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State-of-the-art and novel developments of in vivo haploid technologies

Zugehörigkeit
Biochemie-Zentrum Regensburg, University of Regensburg, Universitätsstraße 31, Regensburg, Germany
Kalinowska, Kamila;
Zugehörigkeit
Leibniz Institute of Plant Genetics and Crop Plant Research (IPK) Gatersleben, Corrensstraße 3, Stadt Seeland, Germany
Chamas, Sindy;
GND
1172354170
Zugehörigkeit
Institute for Breeding Research on Horticultural Crops, Federal Research Centre for Cultivated Plants, Julius Kühn-Institute (JKI), Erwin-Baur-Str. 27, Quedlinburg, Germany
Unkel, Katharina;
Zugehörigkeit
Leibniz Institute of Plant Genetics and Crop Plant Research (IPK) Gatersleben, Corrensstraße 3, Stadt Seeland, Germany
Demidov, Dmitri;
Zugehörigkeit
Leibniz Institute of Plant Genetics and Crop Plant Research (IPK) Gatersleben, Corrensstraße 3, Stadt Seeland, Germany
Lermontova, Inna;
Zugehörigkeit
Biochemie-Zentrum Regensburg, University of Regensburg, Universitätsstraße 31, Regensburg, Germany
Dresselhaus, Thomas;
Zugehörigkeit
Leibniz Institute of Plant Genetics and Crop Plant Research (IPK) Gatersleben, Corrensstraße 3, Stadt Seeland, Germany
Kumlehn, Jochen;
GND
1059150336
Zugehörigkeit
Institute for Breeding Research on Horticultural Crops, Federal Research Centre for Cultivated Plants, Julius Kühn-Institute (JKI), Erwin-Baur-Str. 27, Quedlinburg, Germany
Dunemann, Frank;
Zugehörigkeit
Leibniz Institute of Plant Genetics and Crop Plant Research (IPK) Gatersleben, Corrensstraße 3, Stadt Seeland, Germany
Houben, Andreas

The ability to generate (doubled) haploid plants significantly accelerates the crop breeding process. Haploids have been induced mainly through the generation of plants from cultivated gametophic (haploid) cells and tissues, i.e., in vitro haploid technologies, or through the selective loss of a parental chromosome set upon inter- or intraspecific hybridization. Here, we focus our review on the mechanisms responsible for the in vivo formation of haploids in the context of inter- and intraspecific hybridization. The application of a modified CENH3 for uniparental genome elimination, the IG1 system used for paternal as well as the BBM-like and the patatin-like phospholipase essential for maternal haploidy induction are discussed in detail.

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