Abstract
About this talk
Lincosamide antibiotics inhibit the regeneration of plants in tissue culture. Resistance to lincosamides can be conferred by a mutation that modifies the ribosomal target site in the plastid genome, or by a transgene that encodes detoxification activity. We exploited both mechanisms to recover lincosamide-tolerant events in tissue culture. We identified several lincosamide nucleotidyltransferase (lnu) genes from medical studies and modified them for expression in plants. Four of these genes, the lnuAN2s, lnuBs, lnuDs and lnuFs function as highly efficient selectable markers for nuclear transformation of multiple dicot species. Under lincosamide pressure, we recovered transgenic tobacco, potato and Arabidopsis events with similar transformation frequencies as reported with kanamycin selection using the nptII gene. In the absence of a transgene, lincosamide tolerant lines developed in tobacco tissue culture over several weeks. Analysis of the plastid rrn23 sequence of these events revealed point mutations or 1nt insertions at the putative lincosamide binding site. The efficiency of the lnu marker genes makes them useful additions to the toolkit of plant biologists. Furthermore, our ability to select for a plastid trait using lincosamide antibiotics sets the stage for the development of lnu genes as plastid markers in genotypes with increased antibiotic susceptibility.
Take Away Notes:
• My presentation will describe the discovery and development of highly efficient selectable marker genes for plant transformation.
• Other researchers are welcome to make use of these genes in their own research, and my presentation will highlight how to maximize their potential
• This work will be put in the larger context of our work towards maize chloroplast transformation. There will be a molecular component about our development of the expression signals driving these genes.
Speaker
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