Description:
<jats:p>Mitochondria are fundamental for life and require balanced ion exchange to maintain proper functioning. The mitochondrial cation exchanger LETM1 sparks interest because of its pathophysiological role in seizures in the Wolf Hirschhorn Syndrome (WHS). Despite observation of sleep disorganization in epileptic WHS patients, and growing studies linking mitochondria and epilepsy to circadian rhythms, LETM1 has not been studied from the chronobiological perspective. Here we established a viable <jats:italic>letm1</jats:italic> knock-out, using the diurnal vertebrate <jats:italic>Danio rerio</jats:italic> to study the metabolic and chronobiological consequences of <jats:italic>letm1</jats:italic> deficiency. We report diurnal rhythms of Letm1 protein levels in wild-type fish. We show that mitochondrial nucleotide metabolism is deregulated in <jats:italic>letm1−/−</jats:italic> mutant fish, the rate-limiting enzyme of NAD<jats:sup>+</jats:sup> production is up-regulated, while NAD<jats:sup>+</jats:sup> and NADH pools are reduced. These changes were associated with increased expression amplitude of circadian core clock genes in <jats:italic>letm1−/−</jats:italic> compared with wild-type under light/dark conditions, suggesting decreased NAD(H) levels as a possible mechanism for circadian system perturbation in Letm1 deficiency. Replenishing NAD pool may ameliorate WHS-associated sleep and neurological disorders.</jats:p>