期刊文献+

Single Nucleotide Polymorphisms in CAPN10 Gene of Chinese People and Its Correlation With Type 2 Diabetes Mellitusin Han People of Northern China 被引量:2

Single Nucleotide Polymorphisms in CAPN10 Gene of Chinese People and Its Correlation With Type 2 Diabetes Mellitusin Han People of Northern China
下载PDF
导出
摘要 Objective To investigate the distribution of single nucleotide polymorphisms (SNPs)in CAPN10 gene in Chinese population and their relation with type 2 diabetes mellitus inHan people of Northern China. Methods CAPN10 gene was sequenced to detect SNPs indifferent nationalities of China. Five SNPs were chosen to perform case-control study andhaplotype analysis in 156 normal Han people of Northern China and 173 type 2 diabetes. OneSNP was also analyzed with transmission-disequilibrium test (TDT) and sib transmission-disequilibrium test (STDT) in 68 type 2 diabetes pedigrees (377 people). Results A totalof 40 SNPs were identified in length of 8 936bp, with an average of 1 in every 223bp. TheSNPs in CAPN10 gene did not distribute evenly and the SNPs in Chinese were different fromthose reported in Mexican American. There was no significantly statistical difference in theallele frequency of the 5 SNPs between case and control, and the haplotype frequencies inthe two groups were not significantly different. No positive results was found in TDT andSTDT analysis. Conclusions The SNP distribution of CAPN10 gene differs in differentnationalities. The studied SNPs in CAPN10 gene may not be the major susceptibility onesof type 2 diabetes mellitus in Han people of Northern China. Objective To investigate the distribution of single nucleotide polymorphisms (SNPs)in CAPN10 gene in Chinese population and their relation with type 2 diabetes mellitus inHan people of Northern China. Methods CAPN10 gene was sequenced to detect SNPs indifferent nationalities of China. Five SNPs were chosen to perform case-control study andhaplotype analysis in 156 normal Han people of Northern China and 173 type 2 diabetes. OneSNP was also analyzed with transmission-disequilibrium test (TDT) and sib transmission-disequilibrium test (STDT) in 68 type 2 diabetes pedigrees (377 people). Results A totalof 40 SNPs were identified in length of 8 936bp, with an average of 1 in every 223bp. TheSNPs in CAPN10 gene did not distribute evenly and the SNPs in Chinese were different fromthose reported in Mexican American. There was no significantly statistical difference in theallele frequency of the 5 SNPs between case and control, and the haplotype frequencies inthe two groups were not significantly different. No positive results was found in TDT andSTDT analysis. Conclusions The SNP distribution of CAPN10 gene differs in differentnationalities. The studied SNPs in CAPN10 gene may not be the major susceptibility onesof type 2 diabetes mellitus in Han people of Northern China.
作者 SunHX ZhangKX
出处 《Biomedical and Environmental Sciences》 SCIE CAS CSCD 2002年第1期75-82,共8页 生物医学与环境科学(英文版)
基金 the National Natural Science Foundation (Grant No. 30170441,39896200) 863 High Tech Project (Grant No. 2001AA221161) National 973 Project (Grant No.G1998051016) Beijing Natural Science Fund (Grant No. 7002026) the National High EducationSci
关键词 CAPN10 SNP Different nationalities in China Type 2 diabetes Associationstudy CAPN10 SNP Different nationalities in China Type 2 diabetes Associationstudy
  • 相关文献

参考文献9

  • 1[1]Horikawa, Y., Oda, N., Cox, N. J., Li, X., Orho-Melander, M., Hara, M., Hinokio, Y., Lindner, T. H., Mashima, H., Schwarz,P. E. H., Bosque-Plata, L. D., Horikawa, Y., Oda, Y., Yoshiuchi, I., Colilla, S., Polonsky, K. S., Wei, S., Concannon, P.,Iwasaki, N., Schulze, J., Baier, L., Bogardus, C., Groop, L., Boerwinkle, E., Hanis, C. L., and Bell, G. I. (2000). Genetic variation in the gene coding calpain-10 is associated with type 2 diabetes mellitus. Nature Genet. 26, 163-175. 被引量:1
  • 2[2]Hanis, C. L,, Boerwinkle, E.,Chakraborty, R., Ellsworth, D. L., Concannon, P., Stirling, B., Morrison, V. A., Wapelhorst,B., Spielman, R. S., Gogolin-Ewens, K. J,, Shephard, J. M., Williams, S. R., Risch, N., Hinds, D., lwasaki. N., Ogata, M.,Omori, Y., Petzold, C., Poetzsch, H., SchrOder H. -E.,. Schulze, J., Cox, N. J., Menzel, S., Boriraj, V. V., Chen, X., LimL. R., Lindner, T., Mereu, L. E., Wang, Y. -Q., Xiang, K., Yarnagata, K., Yang, Y., and Bell. G. I. ( 1996). A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2.Nature Genet. 13, 161-166. 被引量:1
  • 3[3]Nickerson, D. A., Tobe, V. O., and Taylor, S. (1997). Phred, Phrap, Consed. Polyphred. Reference: Polyphred: Automating the detection and genotyping of Single Nucleotide Substitution using fluorescence-based resequencing. Nucleic Acid Research. 25, 2745-2751. 被引量:1
  • 4[4]Lindblad-Toh, K., Winchester, E., Daly, M. J., Wang, D. G., Hirschhorn, J. N., Laviolette, J. -P., Ardlie, K., Reich, D. E.,Robinson, E., Sklar, P., Shah, N., Thomas, D., Fan, J. -B., Gingeras, T., Warrington. J., Patil, N., Hudson, T. J., and Lander,E. S. (2000). Large-scale discovery and genotyping of single-nucleotide polymorphisms in the mouse. Nature Genet. 24,381-386. 被引量:1
  • 5[5]Zhao, J. H., Curtis, D., and Sham, P. C. (2000). Model-free analysis and permutation tests for allelic association. Hum Hered.50, 133-139. 被引量:1
  • 6[6]Li, W. and Sadle, L. A. (1991). Low nucleotide diversity in man. Genetics. 129, 513-523. 被引量:1
  • 7[7]Nickerson, D. A., Taylor, S. L. Weiss, K. M., Clark, A. G., Hutchinson, R. G., Stengarcl, J., Salomaa, V., Vartiainen, E.,Boerwinkle, E., and Sing, C. F. ( 1998). DNA sequence diversity in a 9. 7kb region of the human lipoprotein lipase gene. Nature Genet. 19, 233-240. 被引量:1
  • 8[8]Wang, D. G., Fan, J. lB., Siao, C. J., Berno, A., Young, P., Sapolsky, R., Ghandour, G., Perkins, N., Winchester, E., Spencer,J., Kruglyak, L., Stein, L., Hsie, L., Topaloglou, T., Hubbell, E., Robinson, E., Mittmann, M., Morris, M. S., Shen. N.,Kilburn, D., Rioux, J., Nusbaum, C., Rozen, S., Hudson, T. J., Lipshutz, R., Chee, M., and Lander, E. S. (1998). Largescale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome. Science. 280,1077-1082. 被引量:1
  • 9[9]Zhao, J. Y., Wang, H., Xiong, M. M., Huang, W., Zuo, J., Chen, Z., Qiang, B. Q., Sun, Q., Li, Y. X., Liu, Q. Y., Du, W.N., Chen, J. L., Ding, W., Yuan, W. T., Zhao, Y., Xu, H. Y., Jin, L.. and Fang, F. D. (2000). The localization of type 2 diabetes susceptibility gene loci in Northern Chinese Han families. Chin Sci Bull. 45, 1792-1795. 被引量:1

同被引文献1

引证文献2

二级引证文献87

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部