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人类皮肤颜色基因的SNP统计分析

Statistic analysis of SNP for human skin color gene
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摘要 与人类皮肤颜色相关的6个主导基因,依次为SLC24A5,OCA2,SLC45A2,MLPH,MC1R和ASIP,对其5’端、3’端、内含子区和CDS区进行分析,发现5-’UTR SNP为0个,皮肤颜色基因的SNP发生的频率为每598个碱基一个,属于转换型变异的SNP约占全部SNP的2/3.充分证明人类皮肤颜色基因区5-’UTR是极为保守的,但CDS区却为SNP的高发区.同时通过四类人群肤色基因的SNP差异程度来构建他们的亲源关系,最近的亲源关系存在于中国人与日本人间. Six dominant genes related to human skin color are SLC24A5, OCA2, SLG45A2. MLPH, MC1R and ASIP, among which, the 5'-end, the 3' -end, and regions of intron and CDS were analyzed. It was found that the count of SNP of 5' -UTR is 0, the frequency of SNP in skin color gene was one every 598 base pairs, the frequency of transit/on ~or all SNP was about 2/3. It was fully proved that 5 '-UTR o~ human skin color gene was extremely conservative. However, the frequency of SNP in CDS was extremely high. Simultaneity homology was constructed by the degree of difference in skin color genes, and the closest homology was found between Chinese and Japanese.
出处 《内蒙古科技大学学报》 CAS 2007年第4期345-348,共4页 Journal of Inner Mongolia University of Science and Technology
基金 国家自然科学基金资助项目(60761001) 内蒙古自然科学基金重点资助项目(200508010102)
关键词 SNP 皮肤颜色基因 颠换 转换 统计分析 SNP skin color genes transversion transition statistical analysis
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  • 1[1]Nielsen R. Population genetic analysis of ascertained SNP data.Hum Genomics ,2004 ,1: 218-22 4.
  • 2[2]Romkes M, Buch SC. Genotyping technologies: application to biotransformation enzyme genetic polymorphism screening. Methods Mol Biol,2005,291:399-414.
  • 3[3]Kaji N, Baba Y. Microchip technology for SNPs analysis and proteomics. Seikagaku, 2004,76:1275-1282.
  • 4[4]Twyman RM. SNP discovery and typing technologies for pharmacogenomics. Curr Top Med Chem,2004,4:1423-1431.
  • 5[5]Ishikawa M. Physical mapping of single-molecule DNA structures,Tanpakushitsu Kakusan Koso ,2004,49: 1490-1494.
  • 6[6]Stram DO . Tag SNP selection for association studies. Genet Epidemiol,2004,27:365-374.
  • 7[7]Belmont JW, Gibbs RA. Genome-wide linkage disequilibrium and haplotype maps. Am J Pharmacogenomics ,2004,4:253-262.
  • 8[8]Dearlove AM. High throughput genotyping technologies. Brief Funct Genomic Proteomic ,2002,1:139-150.
  • 9[9]Gabrielle S. Sellick, 1 Christine Garrett, et al. A Novel Gene for Neonatal Diabetes Maps to Chromosome 10p12.1-p13. DIABETES,2003,52:2636-2638.
  • 10[10]Bertram L, Hiltunen M, Parkinson M et al. Family-based association between Alzheimer's disease and variants in UBQLN1. N Engl J Med,2005 352: 884-894.

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