scholarly journals Single Nucleotide Polymorphisms of the Angiotensin-Converting Enzyme (ACE) Gene Are Associated with Essential Hypertension and Increased ACE Enzyme Levels in Mexican Individuals

PLoS ONE ◽  
2013 ◽  
Vol 8 (5) ◽  
pp. e65700 ◽  
Author(s):  
Nancy Martínez-Rodríguez ◽  
Carlos Posadas-Romero ◽  
Teresa Villarreal-Molina ◽  
Maite Vallejo ◽  
Leonardo Del-Valle-Mondragón ◽  
...  
2015 ◽  
Vol 25 (10) ◽  
pp. 485-490 ◽  
Author(s):  
Efthimios Dardiotis ◽  
Konstantinos Paterakis ◽  
Vasileios Siokas ◽  
Georgios Tsivgoulis ◽  
Maria Dardioti ◽  
...  

2011 ◽  
Vol 21 (3) ◽  
pp. 136-141 ◽  
Author(s):  
Efthimios Dardiotis ◽  
Jeremiasz Jagiella ◽  
Georgia Xiromerisiou ◽  
Maria Dardioti ◽  
Christina Vogiatzi ◽  
...  

Author(s):  
Sergii V. Goncharov ◽  
Veronika L. Gurianova ◽  
Dmytro O. Stro ◽  
Tatyana I. Drevytska ◽  
Sergii P. Kaplinskii ◽  
...  

2002 ◽  
Vol 48 (12) ◽  
pp. 2131-2140 ◽  
Author(s):  
Chikh Bengra ◽  
Theodore E Mifflin ◽  
Yuri Khripin ◽  
Paolo Manunta ◽  
Scott M Williams ◽  
...  

Abstract Background: Human hypertension is a complex, multifactorial disease with a heritability of more than 30–50%. A genetic screening test based on analysis of multiple single-nucleotide polymorphisms (SNPs) to assess the likelihood of developing hypertension would be helpful for disease management. Methods: Tailed allele-specific primers were designed to amplify by PCR six biallelic SNP loci [three in G protein-coupled receptor kinase type 4 (GRK4): R65L, A142V, and A486V; two in angiotensinogen: −6G→A and M235T; and one in aldosterone synthase: −344C→T] associated with essential hypertension. PCRs of SNP loci were coupled (via a common sequence of 21 nucleotide tails) to incorporate Universal Amplifluor™ primers labeled with fluorescein or sulforhodamine in a homogeneous format. Use of Amplifluors in SNP PCRs produced labeled amplicons, the fluorescence of which was quantified by a microplate reader and then analyzed via an Excel macro to provide genotypes for all six SNP loci. Unique restriction endonucleases were identified for five SNP loci that could independently confirm homogeneous PCR results when needed. Results: We developed six homogeneous PCR assays that were set up, performed, and fluorometrically analyzed in 96-well microplates. Allele frequencies were determined for six SNPs in 60 Italian hypertensive patients and a control group of 60 normotensive persons. A significant correlation (P = 0.034) between one SNP [GRK4 (A486V)] and the hypertensive patients was observed. Genotyping results for five of six SNPs were confirmed by digesting corresponding amplicons with locus-specific restriction endonucleases. Conclusions: We developed a simple and homogeneous fluorescent protocol that has been used to determine the SNP genotype for six loci in a population of hypertensive and normotensive persons. We also observed a significant association (P = 0.034) between one SNP (A486V) and an Italian population of mildly hypertensive patients.


2020 ◽  
Vol 15 (8) ◽  
pp. 507-514
Author(s):  
Alireza Mohebbi ◽  
Fatemeh Sana Askari ◽  
Mohsen Ebrahimi ◽  
Mana Zakeri ◽  
Mohammad Yasaghi ◽  
...  

Background: Variations in the viral receptor human angiotensin-converting enzyme 2 (ACE2) may specify the susceptibility of a certain population to severe acute respiratory syndrome coronavirus 2. Objective: Evaluation of the affinity of severe acute respiratory syndrome coronavirus 2 spike glycoprotein to the Iranian genetic variants of ACE2. Materials & methods: Single nucleotide polymorphisms of ACE2 among the Iranian population were collected from the Iranome database. Missense mutations in the N-terminal peptidase domain were selected for in silico analysis. Results: 17 missense single nucleotide polymorphisms were found at ACE2. Viral glycoprotein had the lowest affinity to ACE2 mutant V485L. Discussion: The V485L variant of ACE2 could be a natural resistance mutation among the Iranian population. In addition, variant S331F can increase slightly the susceptibility to infection with the virus.


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