AUTHOR=Iino Kyoka , Toriumi Kazuya , Agarie Riko , Miyashita Mitsuhiro , Suzuki Kazuhiro , Horiuchi Yasue , Niizato Kazuhiro , Oshima Kenichi , Imai Atsushi , Nagase Yukihiro , Kushima Itaru , Koike Shinsuke , Ikegame Tempei , Jinde Seiichiro , Nagata Eiichiro , Washizuka Shinsuke , Miyata Toshio , Takizawa Shunya , Hashimoto Ryota , Kasai Kiyoto , Ozaki Norio , Itokawa Masanari , Arai Makoto TITLE=AKR1A1 Variant Associated With Schizophrenia Causes Exon Skipping, Leading to Loss of Enzymatic Activity JOURNAL=Frontiers in Genetics VOLUME=12 YEAR=2021 URL=https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2021.762999 DOI=10.3389/fgene.2021.762999 ISSN=1664-8021 ABSTRACT=
Schizophrenia is a heterogeneous psychiatric disorder characterized by positive symptoms such as hallucinations and delusions, negative symptoms such as anhedonia and flat affect, and cognitive impairment. Recently, glucuronate (GlucA) levels were reported to be significantly higher in serum of patients with schizophrenia than those in healthy controls. The accumulation of GlucA is known to be related to treatment-resistant schizophrenia, since GlucA is known to promote drug excretion by forming conjugates with drugs. However, the cause of GlucA accumulation remains unclear. Aldo-keto reductase family one member A1 (AKR1A1) is an oxidoreductase that catalyzes the reduction of GlucA. Genetic loss of AKR1A1 function is known to result in the accumulation of GlucA in rodents. Here, we aimed to explore genetic defects in