Large-scale insertional mutagenesis using the Tnt1 retrotransposon in the model legume Medicago truncatula

• Published in: The Plant journal : for cell and molecular biology Vol. 54; no. 2; pp. 335 - 347
• Main Authors: Tadege, Million, Wen, Jiangqi, He, Ji, Tu, Haidi, Kwak, Younsig, Eschstruth, Alexis, Cayrel, Anne, Endre, Gabriella, Zhao, Patrick X, Chabaud, Mireille, Ratet, Pascal, Mysore, Kirankumar S
• Format: Journal Article
• Language: English
• Published: Oxford, UK Oxford, UK : Blackwell Publishing Ltd 01.04.2008; Blackwell Publishing Ltd; Blackwell Science
• Subjects: Biological and medical sciences; Botany; Diverse techniques; functional genomics; Fundamental and applied biological sciences. Psychology; Genes, Plant - genetics; Genomics; insertion mutagenesis; legume; Legumes; Medicago; Medicago truncatula; Medicago truncatula - genetics; Medicago truncatula - growth & development; Molecular and cellular biology; Mutagenesis, Insertional - methods; Mutation; Phenotype; Retroelements - genetics; retrotransposon; Tnt1 tagging; Medicago truncatula; Tnt1 tagging; Genomics; insertion mutagenesis; Tissue culture; Medicago; functional genomics; Leguminosae; Gene; legume; Dicotyledones; Angiospermae; Spermatophyta; Mutation; retrotransposon
• ISSN: 0960-7412; 1365-313X
• DOI: 10.1111/j.1365-313x.2008.03418.x

Medicago truncatula is a fast-emerging model for the study of legume functional biology. We used the tobacco retrotransposon Tnt1 to tag the Medicago genome and generated over 7600 independent lines representing an estimated 190 000 insertion events. Tnt1 inserted on average at 25 different locations per genome during tissue culture, and insertions were stable during subsequent generations in soil. Analysis of 2461 Tnt1 flanking sequence tags (FSTs) revealed that Tnt1 appears to prefer gene-rich regions. The proportion of Tnt1 insertion in coding sequences was 34.1%, compared to the expected 15.9% if random insertions were to occur. However, Tnt1 showed neither unique target site specificity nor strong insertion hot spots, although some genes were more frequently tagged than others. Forward-genetic screening of 3237 R₁ lines resulted in identification of visible mutant phenotypes in approximately 30% of the regenerated lines. Tagging efficiency appears to be high, as all of the 20 mutants examined so far were found to be tagged. Taking the properties of Tnt1 into account and assuming 1.7 kb for the average M. truncatula gene size, we estimate that approximately 14 000-16 000 lines would be sufficient for 90% gene tagging coverage in M. truncatula. This is in contrast to more than 500 000 lines required to achieve the same saturation level using T-DNA tagging. Our data demonstrate that Tnt1 is an efficient insertional mutagen in M. truncatula, and could be a primary choice for other plant species with large genomes.