Abstract
The commonly studied Caenorhabditis elegans strain Bristol N2 contains approximately 15 copies per genome of the transposon Tc3. However, Tc3 is not active in Bristol N2. Tc3 contains one major open reading frame (Tc3A). We have fused this open reading frame to an inducible promoter and expressed it in a transgenic Bristol N2 line. Tc3A expression resulted in frequent excision and transposition of endogenous Tc3 elements. This shows that the Bristol N2 genome contains Tc3 transposons that are cis proficient for transposition, but are immobile because Tc3A is absent. We demonstrate that recombinant Tc3A binds specifically to the terminal nucleotides of the Tc3 inverted repeat, indicating that Tc3A is the Tc3 transposase. Activation of Tc3 transposition in vivo was accompanied by the appearance of extrachromosomal, linear copies of Tc3. These may be intermediates in Tc3 transposition.
MeSH Terms
Animals
Base Sequence
Binding Sites
Caenorhabditis elegans/enzymology,genetics
Chromosomes
Cloning, Molecular
DNA/metabolism
DNA Transposable Elements
Gene Expression
Larva/growth & development
Molecular Sequence Data
Nucleotidyltransferases/metabolism
Repetitive Sequences, Nucleic Acid
Transposases
Chemicals
DNA Transposable Elements
DNA
Nucleotidyltransferases
Transposases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
van Luenen H G
Netherlands Cancer Institute, Division of Molecular Biology, Amsterdam.
Colloms S D
Plasterk R H
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