Evidence map›Paper›PMID 12139012›Full record

ArticlePlant molecular biology2002

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

Surabhi Raina, Ramamurthy Mahalingam, Fuqiang Chen, Nina Fedoroff

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Article in Plant molecular biology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. A barley activation tagging system.Plant molecular biology · 2007
    Article
  9. Article
  10. Article
  11. Review
  12. Mapping Ds insertions in barley using a sequence-based approach.Molecular genetics and genomics : MGG · 2004
    Article
  13. Article
  14. Article
  15. Article
  16. Article
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Surabhi RainaLife Sciences Consortium and Biotechnology Institute, Pennsylvania State University, University Park 16802, USA.
Ramamurthy Mahalingam
Fuqiang Chen
Nina Fedoroff

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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 Arabidopsis chromosomes. 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 Arabidopsis genome 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 Arabidopsis lines 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.

Indexed as

ArabidopsisBinding SitesChromosome MappingDNA, PlantDNA Transposable ElementsGenome, PlantMutagenesis, InsertionalOpen Reading FramesPlants, Genetically ModifiedSequence Analysis, DNADNA, PlantDNA Transposable ElementsNon-programmatic

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.