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some (arm)-specific library is composed of a manageable number of clones, and so represents a practical tool in the area of wheat genomics. Copyright © 2010 S. Karger AG, Basel Hexaploid wheat ( Triticum aestivum L., 2n = 42) provides a source of staple food for 35% of the world's population, a...

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Bibliographic Details
Main Authors: J Šafář, H Šimková, M Kubaláková, J Číhalíková, P Suchánková, J Bartoš, J Doležel
Other Authors: The Pennsylvania State University CiteSeerX Archives
Format: Text
Language:English
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Online Access:http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.1074.8079
http://www.ueb.cas.cz/cs/system/files/users/public/Suchankova_79/625.pdf
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Summary:some (arm)-specific library is composed of a manageable number of clones, and so represents a practical tool in the area of wheat genomics. Copyright © 2010 S. Karger AG, Basel Hexaploid wheat ( Triticum aestivum L., 2n = 42) provides a source of staple food for 35% of the world's population, an importance challenged only by rice. Annual global wheat consumption exceeds 600 Mt (http://www. fao.org/), equivalent to about 100 kg per capita. Wheat is cultivated over a wide range of climates and soil conditions, from as far north as the Arctic Circle to as far south as the equator. Despite its major socio-economic importance and the current challenges faced by agriculture Abstract The large bread wheat genome (1C ϳ 17 Gbp) contains a preponderance of repetitive DNA and the species is polyploid. These characteristics together serve to hamper the molecular analysis of the wheat genome. Its complexity can, however, be reduced by using flow cytometry to isolate individual chromosomes, and these can be exploited to construct chromosome-specific BAC libraries. Such libraries simplify the task of physical map construction, positional cloning and the targeted development of genetic markers. Rapid improvements in the efficiency and cost of DNA sequencing provide an opportunity to contemplate sequencing the wheat genome by preparing sequence-ready physical maps for each chromosome or chromosome arm in turn. The quality of the chromosome-specific libraries depends on their chromosome coverage and the mean insert size. First-generation libraries suffered from a relatively low mean insert size, but improvements to the protocol have generated a second wave of libraries with a significantly increased mean insert size and better chromosome coverage. Each chromo-