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SRX9002320: GSM4744936: WT_SG_sample_2; Dictyostelium discoideum; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 75.2M spots, 11.4G bases, 3.1Gb downloads

Submitted by: NCBI (GEO)
Study: RNA-Seq analysis of wild-type and ttpA-C240ins mutant D. discoideum amebae in surface and liquid growth
show Abstracthide Abstract
In many eukaryotes, mRNAs containing specific AU-rich motifs are regulated by proteins of the tristetraprolin (TTP) family, which bind to these motifs through a tandem zinc finger (TZF) domain. This binding leads to promotion of subsequent deadenylation and decay, partly through a conserved carboxyl-terminal CNOT1 binding domain. We explored the physiological role of the single TTP family member (TtpA) expressed in Dictyostelium discoideum. This study shows the effect of an insertional mutation within the TZF domain (ttpA-C240ins), which creates a null genotype, evaluated in amebae in growth medium during surface culture and liquid culture under axenic conditions. The mutant cells exhibited severe growth defects and a multinucleate phenotype during liquid culture, but not in surface culture. Overall design: Dictyostelium discoideum amebae (strain AX3) were grown in normal growth medium under axenic conditions in plastic flasks until they were approximately 80% confluent, or in liquid culture in the same medium until they reached approximately 2 million cells/ml. Six cultures of wild-type cells and six cultures of ttpA-C240ins cells were then frozen and used for RNA extraction and RNA-Seq analysis.
Sample: WT_SG_sample_2
SAMN15897241 • SRS7255278 • All experiments • All runs
Library:
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: RNA was purified using the Illustra RNAspin Kit (GE Healthcare Life Sciences) following the manufacturer's protocol. Total cellular RNA was quantitated with a Qubit fluorometer, and 250 ng of each sample was transcribed to generate cDNA libraries using the Illumina TruSeq RNA Kit (Illumina Inc, San Diego, CA) following the manufacturer's Low Sample (LS) protocol, with the following modifications: 2 minutes of centrifugation were used during the bead drying steps and 12 cycles were used to enrich DNA fragments.
Experiment attributes:
GEO Accession: GSM4744936
Links:
Runs: 1 run, 75.2M spots, 11.4G bases, 3.1Gb
Run# of Spots# of BasesSizePublished
SRR1251166975,184,10111.4G3.1Gb2021-11-25

ID:
11699134

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