Detection of genomic deletions in rice using oligonucleotide microarrays

被引:23
作者
Bruce, Myron [1 ]
Hess, Ann [2 ]
Bai, Jianfa [3 ]
Mauleon, Ramil [4 ]
Diaz, M. Genaleen [1 ,5 ]
Sugiyama, Nobuko [4 ]
Bordeos, Alicia [4 ]
Wang, Guo-Liang [6 ]
Leung, Hei [4 ]
Leach, Jan E. [1 ]
机构
[1] Colorado State Univ, Dept Bioagr Sci & Pest Management, Program Plant Mol Biol, Ft Collins, CO 80523 USA
[2] Colorado State Univ, Dept Stat, Ft Collins, CO 80523 USA
[3] Kansas State Univ, Gene Express Facil, Manhattan, KS 66506 USA
[4] Int Rice Res Inst, Manila 1099, Philippines
[5] Univ Philippines, Inst Biol Sci, Los Banos, Philippines
[6] Ohio State Univ, Dept Plant Pathol, Columbus, OH 43210 USA
来源
BMC GENOMICS | 2009年 / 10卷
关键词
FEATURE POLYMORPHISM DISCOVERY; FUNCTIONAL GENOMICS; GENE-EXPRESSION; HYBRIDIZATION; SYSTEM; MUTANT; MUTATIONS; BARLEY;
D O I
10.1186/1471-2164-10-129
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: The induction of genomic deletions by physical- or chemical-agents is an easy and inexpensive means to generate a genome-saturating collection of mutations. Different mutagens can be selected to ensure a mutant collection with a range of deletion sizes. This would allow identification of mutations in single genes or, alternatively, a deleted group of genes that might collectively govern a trait (e. g., quantitative trait loci, QTL). However, deletion mutants have not been widely used in functional genomics, because the mutated genes are not tagged and therefore, difficult to identify. Here, we present a microarray-based approach to identify deleted genomic regions in rice mutants selected from a large collection generated by gamma ray or fast neutron treatment. Our study focuses not only on the utility of this method for forward genetics, but also its potential as a reverse genetics tool through accumulation of hybridization data for a collection of deletion mutants harboring multiple genetic lesions. Results: We demonstrate that hybridization of labeled genomic DNA directly onto the Affymetrix Rice GeneChip (R) allows rapid localization of deleted regions in rice mutants. Deletions ranged in size from one gene model to similar to 500 kb and were predicted on all 12 rice chromosomes. The utility of the technique as a tool in forward genetics was demonstrated in combination with an allelic series of mutants to rapidly narrow the genomic region, and eventually identify a candidate gene responsible for a lesion mimic phenotype. Finally, the positions of mutations in 14 mutants were aligned onto the rice pseudomolecules in a user-friendly genome browser to allow for rapid identification of untagged mutations http://irfgc.irri.org/cgi-bin/gbrowse/IR64_deletion_mutants/. Conclusion: We demonstrate the utility of oligonucleotide arrays to discover deleted genes in rice. The density and distribution of deletions suggests the feasibility of a database saturated with deletions across the rice genome. This community resource can continue to grow with further hybridizations, allowing researchers to quickly identify mutants that harbor deletions in candidate genomic regions, for example, regions containing QTL of interest.
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页数:11
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