Identification and characterization of human NR4A2 polymorphisms in attention deficit hyperactivity disorder

Abstract Attention deficit hyperactivity disorder (ADHD) is a highly heritable and common disorder thought to arise, in part, from alterations in dopamine function. NR4A2, or Nurr1, is an orphan nuclear receptor implicated in the development of dopaminergic cells of the ventral tegmental area (VTA) and the substantia nigra (SN). Dopaminergic cells of the VTA provide innervation to the prefrontal cortex, believed to be of major importance in the etiology of ADHD, suggesting that NR4A2 is a potential candidate gene for ADHD susceptibility. This study aimed to identify polymorphisms in NR4A2 and test their association to ADHD. Database analysis revealed a CA repeat polymorphism in the 3′ UTR of NR4A2 that was confirmed by PCR. SSCP screening revealed a common ΔC polymorphism, 254 bp 5′ to the transcriptional start site. These polymorphisms were tested for an association with ADHD in both a case control study of individuals from the Milwaukee Longitudinal Study of ADHD (103 cases and 66 controls), and in 35 families composed of trios or affected sib pairs (ASP) with ADHD. Functional effects of the promoter polymorphism were tested in vitro. The non‐deleted allele was significantly more active in undifferentiated SK‐N‐MC cells compared to differentiated SK‐N‐MC and HeLa cells while a trend for increased activity for the ΔC allele was observed in undifferentiated SK‐N‐MC cells. Identification of these polymorphisms may aid future candidate gene studies in disorders with altered dopamine signaling, such as schizophrenia Parkinson's disease and ADHD. © 2004 Wiley‐Liss, Inc.