Molecular analysis of rice plants harboring a multi-functional T-DNA tagging system

J Genet Genomics. 2009 May;36(5):267-76. doi: 10.1016/S1673-8527(08)60114-9.

Abstract

About 25,000 rice T-DNA insertional mutant lines were generated using the vector pCAS04 which has both promoter-trapping and activation-tagging function. Southern blot analysis revealed that about 40% of these mutants were single copy integration and the average T-DNA insertion number was 2.28. By extensive phenotyping in the field, quite a number of agronomically important mutants were obtained. Histochemical GUS assay with 4,310 primary mutants revealed that the GUS-staining frequency was higher than that of the previous reports in various tissues and especially high in flowers. The T-DNA flanking sequences of some mutants were isolated and the T-DNA insertion sites were mapped to the rice genome. The flanking sequence analysis demonstrated the different integration pattern of the right border and left border into rice genome. Compared with Arabidopsis and poplar, it is much varied in the T-DNA border junctions in rice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosomes, Plant / genetics
  • DNA, Bacterial / genetics*
  • Genes, Reporter
  • Genetic Vectors / genetics
  • Genome, Plant
  • Glucuronidase / genetics
  • Glucuronidase / metabolism
  • Mutagenesis, Insertional*
  • Oryza / genetics*
  • Oryza / growth & development
  • Oryza / metabolism
  • Rhizobium / genetics
  • Rhizobium / metabolism
  • Transformation, Genetic

Substances

  • DNA, Bacterial
  • T-DNA
  • Glucuronidase