18
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Insertional tagging, cloning, and expression of the Toxoplasma gondii hypoxanthine-xanthine-guanine phosphoribosyltransferase gene. Use as a selectable marker for stable transformation.

      The Journal of Biological Chemistry

      pharmacology, Amino Acid Sequence, Animals, Animals, Genetically Modified, Base Sequence, Biological Markers, Cloning, Molecular, DNA Primers, Drug Resistance, Gene Expression, Genes, Protozoan, Humans, Hypoxanthine Phosphoribosyltransferase, biosynthesis, chemistry, genetics, Kinetics, Mice, Molecular Sequence Data, Mutagenesis, Insertional, Phylogeny, Polymerase Chain Reaction, Recombinant Proteins, metabolism, Restriction Mapping, Sequence Deletion, Sequence Homology, Amino Acid, Sequence Homology, Nucleic Acid, Toxoplasma, drug effects, enzymology, Transformation, Genetic, Xanthines

      Read this article at

      ScienceOpenPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          A nonhomologous integration vector was used to identify the Toxoplasma gondii hypoxanthine-xanthine-guanine phosphoribosyl transferase (HXGPRT) gene by insertional mutagenesis. Parasite mutants resistant to 6-thioxanthine arose at a frequency of approximately3 x 10(-7). Genomic DNA flanking the insertion sites was retrieved by marker rescue and used to identify molecular clones exhibiting unambiguous homology to H(X)GPRT genes from other species. Sequence analysis of vector/genome junction sites reveals that integration of the linearized vector occurred with minimal rearrangement of either vector or target sequences, although the addition of filler DNA and small duplications or deletions of genomic sequences at the transgene termini was observed. Two differentially spliced classes of cDNA clones were identified, both of which complement hpt and gpt mutations in Escherichia coli. Kinetic analysis of purified recombinant enzyme revealed no significant differences between the two isoforms. Internally deleted clones spanning the genomic locus were used to create "knock-out" parasites, which lack all detectable HXGPRT activity. Complete activity could be restored to these knock-out mutants by transient transformation with either genomic DNA or cDNA-derived minigenes encoding both enzyme isoforms. Stable HXGPRT+ transformants were isolated under selection with mycophenolic acid, demonstrating the feasibility of HXGPRT as both a positive and negative selectable marker for stable transformation of T. gondii.

          Related collections

          Author and article information

          Journal
          8662859

          Comments

          Comment on this article