High-throughput enhancer trap by remobilization of transposon Minos in Ciona intestinalis

Genesis. 2007 May;45(5):307-17. doi: 10.1002/dvg.20290.

Abstract

The enhancer trap approach utilizing transposons yields us information about gene functions and gene expression patterns. In the ascidian Ciona intestinalis, transposon-based transgenesis and insertional mutagenesis were achieved with a Tc1/mariner transposon Minos. We report development of a novel technique for enhancer trap in C. intestinalis. This technique uses remobilization of Minos in the Ciona genome. A Minos vector for enhancer trap was constructed and a tandem array insertion of the vector was introduced into the Ciona genome to create a mutator line. Minos was remobilized in Ciona chromosomes to create new insertions by providing transposases. These transposase-introduced animals were crossed with wild-type animals. Nearly 80% of F1 families showed novel GFP expression patterns. This high-throughput enhancer trap screen will be useful to create new marker transgenic lines showing reporter gene expression in specific tissues and to identify novel patterns of gene expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Base Sequence
  • Ciona intestinalis / genetics*
  • DNA / genetics
  • DNA Transposable Elements*
  • Enhancer Elements, Genetic*
  • Gene Expression
  • Genes, Reporter
  • Genetic Techniques
  • Genetic Vectors
  • Green Fluorescent Proteins / genetics
  • In Situ Hybridization, Fluorescence
  • Recombinant Proteins / genetics
  • Transposases / genetics

Substances

  • DNA Transposable Elements
  • Recombinant Proteins
  • Green Fluorescent Proteins
  • DNA
  • Minos transposase
  • Transposases