Mutations in MYO1H cause a recessive form of central hypoventilation with autonomic dysfunction.

Background: Congenital central hypoventilation syndrome (CCHS) is a rare life-threatening disorder of respiratory and autonomic regulation. It is classically caused by dominant mutations in the transcription factor PHOX2B . The objective of the present study was to identify the molecular cause of a recessive form of central hypoventilation with autonomic dysfunction.
Methods: Here, we used homozygosity mapping and whole-genome sequencing in a consanguineous family with CCHS in combination with functional analyses in CRISPR/Cas9 engineered mice.
Results: We report on a consanguineous family with three affected children, all tested PHOX2B mutation negative, presenting with alveolar hypoventilation and symptoms of autonomic dysregulation. Whole-genome sequencing revealed a homozygous frameshift mutation in exon 25 of the MYO1H gene (c.2524_2524delA) segregating with the phenotype in the family. MYO1H encodes for the unconventional myosin IH, which is thought to function as a motor protein in intracellular transport and vesicle trafficking. We show that Myo1h is broadly expressed in the mouse lower medulla, including the CO ₂ -sensitive Phox2b+ retrotrapezoid neurons. To test the pathogenicity of the variant, we engineered two Myo1h mutant mouse strains: the first strain ( Myo1h* ) resembling the human mutation and the second being a full knock-out ( Myo1h ^FS ). Whole-body plethysmography studies in Myo1h* newborns with the re-engineered human mutation revealed hypoventilation and a blunted response to CO ₂ , recapitulating the breathing phenotype observed in the kindred.
Conclusions: Our results identify MYO1H as an important gene in CO ₂ sensitivity and respiratory control and as the cause of a rare recessive form of congenital central hypoventilation.
Competing Interests: Competing interests: None declared.
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