A New Resource of Locally Transposed DissociationElements for Screening Gene-Knockout Lines in Silico on the Arabidopsis Genome1,212

We transposed Dissociation(Ds) elements from three start loci on chromosome 5 in Arabidopsis (Nossen ecotype) by using a local transposition system. We determined partial genomic sequences flanking the Dselements and mapped the elements' insertion sites in 1,173 transposed lines by comparison with the published genomic sequence. Most of the lines contained a single copy of the Ds element. One-half of the lines contained Ds on chromosome 5; in particular, insertion “hot spots” near the three start loci were clearly observed. In the other lines, the Ds elements were transposed across chromosomes. We found other insertion hot spots at the tops of chromosomes 2 and 4, near nucleolus organizer regions 2 and 4, respectively. Another characteristic feature was that theDs elements tended to transpose near the chromosome ends and rarely transposed near centromeres. The distribution patterns differed among the three start loci, even though they possessed the same Ds construct. More than one-half of theDs elements were inserted irregularly into the genome; that is, they did not retain the perfect inverted repeat sequence ofDs nor leave perfect target site duplications. This precise analysis of distribution patterns will contribute to a comprehensive understanding of the transposing mechanism. From theseDs insertion sites, we have constructed a database for screening gene-knockout mutants in silico. In 583 of the 1,173 lines, the Ds elements were inserted into protein-coding genes, which suggests that these lines are gene-knockout mutants. The database and individual lines will be available freely for academic use from the RIKEN Bio-Resource Center (http://www.brc.riken.go.jp/Eng/index.html).

[1]  V. Sundaresan,et al.  Analysis of Flanking Sequences from Dissociation Insertion Lines: A Database for Reverse Genetics in Arabidopsis , 1999, Plant Cell.

[2]  Yaoguang Liu,et al.  Thermal asymmetric interlaced PCR: automatable amplification and sequencing of insert end fragments from P1 and YAC clones for chromosome walking. , 1995, Genomics.

[3]  K. Shinozaki,et al.  Disruption of an Arabidopsis cytoplasmic ribosomal protein S13-homologous gene by transposon-mediated mutagenesis causes aberrant growth and development. , 2000, The Plant journal : for cell and molecular biology.

[4]  Taku Ito,et al.  RANDOM INSERTIONAL MUTAGENESIS IN ARABIDOPSIS , 2002 .

[5]  Maes,et al.  Plant tagnology. , 1999, Trends in plant science.

[6]  B. S. Ahloowalia,et al.  Molecular techniques in crop improvement , 2002 .

[7]  Jonathan D. G. Jones,et al.  Multiple Independent Defective Suppressor-mutator Transposon Insertions in Arabidopsis: A Tool for Functional Genomics , 1999, Plant Cell.

[8]  D. Shibata,et al.  Characterization and mapping of Ds-GUS-T-DNA lines for targeted insertional mutagenesis. , 1996, The Plant journal : for cell and molecular biology.

[9]  D. Shibata,et al.  Regional insertional mutagenesis of genes on Arabidopsis thaliana chromosome V using the Ac/Ds transposon in combination with a cDNA scanning method. , 1999, The Plant journal : for cell and molecular biology.

[10]  N. Fedoroff,et al.  A versatile system for detecting transposition in Arabidopsis. , 1993, The Plant journal : for cell and molecular biology.

[11]  K. Feldmann,et al.  T-DNA insertion mutagenesis in Arabidopsis: going back and forth. , 1997, Trends in genetics : TIG.

[12]  The Arabidopsis Genome Initiative Analysis of the genome sequence of the flowering plant Arabidopsis thaliana , 2000, Nature.

[13]  T. Ito,et al.  An essential role of a TatC homologue of a ΔpH- dependent protein transporter in thylakoid membrane formation during chloroplast development in Arabidopsis thaliana , 2001, Proceedings of the National Academy of Sciences of the United States of America.