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Whole-Exome Sequencing Reveals an M268T Mutation in the Angiotensinogen Gene of Four Unrelated Renal Failure Patients from the Hail Region of Saudi Arabia | Abstract
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(IJMRHS)
Indexed in: ESCI (Thomson Reuters)

Abstract

Whole-Exome Sequencing Reveals an M268T Mutation in the Angiotensinogen Gene of Four Unrelated Renal Failure Patients from the Hail Region of Saudi Arabia

Author(s):Nuglozeh Edem, Fazaludeen F Mohammad, Mbikay Majambu, Hussain A Gadelkarim, Al-Hazimi Awdah and Ashankyty Ibraheem

Aims: Chronic kidney disease and renal failure are major health concerns in Saudi Arabia, especially in the Hail region. These diseases are commonly coupled with hypertension and hypercholesterolemia. Genetic factors strongly contribute to them. This study was undertaken in an effort to identify genetic variations that might contribute to renal failure in the Hail population. Methods: We performed Whole Exome Sequencing (WES) on genomic DNA of four unrelated Hail patients afflicted by renal failure. Exonic variations located in genes known to be implicated the disease were selected and validated by Sanger sequencing. Results: In all four patients, we identified a c.C803T transition in exon 2 of the angiotensinogen gene (AGT), causing an M268T amino acid substitution in the protein. All four patients were homozygous for T268 allele. Conclusion: AGT is implicated in blood pressure regulation; it contributes to normal kidney function. The M268T AGT mutation has been known to be associated with hypertension and kidney disease. Whether or not it is a determinant of the kidney failure of our patients could be established if family studies show segregation of the mutant allele with the disease. This study illustrates how WES can be used to identify candidate genetic variations for inherited kidney diseases.


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