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SRX5299942: GSM3581496: Harlequin duck Replicate 3; Histrionicus histrionicus; RNA-Seq
14 ILLUMINA (Illumina HiSeq 2500) runs: 52.2M spots, 7.9G bases, 3.9Gb downloads

Submitted by: NCBI (GEO)
Study: RNASeq of trigeminal ganglia of chicken and wild duck species
show Abstracthide Abstract
A major challenge in biology is to link cellular and molecular variations with behavioral phenotypes. Here, we approached this by studying somatosensory neurons from a panel of bird species from the family Anatidae, known for their tactile-based foraging behavior. We found that tactile specialists exhibit a proportional expansion of neuronal mechanoreceptors in trigeminal ganglia. The expansion of mechanoreceptors occurs via neurons with intermediately and slowly inactivating mechano-current. Such neurons contain the Piezo2 ion channel, whose expression positively correlates with the expression of factors responsible for the development and function of touch receptors. Conversely, Piezo2 expression negatively correlates with expression of molecules mediating the detection of temperature and pain, suggesting that the expansion of Piezo2-containing mechanoreceptors with prolonged mechano-current occurs at the expense of other types of sensory neurons. Our study reveals a general mechanism of tactile specialization in vertebrates at the level of somatosensory system. Overall design: High-throughput deep sequencing of the mRNA isolated from trigeminal ganglia of 7 bird species; 3 biological replicates per species; Total of 21 samples.
Sample: Harlequin duck Replicate 3
SAMN10833211 • SRS4298898 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Trigeminal ganglia were dissected from embryos, flash-frozen and stored at -80°C until RNA isolation. Total RNA was isolated from the stored trigeminal ganglia using the TRIzol reagent (ThermoFisher, Waltham, MA) according to manufacturer's instructions. RNA quality and integrity was confirmed by running on Agilent Bioanalyzer, with RINs in the range of 7.7-8.6. mRNA was purified from ~500 ng total RNA with oligo-dT beads. Strand-specific sequencing libraries were prepared using the KAPA mRNA Hyper Prep kit (Roche Sequencing, Pleasanton, CA).
Experiment attributes:
GEO Accession: GSM3581496
Links:
Runs: 14 runs, 52.2M spots, 7.9G bases, 3.9Gb
Run# of Spots# of BasesSizePublished
SRR84957584,000,000608M288.2Mb2019-02-04
SRR84957594,000,000608M299.3Mb2019-02-04
SRR84957604,000,000608M315.6Mb2019-02-04
SRR84957614,000,000608M295.8Mb2019-02-04
SRR84957624,000,000608M312.4Mb2019-02-04
SRR8495763195,23729.7M17.6Mb2019-02-04
SRR84957644,000,000608M307.9Mb2019-02-04
SRR84957654,000,000608M310.2Mb2019-02-04
SRR84957664,000,000608M319.3Mb2019-02-04
SRR84957674,000,000608M313.4Mb2019-02-04
SRR84957684,000,000608M304.1Mb2019-02-04
SRR84957694,000,000608M312.3Mb2019-02-04
SRR84957704,000,000608M291.6Mb2019-02-04
SRR84957714,000,000608M314.9Mb2019-02-04

ID:
7173885

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