The functional study of a novel MKRN3 missense mutation associated with familial central precocious puberty

Abstract

AbstractCentral precocious puberty (CPP) refers to a syndrome of early puberty initiation with a characteristic increase in the release of gonadotropin‐releasing hormone (GnRH); therefore, it is also called GnRH‐related precocious puberty. About a quarter of idiopathic central precocious puberty (ICPP) may be familial. Studies suggest that mutations of makorin ring finger protein 3 (MKRN3) can cause familial central precocious puberty (FCPP). In this report, we describe a Chinese female patient carrying a novel MKRN3 variant (c.980G>A/p.Arg327His) and presenting the CPP phenotype. This novel variant attenuated its own ubiquitination, degradation, and inhibition on the transcriptional and translational activity of GNRH1, which was verified through functional tests. We can consider this variant as a loss‐of‐function mutation, which subsides the inhibition of GnRH1‐related signaling and gives rise to GnRH‐related precocious puberty.