CNTN6基因敲除HEK293细胞

Congenital hypothyroidism (CH) is the most common neonatal metabolic disorder. In patients with CH in China, thyroid dyshormonogenesis is more common than thyroid dysgenesis; however, the genetic causes of CH due to thyroid dyshormonogenesis remain largely unknown. Therefore, we aimed at identifying novel candidate causative genes for CH. To identify novel CH candidate genes, a total of 599 patients with CH were enrolled and next-generation sequencing was performed. The functions of the identified variants were confirmed using HEK293T and FTC-133 cell lines and in a mouse model organism . Three pathogenic contactin 6 () variants were identified in two patients with CH. Pedigree analysis showed that CH caused by variants was inherited in an autosomal recessive pattern. The gene was highly expressed in the thyroid in humans and mice. knockout mice presented with thyroid dyshormonogenesis and CH due to the decreased expression of crucial genes for thyroid hormone biosynthesis (, , and ). All three variants resulted in the blocking of the release of the Notch intracellular domain, which could not translocate into the nucleus, impaired NOTCH1 transcriptional activity, and decreased expression of , , and . Further, we found that DTX1 was required for CNTN6 to promote thyroid hormone biosynthesis through Notch signaling. This study demonstrated that is a novel causative gene for CH through the mediation of thyroid hormone biosynthesis via Notch signaling, which provides new insights into the genetic background and mechanisms involved in CH and thyroid dyshormonogenesis.