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SRX2426799: GSM2430247: ps_ops; Polyodon spathula; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 45.3M spots, 3.3G bases, 1.7Gb downloads

Submitted by: NCBI (GEO)
Study: Insights into electrosensory organ development, physiology and evolution from a lateral line organ-enriched transcriptome
show Abstracthide Abstract
The anamniote lateral line system, comprising mechanosensory neuromasts and electrosensory ampullary organs, is a useful model for investigating the developmental and evolutionary diversification of different organs and cell types. Zebrafish neuromast development is increasingly well understood, but neither zebrafish nor Xenopus is electroreceptive and our molecular understanding of ampullary organ development is rudimentary. We have used RNA-seq to generate a lateral line-enriched gene-set from late-larval paddlefish (Polyodon spathula). Validation of a subset reveals expression in developing ampullary organs of transcription factor genes critical for hair cell development, and genes essential for glutamate release at hair cell ribbon synapses, suggesting close developmental, physiological and evolutionary links between non-teleost electroreceptors and hair cells. We identify an ampullary organ-specific proneural transcription factor, and candidates for the voltage-sensing L-type Cav channel and rectifying Kv channel predicted from skate (cartilaginous fish) ampullary organ electrophysiology. Overall, our results illuminate ampullary organ development, physiology and evolution. Overall design: mRNA profiles of pooled opercular and fin tissue (3 biological replicates each), manually dissected from stage 46 larval paddlefish (Polyodon spathula), were generated by deep sequencing using the Illumina HiSeq 2500 platform (multiplex paired-end, 2x100 bp).
Sample: ps_ops
SAMN06146129 • SRS1862759 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Opercular (lateral line organ-enriched) and fin (no lateral line organs) tissues were manually dissected and pooled from different sets of 6-7 specimens each, to form three biological replicates. RNA was extracted using Trizol reagent (Ambion), as per manufacturer's protocol. RNA concentration was assessed using a Nanodrop N1000 spectophotometer and integrity using an Agilent 2100 Bioanalyzer (Cambridge Genomic Services). Only samples with a RNA integrity number (RIN) greater than 9 were used for next-generation sequencing. Libraries were prepared following the standard Illumina RNA Library Prep Kit.
Experiment attributes:
GEO Accession: GSM2430247
Links:
Runs: 1 run, 45.3M spots, 3.3G bases, 1.7Gb
Run# of Spots# of BasesSizePublished
SRR553540345,312,0553.3G1.7Gb2017-05-12

ID:
3524960

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