Affiliations 

  • 1 Advanced Biotechnology and Breeding Centre, Malaysian Palm Oil Board Selangor, Malaysia
  • 2 School of Bioscience and Biotechnology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia Selangor, Malaysia ; Institute of System Biology (INBIOSIS), University Kebangsaan Malaysia Selangor, Malaysia
Front Plant Sci, 2015;6:727.
PMID: 26442041 DOI: 10.3389/fpls.2015.00727

Abstract

DOG(R)1, which encodes 2-deoxyglucose-6-phosphate phosphatase, has been used as a selectable marker gene to produce transgenic plants. In this study, a transformation vector, pBIDOG, which contains the DOG(R)1 gene, was transformed into oil palm embryogenic calli (EC) mediated by Agrobacterium tumefaciens strain LBA4404. Transformed EC were exposed to 400 mg l(-1) 2-deoxyglucose (2-DOG) as the selection agent. 2-DOG resistant tissues were regenerated into whole plantlets on various regeneration media containing the same concentration of 2-DOG. The plantlets were later transferred into soil and grown in a biosafety screenhouse. PCR and subsequently Southern blot analyses were carried out to confirm the integration of the transgene in the plantlets. A transformation efficiency of about 1.0% was obtained using DOG(R)1 gene into the genome of oil palm. This result demonstrates the potential of using combination of DOG(R)1 gene and 2-DOG for regenerating transgenic oil palm.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.