The ANKK1 Kinase Gene and Psychiatric Disorders

The Taq IA single nucleotide polymorphism (SNP, rs1800497), which is located in the gene that codes for the putative kinase ANKK1 ( ANKK1 ) near the termination codon of the D2 dopamine receptor gene ( DRD2 ; chromosome 11q22–q23), is the most studied genetic variation in a broad range of psychiatri...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Neurotoxicity research 2009-07, Vol.16 (1), p.50-59
Hauptverfasser: Ponce, Guillermo, Pérez-González, Rocío, Aragüés, María, Palomo, Tomás, Rodríguez-Jiménez, Roberto, Jiménez-Arriero, Miguel Angel, Hoenicka, Janet
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The Taq IA single nucleotide polymorphism (SNP, rs1800497), which is located in the gene that codes for the putative kinase ANKK1 ( ANKK1 ) near the termination codon of the D2 dopamine receptor gene ( DRD2 ; chromosome 11q22–q23), is the most studied genetic variation in a broad range of psychiatric disorders and personality traits. A large number of individual genetic association studies have found that the Taq IA SNP is linked to alcoholism and antisocial traits. In addition, it has also been related to other conditions such as schizophrenia, eating disorders, and some behavioral childhood disorders. The Taq IA A1 allele is mainly associated with addictions, antisocial disorders, eating disorders, and attention-deficit/hyperactivity disorders, while the A2 allele occurs more frequently in schizophrenic and obsessive-compulsive patients. Current data show that the Taq IA polymorphism may be a marker of both DRD2 and ANKK1 genetic variants. ANKK1 would belong to a family of kinases involved in signal transduction. This raises the question of whether signaling players intervene in the pathophysiology of psychiatric disorders. Basic research on the ANKK1 protein and its putative interaction with the D2 dopamine receptor could shed light on this issue.
ISSN:1029-8428
1476-3524
DOI:10.1007/s12640-009-9046-9