the generation of chromosomal deletions to provide extensive coverage and subdivision of the drosophila melanogaster genome代的染色体缺失提供广泛的黑腹果蝇基因组覆盖率和细分.pdfVIP

the generation of chromosomal deletions to provide extensive coverage and subdivision of the drosophila melanogaster genome代的染色体缺失提供广泛的黑腹果蝇基因组覆盖率和细分.pdf

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the generation of chromosomal deletions to provide extensive coverage and subdivision of the drosophila melanogaster genome代的染色体缺失提供广泛的黑腹果蝇基因组覆盖率和细分

Cook et al. Genome Biology 2012, 13:R21 /2012/13/3/R21 RESEARCH Open Access The generation of chromosomal deletions to provide extensive coverage and subdivision of the Drosophila melanogaster genome R Kimberley Cook, Stacey J Christensen, Jennifer A Deal, Rachel A Coburn, Megan E Deal, Jill M Gresens, * Thomas C Kaufman and Kevin R Cook Abstract Background: Chromosomal deletions are used extensively in Drosophila melanogaster genetics research. Deletion mapping is the primary method used for fine-scale gene localization. Effective and efficient deletion mapping requires both extensive genomic coverage and a high density of molecularly defined breakpoints across the genome. Results: A large-scale resource development project at the Bloomington Drosophila Stock Center has improved the choice of deletions beyond that provided by previous projects. FLP-mediated recombination between FRT-bearing transposon insertions was used to generate deletions, because it is efficient and provides single-nucleotide resolution in planning deletion screens. The 793 deletions generated pushed coverage of the euchromatic genome to 98.4%. Gaps in coverage contain haplolethal and haplosterile genes, but the sizes of these gaps were minimized by flanking these genes as closely as possible with deletions. In improving coverage, a complete inventory of haplolethal and haplosterile genes was generated and extensive information on other haploinsufficient genes was compiled. To aid mapping experiments, a subset of deletions was organized into a Deficiency Kit to provide maximal coverage efficiently. To improve the resolution of deletion mapping, screens were planned to distribute deletion breakpoints evenly across the genome. The median chromosomal interval between breakpoints now contain

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