Genetic Polymorphism of TLR4 at Intronic Region in Guangxi Population
Wang Hai-ya
Abstract
Wang Hai-ya
Abstract
Objective To investigate the distribution of single nucleotide polymorphism( SNP) of Toll-like receptor4( TLR4) gene in Guangxi population,and to discuss the difference among various groups. Methods Polymerase chain reaction-single base extension( PCR-SBE) and DNA sequencing method were used to analyze the rs11536879A / G polymorphism of TLR4 gene at the intronic region among 196 healthy cases in Guangxi( 115 male cases,81 female cases)which was compared with the data of other 4 populations( Hapmap-CEU,Hapmap-HCB,Hapmap-JPT,Hapmap-YRI)from the Human Genome Project group( Hapmap). Results There were genotypes of AA,GA,GG in rs11536879A / G of TLR4 gene at the intronic region in Guangxi population,the frequencies of genotype and allele distribution of rs11536879A / G polymorphisms showed no significant difference between female and male groups( P 0. 05). Guangxi population showed a significant difference in the frequencies of genotype and allele distribution of rs11536879A / G polymorphism in contrast with Hapmap-CEU,Hapmap-JPT and Hapmap-YRI( P 0. 05),but showed no significant difference in contast with Hapmap-HCB( P 0. 05). Conclusion The frequencies of genotype and allele distribution of genetic polymorphisms at the TLR4 intronic region in Guangxi population show no significant difference between the male and the female,but show a significant difference among different regions and races.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To investigate the distribution of single nucleotide polymorphism( SNP) of Toll-like receptor4( TLR4) gene in Guangxi population,and to discuss the difference among various groups. Methods Polymerase chain reaction-single base extension( PCR-SBE) and DNA sequencing method were used to analyze the rs11536879A / G polymorphism of TLR4 gene at the intronic region among 196 healthy cases in Guangxi( 115 male cases,81 female cases)which was compared with the data of other 4 populations( Hapmap-CEU,Hapmap-HCB,Hapmap-JPT,Hapmap-YRI)from the Human Genome Project group( Hapmap). Results There were genotypes of AA,GA,GG in rs11536879A / G of TLR4 gene at the intronic region in Guangxi population,the frequencies of genotype and allele distribution of rs11536879A / G polymorphisms showed no significant difference between female and male groups( P 0. 05). Guangxi population showed a significant difference in the frequencies of genotype and allele distribution of rs11536879A / G polymorphism in contrast with Hapmap-CEU,Hapmap-JPT and Hapmap-YRI( P 0. 05),but showed no significant difference in contast with Hapmap-HCB( P 0. 05). Conclusion The frequencies of genotype and allele distribution of genetic polymorphisms at the TLR4 intronic region in Guangxi population show no significant difference between the male and the female,but show a significant difference among different regions and races.
Key concepts: International HapMap Project, Biology, Genotype, Single-nucleotide polymorphism, Genetics, Population, Allele, Polymorphism (computer science)