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Applications of advanced cytogenetic techniques in sugarcane

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Plant & Animal Genomes XVI Conference

January 12-16, 2008

Town & Country Convention Center

San Diego, CA

W243 : Intl. Consortium for Sugarcane Biotech. (ICSB)

Applications Of Advanced Cytogenetic Techniques In Sugarcane

Nathalie Piperidis

1, 2

, Jianwen Chen

3

, Angelique D’Hont

4

, George Piperidis

1, 2

1 BSES Limited, PMB 57, Mackay Mail Centre, Mackay, Queensland, 4741, Australia.

2 Cooperative Research Centre for Sugar Industry Innovation through Biotechnology, John Hines Building, The

University of Queensland, St Lucia Qld, 4068 Australia.

3 Guangzhou Sugar Industry Research Institute, 10 Shi Liu Gang Road, Chi Gang, Guangzhou, 510316, PR

China.

4 CIRAD, Centre de Coopération Internationale en Recherche Agronomique pour le Développement, UMR1098,

avenue Agropolis, 34398 Montpellier cedex 5, France.

Cytogenetic techniques, GISH (Genomic In Situ Hybridisation) and FISH (Fluorescence In Situ Hybridisation), are essential tools to characterize the chromosome composition and the mode of chromosome transmission in complex polyploid interspecific hybrids such as sugarcane. Four examples will be presented. i) Erianthus arundinaceus, a related genus to Saccharum is considered as having a great potential as a germplasm source for better ratoonability, vigour, tolerance to environmental stresses, and disease resistance in sugarcane. Fertile clones from intergeneric crosses between Saccharum officinarum and E. arundinaceus and two backcross generations have been generated in China. GISH was used to characterise this material and revealed n+n transmission in the I1 and the second back-cross (I3) and 2n+n transmission in the first back-cross (I2). No recombination events were observed between Saccharum and E. arundinaceus chromosomes in either I2 or I3 clones. ii) We analysed a few atypical S. officinarum clones with more than 80 chromosomes and demonstrated that they were derived from interspecific hybridization supporting classical cytogeneticist view that this species is characterized by 2n=80. iii) We conducted GISH analysis of two progeny, from a cross between S. officinarum and a cultivar (Q165,) used to generate genetic maps and revealed the occurrence of 2n+n transmission. iv) the basic number in S. officinarum and S. spontaneum is different with x=10 and x=8 respectively. We are currently mapping on the chromosomes, BAC clones anchored to the R570 genetic map, to investigate the structural difference between the chromosomes of these two species.

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