Simplified Transposon Display (STD): a New Procedure for Isolation of a Gene Tagged by a Transposable Element Belonging to the Tpn1 Family in the Japanese Morning Glory.
- 1 January 2001
- journal article
- Published by Japanese Society for Plant Cell and Molecular Biology in Plant Biotechnology
- Vol. 18 (2) , 143-149
- https://doi.org/10.5511/plantbiotechnology.18.143
Abstract
Transposable elements are regarded as a powerful mutagen and as an effective tool to isolate genes tagged by transposon insertions. In the Japanese morning glory, a number of spontaneous mutants related to the colors and shapes of the flowers have been isolated. The plant contains around 500-1000 copies of an En/Spm-related element Tpn1 and its relatives, which act as major spontaneous mutagens. We have developed a new protocol for identifying genes tagged by insertion of Tpn1-related elements. The procedure, named simplified transposon display (STD), is simple and requires neither biotinylated oligonucleotides nor streptavidin-capturing which are essential in other transposon display methods published recently. Here we describe the details of STD used for identification of the Purple(Pr) gene that encodes a vacuolar Na+/H+ exchanger for increasing vacuolar pH responsible for blue flower coloration.Keywords
This publication has 14 references indexed in Scilit:
- Colour-enhancing protein in blue petalsNature, 2000
- Molecular cloning and expression of the Na+/H+ exchanger gene in Oryza sativaBiochimica et Biophysica Acta (BBA) - Gene Structure and Expression, 1999
- Floricultural Traits and Transposable Elements in the Japanese and Common Morning GloriesaaAnnals of the New York Academy of Sciences, 1999
- Plant tagnologyTrends in Plant Science, 1999
- The Arabidopsis thaliana proton transporters, AtNhx1 and Avp1, can function in cation detoxification in yeastProceedings of the National Academy of Sciences, 1999
- Molecular characterization of the mutableflakedallele for flower variegation in the common morning gloryThe Plant Journal, 1998
- A general method for gene isolation in tagging approaches: amplification of insertion mutagenised sites (AIMS)The Plant Journal, 1998
- Amplified Restriction Fragment Length Polymorphism-Based mRNA Fingerprinting Using a Single Restriction Enzyme That Recognizes a 4-bp SequenceBiochemical and Biophysical Research Communications, 1997
- Identification of New Chalcone Synthase Genes for Flower Pigmentation in the Japanese and Common Morning GloriesPlant and Cell Physiology, 1997
- Isolation of a Suppressor-mutator/Enhancer-like transposable element, Tpn1, from Japanese morning glory bearing variegated flowers.Plant Cell, 1994