한국인 기관지 천식 虛證, 實證 환자와 CD46 유전자 다형성과의 관계
Exonic SNP (rs7144, 3’-UTR) in CD46 Molecule and Complement Regulatory Protein (CD46) Gene Associated with Excess Syndrome to Categorize Korean Bronchial Asthma Patients
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Objectives: In this study, we divided Korean asthma patients into excess syndrome or deficiency syndrome groups according to clinical phenotype. Genetic analysis was conducted to investigate the association of exonic SNPs in the CD46 gene polymorphism with the clinical phenotype based on the differentiation syndrome of the bronchial asthma patients. Methods: There were 95 healthy patients (control group) and 53 asthma patients. (The deficiency syndrome group included 24 and the excess syndrome group 29). We searched the exonic areas of the CD46 gene in the NCBI website SNPs with <0.01 minor allele frequency (MAF) and <0.01 heterozygosity. We finally selected two SNPs: rs138843816, Ser13Phe and rs7144, 3’-UTR. Hardy-Weinberg equilibrium was calculated using SNPStats. Results: There were significant differences in the codominant 1 model and the dominant model between the healthy group and the asthma group. There were significant differences between deficiency syndrome group and the excess syndrome group in the genotype frequencies and in the codominant 1 model, the dominant model, and the log-additive model. The allele frequency of rs7144C showed a significant difference between the deficiency syndrome group and the excess syndrome group. Two-SNP haplotype analysis showed a significant difference in frequency in the deficiency syndrome group and in the excess syndrome group. There were significant differences between the healthy group and the excess syndrome group in the codominant 1 model, the dominant model, and the log-additive model. The frequency of the rs7144 C allele exhibited a significant difference in the demonstration. SNP haplotype analysis between the healthy group and the excess syndrome group showed a significant difference in the frequency of the CT haplotype and the CC haplotype. Conclusions: The results indicate that two CD46 SNPs (rs138843816, Ser13Phe and rs7144, 3'-UTR) might be associated with the symptomatic excess syndrome in Korean asthma patients.
Abstract
Objectives: In this study, we divided Korean asthma patients into excess syndrome or deficiency syndrome groups according to clinical phenotype. Genetic analysis was conducted to investigate the association of exonic SNPs in the CD46 gene polymorphism with the clinical phenotype based on the differentiation syndrome of the bronchial asthma patients. Methods: There were 95 healthy patients (control group) and 53 asthma patients. (The deficiency syndrome group included 24 and the excess syndrome group 29). We searched the exonic areas of the CD46 gene in the NCBI website SNPs with <0.01 minor allele frequency (MAF) and <0.01 heterozygosity. We finally selected two SNPs: rs138843816, Ser13Phe and rs7144, 3’-UTR. Hardy-Weinberg equilibrium was calculated using SNPStats. Results: There were significant differences in the codominant 1 model and the dominant model between the healthy group and the asthma group. There were significant differences between deficiency syndrome group and the excess syndrome group in the genotype frequencies and in the codominant 1 model, the dominant model, and the log-additive model. The allele frequency of rs7144C showed a significant difference between the deficiency syndrome group and the excess syndrome group. Two-SNP haplotype analysis showed a significant difference in frequency in the deficiency syndrome group and in the excess syndrome group. There were significant differences between the healthy group and the excess syndrome group in the codominant 1 model, the dominant model, and the log-additive model. The frequency of the rs7144 C allele exhibited a significant difference in the demonstration. SNP haplotype analysis between the healthy group and the excess syndrome group showed a significant difference in the frequency of the CT haplotype and the CC haplotype. Conclusions: The results indicate that two CD46 SNPs (rs138843816, Ser13Phe and rs7144, 3'-UTR) might be associated with the symptomatic excess syndrome in Korean asthma patients.
참고문헌 (43)
- 대한 결핵 및 호흡기학회, "호흡기학", pp.325~326 (2007), 군자출판사
- Masoli M, "The global burden of asthma: executive summary of the GINA Dissemination Committee report", Allergy, 59(5), pp.469~ (2004)
- 박춘식, "천식의 유전적 병인", Tuberculosis and Respiratory Diseases, 60(4), pp.391~396 (2006), 대한결핵및호흡기학회
- Meyers DA, "Genetics of asthma and allergy:what have we learned?", J Allergy Clin Immunol, 126(3), pp.439~446 (2010)
- Yao TC, "The RANTES promotor polymorphism:a genetic risk factor for near-fatal asthma in Chinese children", J Allergy Clin Immunol, 111(6), pp.1285~1292 (2003)
- Sohn MH, "RANTES gene promoter polymorphisms are associated with bronchial hyperresponsiveness in Korean children with asthma", Lung, 186(1), pp.37~43 (2008)
- 황우석, "한국인 천식환자의 Monocyte chemoattractant protein 1(MCP-1) 유전자 다형성에 대한 분석", 대한한방내과학회지, 29(1), pp.32~41 (2008), 대한한방내과학회
- 유승렬, "한국인 기관지 천식 환자에서 허실변증과 Glutathione-S-Transferase 유전자의 다형성 연구", 대한한방내과학회지, 28(3), pp.453~463 (2007), 대한한방내과학회
- 이종극, "질병유전체분석법 2", pp.113~114 (2010), 월드사이언스
- American Thoracic Society, "Guidelines for methacholine and exercise challenge testing-1999", Am J Respir Crit Care Med, 161(1), pp.309~329 (2000)
- 최준용, "기관지 천식환자의 허실변증에 따른 청상보하탕의 임상효과", 대한한방내과학회 추계학술대회논문집, pp.91~99 (2003)
- 최준용, "虛實辨證과 加味淸上補下湯의 임상효과", 대한한방내과학회지, 25(3), pp.379~387 (2004), 대한한방내과학회
- Ivaschenko TE, "Glutathione-S-tranferase micro and theta gene polymorphisms as new risk factors of atopic bronchial asthma", J Mol Med, 80(1), pp.39~43 (2002)
- Venter JC, "The sequence of the human genome", Science, 291(5507), pp.1304~1351 (2001)
- Lander ES, "Initial sequencing and analysis of the human genome", Nature, 409, pp.860~921 (2001)
- Wechsler ME, "How pharmacogenomics will play a role in the management of asthma", Am J Respir Crit Care Med, 172(1), pp.12~18 (2005)
- Edfors-Lub M, "Allergy in 7000 twin pairs", Acta Allergol, 26(4), pp.249~285 (1971)
- Burrows B, "Relation of the course of bronchial responsiveness from age 9to age 15 to allergy", Am J Respir Crit Care Med, 152(4), pp.1302~1308 (1995)
- Bousquet J, "Eosinophil inflammation in asthma", Am J Respir Crit Care Med, 150(5 Pt 2), pp.33~38 (1994)
- Vercelli D, "Genetic polymorphism in allergy and asthma", Curr opin Immunol, 15(6), pp.609~613 (2003)
- 김상헌, "Leukotriene C4 Synthase 유전자 Promoter 부위 유전적 다형과 아스피린 과민성 천식의 연관성", 천식 및 알레르기, 26(2), pp.115~121 (2006), 대한천식알레르기학회
- Jung SK, "An Angiotensi n I converting enzyme polymorphism is associated with clinical phenotype when using differentiation-syndrome to categorize korean bronchial asthma patients", Evid Based Complement Alternat Med, pp.498138~ (2011)
- Karam RA, "Impact of gluthation-S-transferase gene polymorphisms on enzyme activity, lung function and bronchial asthma susceptibility in Egyptian children", Gene, 497(2), pp.314~319 (2012)
- Daneshmandi S, "Cytokine gene polymorphism and asthma susceptibility, progress and control level", Mol Biol Rep, 39(2), pp.1845~1853 (2012)
- Tsai YG, "Functional defect of CD46-induced regulatory T cells to suppress airway inflammation mite allergic asthma", Laboratory investigation, 92, pp.1260~1269 (2012)
- J Cardone, "CD46 in innate and adaptive immunity", Clinical and Experimental Immunology, 164(3), pp.301~311 (2011)
- Seya T, "Functional properties of membranes of actoprotein of complement", Biochem J, 264, pp.581~ (1989)
- Liszewski MK, "Membrane cofactor protein(MCP orCD46): newest member of the regulators of complement activation gene cluster", Annu Rev Immunol, 9, pp.431~455 (1996)
- Liszewski MK, "Membranec of actorprotein(MCP;CD46). Isoforms differ in protection against the classical pathway of complement", J Immunol, 156(11), pp.4415~4421 (1996)
- Reid KBM, "Structure-function relationships of complement components", Immunol Today, 10(6), pp.177~180 (1989)
- Pollard AJ, "A novel isoform of human membrane cofactor protein(CD46) mRNA generated by intronretention", Gene, 212(1), pp.39~47 (1998)
- Frolikova M, "Role of complement regulatory proteins CD46, CD55and CD59 in reproduction", Folia Zoologica, 61(1), pp.84~94 (2012)
- Lublin DM, "Molecular cloning and chromosomal localization of human membrane cofactor protein(MCP). Evidence for inclusion in the multigene family of complementregulatory proteins", J Exp Med, 168(1), pp.181~194 (1988)
- Liszewski MK, "Dissectings it is important for complementre gulatory activity in membrane cofactor protein(MCP; CD46)", Journal of Biological Chemistry, 275(48), pp.37692~37701 (2000)
- Gerlier D, "Efficient major histocompatibility complex class II-restricted presentation of measles virus relieson hemag glutinin-mediated targeting to its cellular receptor human CD46 expressed by murine B cell", J Exp Med, 179(1), pp.353~358 (1994)
- Iwata K, "Modulation of complement regulatory function and measles virus receptor function by serinethreonine-rich domains of membrane cofactor protein(CD46)", Biochem J, 304(1), pp.169~175 (1994)
- Hara T, "Post-translational modification and intra cellular localization of a splice products of CD46 cloned from human testis: role of the intracellular domains in O-glycosylation", Immunology, 93(4), pp.546~555 (1998)
- Holmes CH, "Complementre gulatory proteins-27-at the feto-maternal interface during human placental development: distribution of CD59 by comparison with membrane cofactor protein(CD46) and decay accelerating factor(CD55)", Eur J Immunol, 22(6), pp.1579~1585 (1992)
- Truscott SM, "CD46 engagement on human CD4+T cells produces Tregulatorytype-like regulation of antimycobacterial T cell responses", Infect Immun, 78(12), pp.5295~5306 (2010)
- NiChoileain S, "CD46 processing :a means of expression", Immunobiology, 217(2), pp.169~175 (2012)
- Anne L Astier, "T-cell regulation by CD46 and its relevance in multiple sclerosis", Immunology, 124(2), pp.149~154 (2008)
- Hakulinen J, "Complement inhibitor membrane cofactor protein (MCP; CD46) is constitutively shed from cancer cell membranes in vesicles and converted by a metalloproteinase to a functionally active solubleform", Eur J Immunol, 34(9), pp.2620~2629 (2004)
- Christiansen D, "Chimeric CD46", DAF molecules reveal acryptic functional role for SCR1 of DAF in regulating complement activation, 2000, pp.37(12), 687~696
