Development of single nucleotide polymorphism (SNP) markers for use in commercial maize (Zea mays L.) germplasm

被引:0
作者
Elizabeth Jones
Wen-Chy Chu
Mulu Ayele
Julie Ho
Ed Bruggeman
Ken Yourstone
Antoni Rafalski
Oscar S. Smith
Michael D. McMullen
Chethana Bezawada
Jana Warren
Jean Babayev
Sutirtha Basu
Stephen Smith
机构
[1] Pioneer Hi-Bred International,Plant Genetics Research Unit
[2] Inc. (DuPont Agriculture and Nutrition),Division of Plant Sciences
[3] Pioneer Hi-Bred International,undefined
[4] Inc. (DuPont Agriculture and Nutrition),undefined
[5] Pioneer Hi-Bred International,undefined
[6] Inc. (DuPont Agriculture and Nutrition),undefined
[7] DuPont Agriculture and Nutrition,undefined
[8] USDA-Agricultural Research Service,undefined
[9] University of Missouri,undefined
来源
Molecular Breeding | 2009年 / 24卷
关键词
Maize; Single nucleotide polymorphisms (SNP); Illumina; Expected heterozygosity; Genetic mapping;
D O I
暂无
中图分类号
学科分类号
摘要
The development of single nucleotide polymorphism (SNP) markers in maize offers the opportunity to utilize DNA markers in many new areas of population genetics, gene discovery, plant breeding and germplasm identification. However, the steps from sequencing and SNP discovery to SNP marker design and validation are lengthy and expensive. Access to a set of validated SNP markers is a significant advantage to maize researchers who wish to apply SNPs in scientific inquiry. We mined 1,088 loci sequenced across 60 public inbreds that have been used in maize breeding in North America and Europe. We then selected 640 SNPs using generalized marker design criteria that enable utilization with several SNP chemistries. While SNPs were found on average every 43 bases in 1,088 maize gene sequences, SNPs that were amenable to marker design were found on average every 623 bases; representing only 7% of the total SNPs discovered. We also describe the development of a 768 marker multiplex assay for use on the Illumina® BeadArray™ platform. SNP markers were mapped on the IBM2 intermated B73 × Mo17 high resolution genetic map using either the IBM2 segregating population, or segregation in multiple parent-progeny triplets. A high degree of colinearity was found with the genetic nested association map. For each SNP presented we give information on map location, polymorphism rates in different heterotic groups and performance on the Illumina® platform.
引用
收藏
页码:165 / 176
页数:11
相关论文
共 142 条
  • [1] Altschul SF(1997)Gapped BLAST and PSI-BLAST: a new generation of protein database search programs Nucleic Acids Res 25 3389-3402
  • [2] Madden TL(2003)A high-throughput SNuPE assay for genotyping SNPs in flanking regions of Mol Breed 11 111-120
  • [3] Schäffer AA(2002) sequence tagged simple sequence repeats Plant Mol Biol 48 539-547
  • [4] Zhang J(2002)Insertion-deletion polymorphisms in 3’ regions of maize genes occur frequently and can be used as highly informative genetic markers BMC Genet 3 19-1502
  • [5] Zhang Z(2005)SNP frequency, haplotype structure and linkage disequilibrium in elite maize inbred lines Genome Res 15 1496-1605
  • [6] Miller W(2002)Ascertainment bias in studies of the human genome-wide polymorphism Plant Physiol 130 1598-439
  • [7] Lipman DJ(2007)Genetic, physical and informatic resources for maize: on the road to an integrated map Genetics 175 429-50
  • [8] Batley J(2005)Nearly identical paralogs: implications for maize ( Evol Bioinform Online 1 47-1326
  • [9] Mogg R(2004) L.) genome evolution Plant Physiol 134 1317-535
  • [10] Edwards D(2001)Arlequin (version 3.0): an integrated software package for population genetics data analysis Curr Sci 80 524-371