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A molecular cytogenetic analysis of chromosome behavior in Lilium ...

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Intergenomic recomb<strong>in</strong>ation and <strong>chromosome</strong> translocation <strong>in</strong> <strong>Lilium</strong> hybridsduplication <strong>in</strong>dicates that there is either a duplication or a reciprocal translocation <strong>in</strong> thepaternal parent ‘Connecticut K<strong>in</strong>g’, and <strong>in</strong> the latter, a so-called duplication-deficiencygametes has been transmitted to the progeny successfully (Burnham 1962). These twoalternative possibilities need cytological confirmation through the <strong>analysis</strong> <strong>of</strong> the Asiaticparent. From the available observations and previous reports (Abe et al. 2002; Khan 2009;Shah<strong>in</strong> et al. 2011; Van Heusden et al. 2002), it appears that the presence <strong>of</strong> a reciprocaltranslocation may be more likely. Dur<strong>in</strong>g meiosis <strong>of</strong> reciprocal translocation, quadrivalentsare normally formed at metaphase I. Chiasma formation and cross<strong>in</strong>g over <strong>in</strong> such cases willbe suppressed <strong>in</strong> the area close to the translocation breakpo<strong>in</strong>ts, both alternate and adjacentsegregation lead to reduced fertility. When progenies from these gametes are used for geneticmapp<strong>in</strong>g, markers will show skewed segregations, which has been found when these LApopulation were used for mapp<strong>in</strong>g (Shah<strong>in</strong> et al. 2011). Furthermore, two translocated<strong>chromosome</strong>s usually lead to the formation <strong>of</strong> ‘pseudol<strong>in</strong>kage’ (Albrecht and Chetelat 2009;Beeman et al. 1986; Farré et al. 2010; Kamphuis et al. 2007; Larson et al. 2011). One exampleis the l<strong>in</strong>kage maps <strong>of</strong> an <strong>in</strong>terspecific F2 Solanum ochranthum × S. juglandifolium population.Chromosome 8 and 12 were connected <strong>in</strong> one large l<strong>in</strong>kage groups, which <strong>in</strong>dicat<strong>in</strong>g a likelyreciprocal translocation (Albrecht and Chetelat 2009). In the maps <strong>of</strong> LA lily, l<strong>in</strong>kage group 1(219 cM) is more than two times longer compared with the average longth <strong>of</strong> the l<strong>in</strong>kagegrous (95 cM)(Khan 2009), which also <strong>in</strong>dicate a likely reciprocal translocation <strong>in</strong>‘Connecticut K<strong>in</strong>g’. Meanwhile, if crossovers happen <strong>in</strong> the <strong>in</strong>terstitial segment <strong>of</strong> thetranslocated <strong>chromosome</strong>, different types <strong>of</strong> duplication-deficiency gametes, which aregenerally sterile, will be produced (Fig. 3.3).In conclusion, <strong>in</strong>tergenomic recomb<strong>in</strong>ation <strong>in</strong> lily allopolyploids are derived from cross<strong>in</strong>gover events dur<strong>in</strong>g meiosis; while the non-homologous <strong>chromosome</strong> pair<strong>in</strong>g <strong>in</strong> multivalentsand bivalents potentially lead to the production <strong>of</strong> gametes with real <strong>chromosome</strong>rearrangements.43

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