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

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Chapter 4There are some criteria to dist<strong>in</strong>guish the bridges and fragments with respect to theirdifferent orig<strong>in</strong>s. Bridges from paracentric <strong>in</strong>version and U-type exchanges result <strong>in</strong> differentmeiotic configuration at the first meiotic division, which can be recognised through a criticalmeiotic observation. The first difference is that bridges and fragments from <strong>in</strong>versionheterozygote <strong>in</strong>volve non-sister chromatids, while U-type exchanges can happen betweenboth sister and non-sister chromatids. Another feature caused by <strong>in</strong>version is the <strong>in</strong>variablesize <strong>of</strong> the fragments. No matter where the crossover happened <strong>in</strong> the <strong>in</strong>version loop, theresultant acentric fragments should be <strong>of</strong> constant size. On the contrary, asymmetricalbivalents, fragment size variation and side arm bridges are all evidence for the occurrence <strong>of</strong>U-type exchanges. Moreover, bridges and fragments <strong>in</strong> some species and species hybrids,which had been considered to orig<strong>in</strong>ate from <strong>in</strong>version, have been proven to be derived fromU-type exchanges. In the species <strong>of</strong> Tradescantia and Paeonia brownii, “the occurrence <strong>of</strong><strong>in</strong>version was presumptive and circumstantial” and the presence <strong>of</strong> bridges and fragmentshave f<strong>in</strong>ally been expla<strong>in</strong>ed as due to U-type exchanges (Lewis and John 1963). In conclusion,<strong>in</strong>version heterozygote, as well as U-type exchanges, lead to anaphase bridg<strong>in</strong>g with differentconfiguration at meiosis.Meiotic bridges not only occur spontaneous, but can also be <strong>in</strong>duced by genomic shock,<strong>in</strong>clud<strong>in</strong>g radiation treatment and <strong>in</strong>terspecific hybridization. Radiation treatment, which isprobably the most efficient method, leads to <strong>chromosome</strong> breakage and various types <strong>of</strong>anaphase bridg<strong>in</strong>g <strong>in</strong> a number <strong>of</strong> species like <strong>Lilium</strong> longiflorum (Mitra 1958), Zea mays(Vicc<strong>in</strong>i and De Carvalho 2002), Triticum (Wu and Yu 2001) and many others. Interspecifichybridization is another cause <strong>of</strong> the dicentric bridge production <strong>in</strong> a wide range <strong>of</strong> specieshybrids like Vigna umbellate × V. m<strong>in</strong>ima (Gop<strong>in</strong>athan and Babu 1986), P<strong>in</strong>us hybrids(Saylor and Smith 1966) and so on. Interest<strong>in</strong>gly, the bridges and fragments <strong>in</strong> F1 hybridsfound between some species <strong>in</strong> the genus Chorthippus, which were once thought to haveorig<strong>in</strong>ated from paracentric <strong>in</strong>version, have been proven to arise from spontaneous<strong>chromosome</strong> breakage and reunion (Lewis and John 1966). In all <strong>of</strong> the above mentionedspecies and species hybrids, meiotic bridges were studied us<strong>in</strong>g traditional <strong>cytogenetic</strong>methods.Genomic <strong>in</strong> situ hybridization (GISH) and fluorescence <strong>in</strong> situ hybridization (FISH) havethe potential to give more conv<strong>in</strong>c<strong>in</strong>g results about the orig<strong>in</strong> <strong>of</strong> anaphase bridg<strong>in</strong>g. These twomethods, which enable the localization <strong>of</strong> labelled probes after DNA hybridization, can notonly dist<strong>in</strong>guish non-sister chromatids <strong>in</strong> hybrids and allopolyploids (GISH), but also check48

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