast cells protocol: High nitrogen, 37°C
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Growth protocol |
Ammonium chloride (NH4Cl) was used as a nitrogen source in all experimentation and was supplemented as follows: 0.53 g/L NH4Cl for a higher nitrogen concentration (HN) and 0.21 g/L NH4Cl for a lower nitrogen concentration (LN). These nitrogen concentrations were selected based on the lowest ammonium-nitrogen (NH4-N) concentration (ca. 0.16 g NH4-N/kg) of the woody debris from which pathogenic cryptococci were previously isolated. C. neoformans cells were inoculated into 100 mL yeast carbon base (contained in 1L conical flasks) supplemented with HN or LN at a final concentration of 1×106 cells/mL. Following agitated incubation for either 38 h or 28 h at 30°C or 37°C, respectively, total RNA was extracted.
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Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted using an Ambion RiboPureTM-Yeast kit (Thermo Fisher Scientific) according to the manufacturer’s instructions. Four biological repeats were performed for each culture condition. RNA libraries were prepared for sequencing using standard protocols for Ion Torrent sequencing
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Ion Torrent S5 |
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Data processing |
Torrent Suite Version 5.12.0 Software used for basecalling Data were quality filtered (Q>20) using FastX-Toolkit (http://hannonlab.cshl.edu/fastx_toolkit/), and length-filtered (<10 bp) using the awk command (Yalamanchili, Wan and Lui 2017) Read quality assessed with FastQC, whereafter reads were aligned to the reference genome of C. neoformans H99 (Janbon et al. 2014) using HISAT2 v2.1.0 (Kim, Langmead and Salzberg 2015) Alignment quality assessed using Qualimap2 v2.2.1 (Okonechnikov, Conesa and García-Alcalde 2016) and transcript assembly performed using StringTie v1.3.3b (Pertea et al. 2015) Differential gene expression analysis was performed using DeSeq2 v1.20.0 (Love, Huber and Anders 2014) Genome_build: C. neoformans H99 Supplementary_files_format_and_content: Matrix table with raw gene counts for every gene and every sample
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Submission date |
Jan 22, 2021 |
Last update date |
Jan 23, 2021 |
Contact name |
Caylin Bosch |
E-mail(s) |
18344666@sun.ac.za
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Organization name |
Stellenbosch University
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Department |
Microbiology
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Street address |
JC Smuts Building, Van der Byl road
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City |
Stellenbosch |
State/province |
Western Cape |
ZIP/Postal code |
7600 |
Country |
South Africa |
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Platform ID |
GPL29638 |
Series (1) |
GSE165294 |
Transcriptomic response of Cryptococcus neoformans to ecologically relevant nitrogen concentrations |
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Relations |
BioSample |
SAMN17492765 |
SRA |
SRX9916937 |
Supplementary data files not provided |
SRA Run Selector |
Raw data are available in SRA |
Processed data are available on Series record |
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