A Novel Na+ Channel Splice Form Contributes to the Regulation of an Androgen-Dependent Social Signal

Na+ channels are often spliced but little is known about the functional consequences of splicing. We have been studying the regulation of Na+ current inactivation in an electric fish model in which systematic variation in the rate of inactivation of the electric organ Na+ current shapes the electric organ discharge (EOD), a sexually dimorphic, androgen-sensitive communication signal. Here, we examine the relationship between an Na+ channel (Nav1.4b), which has two splice forms, and the waveform of the EOD. One splice form (Nav1.4bL) possesses a novel first exon that encodes a 51 aa N-terminal extension. This is the first report of an Na+ channel with alternative splicing in the N terminal. This N terminal is present in zebrafish suggesting its general importance in regulating Na+ currents in teleosts. The extended N terminal significantly speeds fast inactivation, shifts steady-state inactivation, and dramatically enhances recovery from inactivation, essentially fulfilling the functions of a β subunit. Both splice forms are equally expressed in muscle in electric fish and zebrafish but Nav1.4bL is the dominant form in the electric organ implying electric organ-specific transcriptional regulation. Transcript abundance of Nav1.4bL in the electric organ is positively correlated with EOD frequency and lowered by androgens. Thus, shaping of the EOD waveform involves the androgenic regulation of a rapidly inactivating splice form of an Na+ channel. Our results emphasize the role of splicing in the regulation of a vertebrate Na+ channel and its contribution to a known behavior.

• Publication year

  2008

• Venue

  Journal of Neuroscience

• Publication date

  2008-09-10

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1523/JNEUROSCI.2783-08.2008PMID 18784298PMCID PMC2615813
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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