Crop Science Journal of Natural Resources and Life Sciences Education
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Published online 20 May 2008
Published in Crop Sci 48:1000-1006 (2008)
© 2008 Crop Science Society of America
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Genetic Variation and Genotype x Environment Interactions of Phytosterol Content in Three Doubled Haploid Populations of Winter Rapeseed

Samija Amar, Heiko C. Becker and Christian Möllers*

Dep. of Crop Sciences, Plant Breeding, Georg-August-Universität Göttingen, Von-Siebold-Str. 8, 37075 Göttingen, Germany

* Corresponding author (cmoelle2{at}gwdg.de).

Phytosterols are natural constituents of vegetable oils and are known for their cholesterol-lowering properties. The oil of rapeseed (Brassica napus L.) is one of the richest natural sources of phytosterols. Genetically enhancing the phytosterol content could give an added value to the rapeseed oil and derived products. Our objectives were to develop a gas-liquid chromatographic method for the analysis of phytosterol content in seeds of oilseed rape, to determine the genetic variation and the genotype x environment interactions, and to estimate correlations between phytosterols and other important seed quality traits in three doubled haploid populations of winter rapeseed. The populations were tested during several years in three to four environments. Sitosterol and campesterol were detected as the two major phytosterols followed by brassicasterol, avenasterol, and stigmasterol. Large differences were found in total phytosterol content (2.57 to 4.15 g kg–1 seed), with predominant genetic variance components resulting in high heritabilities ranging from 0.84 to 0.91. Phytosterol content was not negatively correlated with oil content and there were no close correlations to protein and glucosinolate content. The large genetic variation along with high heritabilities indicate that an effective breeding for enhanced phytosterol content and modified composition should be possible without negative impacts on oil, protein, or glucosinolate content.

Abbreviations: DH, doubled haploid • GLC, gas-liquid chromatographic


The authors gratefully acknowledge the technical assistance of Uwe Ammermann. The authors are thankful to Dr. Kemal Gül, Dr. Antje Schierholt, and Dr. Jianyi Zhao for providing the seed samples for Populations I, II, and III, as well as to Dr. Paresh Dutta (Swedish University of Agricultural Sciences, Uppsala, Sweden) and Dr. Ludger Brühl (Institute for Lipid Research, Münster, Germany) for helpful advice regarding the method and for performing analysis of a reference seed sample. Samija Amar received a scholarship from the Hans-Böckler-Stiftung.

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Received for publication October 18, 2007.





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