Sequence analysis of five exons of SLC6A4 gene in Mexican patients with anorexia nervosa and bulimia nervosa
| Autor: | A. Caballero-Romo, B. Camarena-Medellin, M. Flores-Ramos, L. González-Macías, A. Aguilar-García, D. Luna Dominguez, G. Flores-Flores, A. Azaola-Espinosa, S. Hernández-Muñoz |
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| Rok vydání: | 2019 |
| Předmět: |
0301 basic medicine
Anorexia Nervosa Adolescent Sequence analysis Anorexia Biology 03 medical and health sciences Exon Young Adult 0302 clinical medicine Genetics medicine Coding region Humans Genetic Predisposition to Disease Bulimia Nervosa Gene Serotonin Plasma Membrane Transport Proteins Bulimia nervosa General Medicine Exons medicine.disease Eating disorders 030104 developmental biology Anorexia nervosa (differential diagnoses) 030220 oncology & carcinogenesis Case-Control Studies Female medicine.symptom |
| Zdroj: | Gene. 748 |
| ISSN: | 1879-0038 |
| Popis: | Background Accumulating evidence indicates that alterations in the serotonin system are related to changes in eating behavior. The serotonin transporter is encoded by the SLC6A4 gene and has been an interesting candidate for anorexia nervosa- restrictive type (AN-R) and bulimia nervosa (BN). Interestingly, functional variants have been identified in the coding region that could contribute to understand the role of this gene in eating disorders. The aim was to identify genetic variants in five exons of SLC6A4 gene using Sanger-sequencing in anorexia nervosa-restrictive and bulimia nervosa patients, and a control group. Method The sample consisted of 86 patients and 50 control subjects. We obtained DNA samples from all subjects and performed Sanger-sequence analysis of the 1, 2, 3, 8 and 9 exons. The sequences were compared with the reference sequence of the SLC6A4 gene. Results The sequence analysis of the five exons of the gene identified several variants. In the AN-R, we observed two novel variants (g.130delA and c.1740G > A), three synonymous variants (rs57172732, rs55908624, rs74478645) and a missense variant (L90F) reporting a probably deleterious and damaging variant. In BN, we identified two novel variants (g.295C > G and c.1725G > A), and the non-synonymous (rs28914832/I425V), reported as benign. Interestingly, we observed the 425V variant in three patients in the BN, variant that previously was reported in patients with a spectrum obsessive–compulsive disorder. Conclusion The results of our study suggest that variants of the SLC6A4 gene are related with a possible damaging or gain-of-function and may be involved in the susceptibility to AN-R and BN patients. However, the present findings should be considered as preliminary until replicated in large samples. |
| Databáze: | OpenAIRE |
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