Gene activation in plastids by the CRE site-specific recombinase

Tarinee Tungsuchat, Hiroshi Kuroda, Jarunya Narangajavana, Pal Maliga

Research output: Contribution to journalArticle

26 Citations (Scopus)

Abstract

We developed a novel system for gene activation in plastids that uses the CRE/loxP site-specific recombination system to create a translatable reading frame by excision of a blocking sequence. To test the system, we introduced an inactive gfp* gene into the tobacco plastid genome downstream of the selectable spectinomcyin resistance (aadA) marker gene. The aadA gene is the blocking sequence, and is flanked by directly oriented loxP sites for excision by the CRE. In the non-activated state, gfp* is transcribed from the aadA promoter, but the mRNA is not translated due to the lack of an AUG translation initiation codon. Green Fluorescent Protein (GFP) expression is activated by excision of the aadA coding segment to link up the gfp* coding region with the translation initiation codon of aadA. Tobacco plants that carry the inactive gfp* gene do not contain detectable levels of GFP. However, activation of gfp* resulted in GFP accumulation, proving the utility of CRE-induced protein expression in tobacco chloroplasts. The gene activation system described here will be useful to probe plastid gene function and for the production of recombinant proteins in chloroplasts.

Original languageEnglish
Pages (from-to)711-718
Number of pages8
JournalPlant Molecular Biology
Volume61
Issue number4-5
DOIs
Publication statusPublished - Jul 2006
Externally publishedYes

    Fingerprint

Keywords

  • CRE/loxP site-specific recombination
  • Green fluorescent protein (GFP)
  • Nicotiana tabacum
  • Plastid gene activation
  • Plastid transformation

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Biochemistry

Cite this