A collection of sequenced and mapped Ds transposon insertion sites in Arabidopsis thaliana

被引:28
作者
Surabhi Raina
Ramamurthy Mahalingam
Fuqiang Chen
Nina Fedoroff
机构
[1] Life Sciences Consortium and Biotechnology Institute,
[2] Pennsylvania State University,undefined
[3] Sigma-Aldrich Chemical Company,undefined
关键词
(; ); (; mapping; searchable database; TAIL PCR; transposon insertion lines;
D O I
10.1023/A:1016099215667
中图分类号
学科分类号
摘要
Insertional mutagenesis is a powerful tool for generating knockout mutations that facilitate associating biological functions with as yet uncharacterized open reading frames (ORFs) identified by genomic sequencing or represented in EST databases. We have generated a collection of Dissociation(Ds) transposon lines with insertions on all 5 Arabidopsischromosomes. Here we report the insertion sites in 260 independent single-transposon lines, derived from four different Ds donor sites. We amplified and determined the genomic sequence flanking each transposon, then mapped its insertion site by identity of the flanking sequences to the corresponding sequence in the Arabidopsisgenome database. This constitutes the largest collection of sequence-mapped Ds insertion sites unbiased by selection against the donor site. Insertion site clusters have been identified around three of the four donor sites on chromosomes 1 and 5, as well as near the nucleolus organizers on chromosomes 2 and 4. The distribution of insertions between ORFs and intergenic sequences is roughly proportional to the ratio of genic to intergenic sequence. Within ORFs, insertions cluster near the translational start codon, although we have not detected insertion site selectivity at the nucleotide sequence level. A searchable database of insertion site sequences for the 260 transposon insertion sites is available at http://sgio2.biotec.psu.edu/sr. This and other collections of Arabidopsislines with sequence-identified transposon insertion sites are a valuable genetic resource for functional genomics studies because the transposon location is precisely known, the transposon can be remobilized to generate revertants, and the Ds insertion can be used to initiate further local mutagenesis.
引用
收藏
页码:91 / 108
页数:17
相关论文
共 357 条
  • [1] Altschul S.F.(1990)Basic local alignment search tool J. Mol. Biol. 215 403-410
  • [2] Gish W.(1997)Gapped BLAST and PSIBLAST: a new generation of protein database search programs Nucl. Acids Res. 25 3389-3402
  • [3] Miller W.(1999) mutants lacking the 43-and 54-kilodalton subunits of the chloroplast signal recognition particle have distinct phenotypes Plant Physiol. 121 61-70
  • [4] Lipman D.J.(1992)Insertional mutagenesis of the maize P gene by intragenic transposition of Genetics 131 199-209
  • [5] Altschul S.F.(1992)Development of an efficient two-element transposon tagging system in Mol. Gen. Genet. 233 449-461
  • [6] Madden T.L.(1993)Factors affecting the excision frequency of the maize transposable element Mol. Gen. Genet. 240 65-72
  • [7] Schaffer A.A.(1993) in Genetics 134 1221-1229
  • [8] Zhang J.(1996)Transposition pattern of the maize element Plant J. 10 613-623
  • [9] Zhang Z.(1998) in Meth. Mol. Biol. 82 259-266
  • [10] Miller W.(1996)Maturation-specific translational enhancement mediated by the 5'-UTR of a late pollen transcript Mol. Gen. Genet. 251 428-435