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The study of angiotensinogen gene polymorphism by microchip electrophoresis

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Objective To investigate the AGT gene polymorphism distribution and the relationship between the AGT gene polymorphism and essential hypertension (EH) in Shenyang Hans population using the new microchip-based method, and to develop a microchip-bases electrophoretic method for rapid detection of genotype. Method One hundred and twenty-three patients with EH and one hundred and three controls recruited from Shenyang Hans population were examined. The gene polymorphisms of AGT (G(-6)A) was determined by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) with microchip electrophoresis and agarose gel electrophoresis. Result (1) Microchip electrophoresis can separate PCR products of AGT gene within 250s. (2) The A allele frequency was very high in both groups (control: 0.7038, hypertensive: 0.7073), it was almost identical in the different groups (χ2=0.024, p>0.05), there was also no significant difference in frequencies of the allele of G(-6)A between Shenyang and Tibetan population (p>0.05). Conclusion (1) In comparison with gel electrophoresis, the new microchip-based method has distinct features such as high seperation efficiency, smaller sample volume requirement, high-throughput application as well as the sensitivity of detection. (2) Shenyang Hans population has a higher frequency of A allele in AGT gene (-6)site. G/A polymorphism exists at locus -6 of human AGT gene, which is not linked to hypertension in Shenyang Han people.
Title: The study of angiotensinogen gene polymorphism by microchip electrophoresis
Description:
Objective To investigate the AGT gene polymorphism distribution and the relationship between the AGT gene polymorphism and essential hypertension (EH) in Shenyang Hans population using the new microchip-based method, and to develop a microchip-bases electrophoretic method for rapid detection of genotype.
Method One hundred and twenty-three patients with EH and one hundred and three controls recruited from Shenyang Hans population were examined.
The gene polymorphisms of AGT (G(-6)A) was determined by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) with microchip electrophoresis and agarose gel electrophoresis.
Result (1) Microchip electrophoresis can separate PCR products of AGT gene within 250s.
(2) The A allele frequency was very high in both groups (control: 0.
7038, hypertensive: 0.
7073), it was almost identical in the different groups (χ2=0.
024, p>0.
05), there was also no significant difference in frequencies of the allele of G(-6)A between Shenyang and Tibetan population (p>0.
05).
Conclusion (1) In comparison with gel electrophoresis, the new microchip-based method has distinct features such as high seperation efficiency, smaller sample volume requirement, high-throughput application as well as the sensitivity of detection.
(2) Shenyang Hans population has a higher frequency of A allele in AGT gene (-6)site.
G/A polymorphism exists at locus -6 of human AGT gene, which is not linked to hypertension in Shenyang Han people.

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