Multiplex SNP genotyping in pooled DNA samples by a four-colour microarray system.

We selected 125 candidate single nucleotide polymorphisms (SNPs) in genes belonging to the human type 1 interferon (IFN) gene family and the genes coding for proteins in the main type 1 IFN signalling pathway by screening databases and by in silico comparison of DNA sequences. Using quantitative analysis of pooled DNA samples by solid-phase mini-sequencing, we found that only 20% of the candidate SNPs were polymorphic in the Finnish and Swedish populations. To allow more effective validation of candidate SNPs, we developed a four-colour microarray-based mini-sequencing assay for multiplex, quantitative allele frequency determination in pooled DNA samples. We used cyclic mini-sequencing reactions with primers carrying 5'-tag sequences, followed by capture of the products on microarrays by hybridisation to complementary tag oligonucleotides. Standard curves prepared from mixtures of known amounts of SNP alleles demonstrate the applicability of the system to quantitative analysis, and showed that for about half of the tested SNPs the limit of detection for the minority allele was below 5%. The microarray-based genotyping system established here is universally applicable for genotyping and quantification of any SNP, and the validated system for SNPs in type 1 IFN-related genes should find many applications in genetic studies of this important immunoregulatory pathway.

[1]  L Peltonen,et al.  Minisequencing: a specific tool for DNA analysis and diagnostics on oligonucleotide arrays. , 1997, Genome research.

[2]  S. P. Fodor,et al.  Blocks of Limited Haplotype Diversity Revealed by High-Resolution Scanning of Human Chromosome 21 , 2001, Science.

[3]  A Chakravarti,et al.  Parallel genotyping of human SNPs using generic high-density oligonucleotide tag arrays. , 2000, Genome research.

[4]  Andres Metspalu,et al.  Evaluating the arrayed primer extension resequencing assay of TP53 tumor suppressor gene , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[5]  N. Gerry,et al.  Universal DNA microarray method for multiplex detection of low abundance point mutations. , 1999, Journal of molecular biology.

[6]  H. Lehrach,et al.  A novel procedure for efficient genotyping of single nucleotide polymorphisms. , 2000, Nucleic acids research.

[7]  M. Daly,et al.  A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms , 2001, Nature.

[8]  P. S. White,et al.  Flow cytometry-based minisequencing: a new platform for high-throughput single-nucleotide polymorphism scoring. , 2000, Genomics.

[9]  M. Weiner,et al.  A microsphere-based assay for multiplexed single nucleotide polymorphism analysis using single base chain extension. , 2000, Genome research.

[10]  O. Olopade,et al.  Scaffold-associated regions in the human type I interferon gene cluster on the short arm of chromosome 9. , 1998, Genomics.

[11]  C. Richardson,et al.  A single residue in DNA polymerases of the Escherichia coli DNA polymerase I family is critical for distinguishing between deoxy- and dideoxyribonucleotides. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[12]  C. Bogdan The function of type I interferons in antimicrobial immunity. , 2000, Current opinion in immunology.

[13]  G. Stark,et al.  How cells respond to interferons. , 1998, Annual review of biochemistry.

[14]  C. Sabatti,et al.  Dissecting a population genome for targeted screening of disease mutations. , 2001, Human molecular genetics.

[15]  Katarina Lindroos,et al.  Minisequencing on oligonucleotide microarrays: comparison of immobilisation chemistries , 2001, Nucleic Acids Res..

[16]  J. V. Moran,et al.  Initial sequencing and analysis of the human genome. , 2001, Nature.

[17]  L. Rönnblom,et al.  A Pivotal Role for the Natural Interferon α–producing Cells (Plasmacytoid Dendritic Cells) in the Pathogenesis of Lupus , 2001, The Journal of experimental medicine.

[18]  U. Landegren,et al.  Determination of the frequencies of ten allelic variants of the Wilson disease gene (ATP7B), in pooled DNA samples , 2000, European Journal of Human Genetics.

[19]  K. Lindblad-Toh,et al.  SBE-TAGS: an array-based method for efficient single-nucleotide polymorphism genotyping. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[20]  A Sajantila,et al.  Identification of individuals by analysis of biallelic DNA markers, using PCR and solid-phase minisequencing. , 1993, American journal of human genetics.

[21]  M. Fellous,et al.  The amino-terminal region of Tyk2 sustains the level of interferon alpha receptor 1, a component of the interferon alpha/beta receptor. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[22]  Pui-Yan Kwok,et al.  Single-nucleotide polymorphisms in the public domain: how useful are they? , 2001, Nature Genetics.

[23]  A. Syvänen From gels to chips: “Minisequencing” primer extension for analysis of point mutations and single nucleotide polymorphisms , 1999, Human mutation.

[24]  L. Kruglyak Prospects for whole-genome linkage disequilibrium mapping of common disease genes , 1999, Nature Genetics.

[25]  L. Peltonen,et al.  A system for specific, high-throughput genotyping by allele-specific primer extension on microarrays. , 2000, Genome research.

[26]  M. David,et al.  Distinct mechanisms of STAT phosphorylation via the interferon-alpha/beta receptor. Selective inhibition of STAT3 and STAT5 by piceatannol. , 2000, The Journal of biological chemistry.

[27]  Erik L. L. Sonnhammer,et al.  A workbench for large-scale sequence homology analysis , 1994, Comput. Appl. Biosci..

[28]  A. Metspalu,et al.  Arrayed primer extension: solid-phase four-color DNA resequencing and mutation detection technology. , 2000, Genetic testing.

[29]  L. Rönnblom,et al.  An etiopathogenic role for the type I IFN system in SLE. , 2001, Trends in immunology.

[30]  J. Ott,et al.  Trimming, weighting, and grouping SNPs in human case-control association studies. , 2001, Genome research.

[31]  R. Strausberg,et al.  High-throughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[32]  U Hammerling,et al.  Determination of single-nucleotide polymorphisms by real-time pyrophosphate DNA sequencing. , 2000, Genome research.

[33]  Gabor T. Marth,et al.  A general approach to single-nucleotide polymorphism discovery , 1999, Nature Genetics.