Unveiling polymorphism and protein structure prediction insights in diacylglycerol O-acyltransferase 1 and telethonin genes of Egyptian buffalo
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Published:2024-02-29
Issue:1
Volume:85
Page:
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ISSN:2090-990X
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Container-title:The Journal of Basic and Applied Zoology
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language:en
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Short-container-title:JoBAZ
Author:
Helalia Sahar M., El Makawy Aida I.ORCID, Ali Neama I., Hassan Nagwa H. A., Hassanane Mohamed S.
Abstract
Abstract
Background
The Egyptian buffalo has a sizable impact on Egypt's agricultural sector and food supply. It is regarded as the main dairy animal and an important source of red meat. This study aimed to detect the polymorphisms of the DGAT1 and TCAP genes and assess the potential impact of the discovered nsSNPs on the stability of the tertiary structure polypeptides of selected genes in Egyptian buffalo.
Methods
Allele identification was made by the restriction fragment length polymorphism (RFLP), and the single nucleotide polymorphisms (SNPs) were recognized by sequencing the purified PCR products. Protein translation indicated the synonymous and non-synonymous SNPs, and the peptides' 3D tertiary structure of selected genes, as well as the effect of amino acid substitution on the protein structure, was performed using bioinformatics tools.
Results
Analysis of the data revealed that an nsSNP was detected in a tested region of the DGAT1 gene and caused an amino acid substitution in a polypeptide that was predicted to be neutral and located in the coiled part of the protein. The analysis of the TCAP gene showed four nsSNPs that caused four substitutions located in the α-helix region. Protein prediction analysis showed that the amino acid substitutions in DGAT1 and TCAP were non-conserved with low sensitivity to variation. The non-conservative amino acid substitutions result in amino acids with new properties different from the original amino acid that change the protein's structure and function.
Conclusion
We can infer that the DGAT1 and TCAP genes' SNPs may affect meat-related traits and may improve meat quality.
Publisher
Springer Science and Business Media LLC
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