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Abstract
The voltage-gated sodium channel Na(V)1.8 (encoded by SCN10A) is predominantly expressed in dorsal root ganglia(DRG) and plays a critical role in pain perception. We analyzed SCN10A transcripts isolated from human DRGs using deep sequencing and found a novel splice variant lacking exon 11, which codes for 98 amino acids of the domain I/II linker. Quantitative PCR analysis revealed an abundance of this variant of up to 5–10% in human, while no such variants were detected in mouse or rat. Since no obvious functional differences between channels with and without the exon-11 sequence were detected, it is suggested that SCN10A exon 11 skipping in humans is a tolerated event.
| Original language | English |
|---|---|
| Journal | Channels |
| Volume | 8 |
| Issue number | 3 |
| Pages (from-to) | 210-5 |
| Number of pages | 6 |
| ISSN | 1933-6950 |
| Publication status | Published - 2014 |
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Dive into the research topics of 'Exon 11 skipping of SCN10A coding for voltage-gated sodium channels in dorsal root ganglia'. Together they form a unique fingerprint.Projects
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Modulation of sensory neuron excitability by functionally altered NaV1.9 channels
Leipold, E. (Principal Investigator (PI))
01.01.14 → 31.12.23
Project: DFG Individual Projects