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The Role of Fluorescence in situ hybridization (FISH) in Sequencing the Tomato Genome
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Short arm Centromere Long arm
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Maize 1C = 2634 Mb Tomato 1C = 916 Mb Arabidopsis 1C = 157 Mb
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77% of the DNA is in heterochromatin 23% of DNA is in euchromatin
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77% of the DNA is in heterochromatin 23% of the DNA is in euchromatin Thus, 0.23 x 916 Mb = 211 Mb
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77% of the DNA is in heterochromatin 23% of the DNA is in euchromatin Thus, 0.23 x 916 Mb = 211 Mb Arabidopsis 1C = 157 Mb
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HindIII library 15 tomato genome equivalents 129,000 clones Averaging 117 kb
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EXPEN 2000 MolecularLinkage Map of Tomato Chromosome 10 (SGN)
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Anchor (seed) BAC LE_HBa0234C10 Probe TG285
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Anchor (seed) BAC LE_HBa0234C10 Probe TG285 aatgcctaggcatgaatcttggccatc
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Anchor (seed) BAC LE_HBa0234C10 Probe TG285 aatgcctaggcatgaatcttggccatc gctacgcttagaa
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Seed BAC LE_HBa0234C10 Probe TG285
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Seed BAC LE_HBa0234C10 Probe TG285
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Seed BAC LE_HBa0234C10 Probe TG285
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Seed BAC Contig LE_HBa0234C10 Probe TG285
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Fluorescence in situ Hybridization (FISH) China France The Netherlands Korea Japan USA
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Fluorescence in situ Hybridization (FISH) China France The Netherlands Korea Japan USA
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Nick translation biotin- digoxygenin- dinitrophenol-labeled nucleotides FISH Probes BAC DNA
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Hybridization mixture 50-100-fold excess of unlabeled tomato Cot 100 DNA Chromosomal in situ Suppression (CISS) Hybridization
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Functions of FISH in Sequencing the Tomato Genome 1. To determine the locations of anchor BACs 2. To define eu-heterochromatin borders 3. To determine distances in Mb 4. To locate problem BACs
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BAC 116C14, Slide 126, Chromosome 9, Short (p) Arm % %
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Pachytene Chromosome 9
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Pachytene chromosome 9
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Functions of FISH in Sequencing the Tomato Genome 1. To determine the locations of anchor BACs 2. To define eu-heterochromatin borders 3. To determine distances in Mb 4. To locate problem BACs
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Functions of FISH in Sequencing the Tomato Genome 1. To determine the locations of anchor BACs 2. To define eu-heterochromatin borders 3. To determine distances in Mb 4. To locate problem BACs
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Functions of FISH in Sequencing the Tomato Genome 1. To determine the locations of anchor BACs 2. To define eu-heterochromatin borders 3. To determine distances in Mb 4. To locate problem BACs
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177 BACs FISHED RESULTS SO FAR
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177 BACs FISHED 126 BACS (74%) successfully localized. RESULTS SO FAR
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177 BACs FISHED 51 failed to localize because they either gave no FISH signal or there was more than one signal in spite of CISS hybridization. 126 BACS (74%) successfully localized. RESULTS SO FAR
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Of 126 BACs localized 22 (17.5%) FISHed to wrong chromosomes
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Of 126 BACs localized 22 (17.5%) FISHed to wrong chromosomes Of these, 11 have been checked by sequencing: 7 were overgo false positives 1 was due to a picking error 1 was due to a typographical error 2 were due to mapping errors
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Of 126 BACs localized 22 (17.5%) FISHed to wrong chromosomes Of these 11 have been checked by sequencing: 7 were overgo false positives 1 were due to a picking error 1 were due to a typographical error 2 were due to mapping errors Suggesting ≤ 3% mapping errors on the EXPEN 2000 linkage map
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FUTURE ACTIVITIES an increasing emphasis on defining the size of gaps in sequencing 1) within BACs, 2) between contigs, 3) between contigs and euchromatin- heterochromatin borders
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Senior Personnel Undergraduates Lorrie Anderson Madeline Fujishiro Song-Bin Chang Lauren Larsen Suzanne Royer Dylan Westfall Lindsay Shearer Jessica Wu Steve Stack The Role of BAC Fluorescence in situ hybridization (FISH) in Sequencing the Tomato Genome
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