首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Diversity arrays technology (DArT) for high-throughput profiling of the hexaploid wheat genome
Authors:Mona Akbari  Peter Wenzl  Vanessa Caig  Jason Carling  Ling Xia  Shiying Yang  Grzegorz Uszynski  Volker Mohler  Anke Lehmensiek  Haydn Kuchel  Mathew J Hayden  Neil Howes  Peter Sharp  Peter Vaughan  Bill Rathmell  Eric Huttner  Andrzej Kilian
Institution:(1) Triticarte P/L, 1 Wilf Crane Crescent, Yarralumla, Canberra, ACT, 2600, Australia;(2) Diversity Arrays P/L, 1 Wilf Crane Crescent, Yarralumla, Canberra, ACT, 2600, Australia;(3) Department of Plant Breeding, Technical University Munich, Am Hochanger 2, 85350 Freising, Germany;(4) Faculty of Sciences, University of Southern Queensland, Toowoomba, QLD, 4350, Australia;(5) Australian Grain Technologies P/L, University of Adelaide, Roseworthy, SA, 5371, Australia;(6) Value Added Wheat Cooperative Research Centre, Plant Breeding Institute, University of Sydney, PMB11, Camden, NSW, 2570, Australia;(7) Present address: Molecular Plant Breeding Cooperative Research Centre, University of Adelaide, PMB1, Glen Osmond, SA, 5064, Australia
Abstract:Despite a substantial investment in the development of panels of single nucleotide polymorphism (SNP) markers, the simple sequence repeat (SSR) technology with a limited multiplexing capability remains a standard, even for applications requiring whole-genome information. Diversity arrays technology (DArT) types hundreds to thousands of genomic loci in parallel, as previously demonstrated in a number diploid plant species. Here we show that DArT performs similarly well for the hexaploid genome of bread wheat (Triticum aestivum L.). The methodology previously used to generate DArT fingerprints of barley also generated a large number of high-quality markers in wheat (99.8% allele-calling concordance and approximately 95% call rate). The genetic relationships among bread wheat cultivars revealed by DArT coincided with knowledge generated with other methods, and even closely related cultivars could be distinguished. To verify the Mendelian behaviour of DArT markers, we typed a set of 90 Cranbrook × Halberd doubled haploid lines for which a framework (FW) map comprising a total of 339 SSR, restriction fragment length polymorphism (RFLP) and amplified fragment length polymorphism (AFLP) markers was available. We added an equal number of DArT markers to this data set and also incorporated 71 sequence tagged microsatellite (STM) markers. A comparison of logarithm of the odds (LOD) scores, call rates and the degree of genome coverage indicated that the quality and information content of the DArT data set was comparable to that of the combined SSR/RFLP/AFLP data set of the FW map.Electronic Supplementary Material Supplementary material is available in the online version of this article at and is accessible for authorized users.
Keywords:
本文献已被 PubMed SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号