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SRX2155843: GSM2308784: Control rep6; Trichechus manatus latirostris; RNA-Seq
1 ILLUMINA (NextSeq 500) run: 35M spots, 9.4G bases, 4.6Gb downloads

Submitted by: NCBI (GEO)
Study: Investigating the Gene Expression Profiles of Florida Manatees (Trichechus manatus latirostris) Rehabilitated Following a Red Tide
show Abstracthide Abstract
To investigate a Florida manatee (Trichechus manatus latirostris) mortality event following a red tide bloom in Southwest Florida, a RNA-Seq experiment was conducted. Cell processes such as immune response, cell proliferation and differentiation and apoptosis were among the most affected by red tide. These were involved in potential diseases such as neoplasms, inflammation, and wounds and injuries, among others. There were both up-regulated and down-regulated genes, but the highest fold changes relative to controls were for genes that were down-regulated. Piccolo presynaptic cytomatrix protein (PCLO) gene, the one most down-regulated (fold change -9.93; p-value 0.0009) is associated with neurotransmitter release, cognitive functioning, neuronal loss, and neuronal synapse function. Another gene that has a similar function, ankyrin 2, neuronal, transcript variant 1 (ANK2) was also down-regulated (fold change -8.66; p-value 0.0023). ANK2 is associated with the stability of neuron synapses. Two immune genes, interleukin 6 (interferon, beta 2) (IL6) and zinc finger protein 804B (ZNF804B), were down-regulated (fold change -9.31; p-value 0.000003 and fold change -8.90; p-value 0.0164, respectively). Interleukin 6 encodes proteins involved in acute phase response, inflammation, and autoimmune response. ZNF804B is associated with neuronal chemokine and cytokine regulation, autoimmune response, and immune activation. The family with sequence similarity 186, member A (FAM186A) gene was down-regulated (fold change -8.79; p-value 0.0143). FAM186A gene mutation is associated with tumor metastasis in colorectal cancer tumors. Among the most up-regulated genes, CCAAT/enhancer binding protein (C/EBP) is involved in granulocytic differentiation and also involved with the immune system. Determining the differentially expressed genes associated with red tide enhances our understanding of manatee immune response to red tide toxins and aids in the development of red tide biomarkers. This information will better assist clinicians and researchers in diagnosing and treating future illnesses. Overall design: White blood cell or 'buffy coat' samples were collected from manatees (n=4) rescued from a red tide affected area and transported to the Lowry Park Zoo in Tampa, FL for rehabilitation. A RNA-Seq experiment was conducted to identify differentially expressed genes in the red tide group compared to a control population of manatees (n=7) from Brevard County (Indian River Lagoon) and Crystal River, FL.
Sample: Control rep6
SAMN05761507 • SRS1685848 • All experiments • All runs
Library:
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Sample preparation included RNA extraction from buffy coats, purification using DNase and column treatments to remove residual DNA contamination, depletion of rRNA and globin using EpiCentre ScriptSeq™ kits, and creation of cDNA libraries following standard protocols (EpiCentre, Madison, WI, USA). RNAlater (Life Technologies™, Carlsbad, CA, USA) was used to preserve the buffy coat samples in a ratio of 1.2 mL RNAlater to <0.5 mL buffy coat according to the manufacturer’s protocol (Life Technologies™). The samples were stored at -20 °C in RNAlater for approximately 9 months. RNA was extracted from manatee buffy coat samples according to the Tel-Test Inc. method for total RNA extraction using Stat-60 in a 1:10 ratio of buffy coat sample to Stat-60 (Tel-Test, Inc., Friendswood, TX) For RNA processing and sequencing library preparation, the Illumina® EpiCentre ScriptSeq™ Complete Gold (Blood)-Low Input Kit (Illumina® EpiCentre, Madison, WI, USA) was used along with the Illumina® FailSafe™ PCR Enzyme Mix and ScriptSeq™ Index PCR primers (set 1). The kit protocols were followed with minor modifications. This kit’s ‘Globin and Ribo-Zero’ reagents were designed to remove globin and rRNA from RNA samples (EpiCentre ScriptSeq™, Madison, WI). The Zymo Research (Irvine, CA, USA) RNA Clean and Concentrator-5 was used to purify RNAs (>200 nt) and concentrate the depleted samples. Individual libraries were made for each of the samples.
Experiment attributes:
GEO Accession: GSM2308784
Links:
Runs: 1 run, 35M spots, 9.4G bases, 4.6Gb
Run# of Spots# of BasesSizePublished
SRR422854634,966,9399.4G4.6Gb2017-10-11

ID:
3150623

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