Efficient Identification of Arabidopsis Knock-Out Mutants Using DNA-Arrays of Transposon Flanking Sequences

Abstract

Mutants obtained by insertional mutagenesis are widely used for determining gene-phenotype relationships. In Arabidopsis thaliana, several populations mutagenized either by T-DNA or transposon insertion are available for screening for knockout mutants in genes of interest. We have so far screened our Arabidopsis population mutagenized with the Zea mays transposon En-1/Spm for insertion mutations in 718 genes, using PCR on DNA pools. Although successful, this common approach is too time consuming for use in systematic screening of all 25 498 predicted genes of the Arabidopsis genome. We therefore investigated the use of DNA arrays for the direct identification of mutants in our population. All transposon-flanking regions from individual plants are amplified by PCR and subsequently spotted at high density onto nylon membranes. A single hybridization experiment with a gene-specific probe then allows one to identify candidate mutant plants. The efficiency of each separate step was determined and optimized. Screening of filters representing 2880 plants for insertions in 144 genes and subsequent investigation of some of the potential insertion mutants suggest that an overall screening efficiency of 50 % is attained.

Key words

Arabidopsis - transposon tagging - DNA arrays - reverse genetics - functional genomics

References

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Section Editor: F. Salamini