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BMC Genet ; 21(1): 82, 2020 07 28.
Artigo em Inglês | MEDLINE | ID: mdl-32723293

RESUMO

BACKGROUND: Although the molecular function of wolframin remains unclear, the lack of this protein is known to cause stress in the endoplasmic reticulum. Some variants in the Wolfram Syndrome 1 gene (WFS1) were associated with various neuropsychiatric disorders in humans, such as aggressiveness, impulsivity and anxiety. RESULTS: Here we present an in silico study predicting a single nucleotide polymorphism (rs852850348) in the canine WFS1 gene which was verified by direct sequencing and was genotyped by a PCR-based technique. We found that the rs852850348 polymorphism is located in a putative microRNA (cfa-miR-8834a and cfa-miR-1838) binding site. Therefore, the molecular effect of allelic variants was studied in a luciferase reporter system that allowed assessing gene expression. We demonstrated that the variant reduced the activity of the reporter protein expression in an allele-specific manner. Additionally, we performed a behavioral experiment and investigated the association with this locus to different performance in this test. Association was found between food possessivity and the studied WFS1 gene polymorphism in the Border collie breed. CONCLUSIONS: Based on our findings, the rs852850348 locus might contribute to the genetic risk of possessivity behavior of dogs in at least one breed and might influence the regulation of wolframin expression.


Assuntos
Sítios de Ligação , Doenças do Cão/genética , Proteínas de Membrana/genética , MicroRNAs/genética , Síndrome de Wolfram/veterinária , Alelos , Animais , Cães , Feminino , Genótipo , Masculino , Polimorfismo de Nucleotídeo Único , Síndrome de Wolfram/genética
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