Seven SNPs in the Coding Sequence of Leptin Receptor Gene in Long-term Selected Japanese Quail Lines

The objective of this study was to identify SNPs in the coding sequence of the leptin receptor gene and to test for their possible association with 20 economically advantageous traits in 15 generations of 2 selected (HBW and LBW) and a control of japanase quail. A 350-bp part of the leptin receptor coding region was amplified and sequenced and understood that the fragment contained 7 SNPs (GenBank: KP674322.1-KP674328.1) that were detected in 5 loci (T3216C, T3265C, T3265G, C3265G, T3303C, A3311G, and T3347C) in a total of 30 individuals. The T3216C and T3303C SNPs located at the end of the codon were synonymous and did not affect the presence of proline. However, phenylalanine, leucine and valine were produced when the T3265C, T3265G and C3265G SNPs, respectively, were present. Glutamine or arginine was produced when the A3311G SNP was A or G, respectively, and serine was produced when the T3347C SNP was C. Although codons and amino acid sequences changed due to the second SNP, the secondary protein structure was not changed. However, the fourth and fifth SNPs changed both the amino acid sequences and secondary protein structure.\n\nPairing the SNP loci with phenotypic traits created haplogroups. When all individuals were evaluated together, some of the differences between the haplogroups were statistically significant (p<0.05; p<0.01). These results showed that both the sequence and structure of the leptin receptor gene could be altered by long-term selection. However, to achieve a more precise understanding of the role of leptin, entire coding sequences of leptin and the leptin receptor should be studied.