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| Authors: | H. Budahn, H. Peterka, O. Schrader, S. Zhang |
| Keywords: | wide hybridization, Heterodera schachtii, FISH, RAPD |
Abstract:
In the genus Raphanus genetic resistance is present against the beet cyst nematode (Heterodera schachtii). Transfer of nematode resistance to rapeseed is desirable to convert this tolerant host plant into a resistant crop.
Nematode-resistant winter rapeseed would be of interest as an agronomically important trap crop in rotations with sugar beet.
Starting with the initial crosses oil radish x cabbage (RRRR x CCCC) and fodder radish x chinese cabbage (RRRR x AA), a trigenomic hybrid (RRAC) was developed and crossed several times with oilseed rape (AACC). This hybridization programme resulted in a basic population in which the presence of the nine individual radish chromosomes, a to i, was detected by cytogenetic and molecular methods (Peterka et al., 2004). The nematode resistance was localized to chromosome d.
After a further cross to rape, we were able to identify for each radish chromosome monosomic addition lines (MAL’s) having 38 chromosomes of oilseed rape and one individual chromosome of radish (2n = 4x = 38 + 1; MAL a to i). The added chromosomes in the nine MAL’s were cytologically detected with fluorescence in situ hybridization (FISH) using a radish-specific probe.
The MAL d was crossed with rape.
The progenies were classified with chromosome-specific RAPD/double-primer RAPD markers for presence/absence of the extra chromosome.
They were inoculated with L2 juveniles of Heterodera schachtii and cultivated under controlled conditions.
The MAL of chromosome d had the same resistance level as the radish variety used as chromosome donor whereas the plants without the radish chromosome were as susceptible as the rapeseed recipient.
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