Present address: Plant Nutrition Laboratory, Institute of Agricultural and Nutritional Sciences (IAEW), Faculty of Life Sciences III, University of Halle-Wittenberg, 06099 Halle (Saale), Germany.
Getting the most out of publicly available T-DNA insertion lines
Article first published online: 4 JUL 2008
© 2008 The Authors. Journal compilation © 2008 Blackwell Publishing Ltd
The Plant Journal
Volume 56, Issue 4, pages 665–677, November 2008
How to Cite
Ülker, B., Peiter, E., Dixon, D. P., Moffat, C., Capper, R., Bouché, N., Edwards, R., Sanders, D., Knight, H. and Knight, M. R. (2008), Getting the most out of publicly available T-DNA insertion lines. The Plant Journal, 56: 665–677. doi: 10.1111/j.1365-313X.2008.03608.x
- Issue published online: 11 NOV 2008
- Article first published online: 4 JUL 2008
- Received 23 April 2008; accepted 4 June 2008; published online 4 August 2008.
- activation tagging;
- intron splicing;
- 1′2′ promoter;
In the course of several different projects, we came to realize that there is a significant amount of untapped potential in the publicly available T-DNA insertion lines. In addition to the GABI-Kat lines, which were designed specifically for activation tagging, lines from the SAIL and FLAGdb collections are also useful for this purpose. As well as the 35S promoter chosen for activation tagging in GABI-Kat lines, we found that the 1′2′ bidirectional promoter is capable of activating expression of flanking genomic sequences in both GABI-Kat and SAIL lines. Thus these lines have added potential for activation tagging. We also show that these lines are capable of generating antisense transcripts and so have the potential to be used for suppression (loss/reduction of function) studies. By virtue of weak terminator sequences in some T-DNA constructs, transcript read-through from selectable markers is also possible, which again has the potential to be exploited in activation/suppression studies. Finally, we show that, by selecting and characterizing lines in which the T-DNA insertions are present specifically within introns of a target gene, an allelic series of mutants with varying levels of reduced expression can be generated, due to differences in efficiency of intron splicing. Taken together, our analyses demonstrate that there is a wealth of untapped potential within existing insertion lines for studies on gene function, and the effective exploitation of these resources is discussed.