P-element transposase is the enzyme encoded by an autonomous P element that supplies the catalytic machinery for its movement within DNA. The mobile element is a DNA sequence; its transposase is a protein. An engineered non-autonomous transposable element can retain the DNA features needed for recognition while depending on a separate transposase source.[ref]
A 1986 study linked candidate proteins to activity rather than relying only on a predicted coding sequence. Immunochemical methods identified an approximately polypeptide associated with a transcript lacking the third intron, and a roughly product associated with retention of that intron. Cells producing the larger polypeptide catalyzed precise and imprecise excision of a non-autonomous transposable element. The combined expression and activity evidence supported identification of the larger protein as P-element transposase.[ref]
Identification and immunochemical analysis of biologically active Drosophila P element transposase by D. C. Rio and others. Abstract, transcript processing, immunochemical detection and excision assay
A conceptual two-component comparison explains the genetic tool. One component carries the DNA to be moved; another supplies the transposase. Losing the enzyme-producing component can remove the machinery for further movement without necessarily removing a previously integrated cargo. This is a statement about separating recognition sequences from a diffusible protein, not a claim that every insertion is automatically stable under every genetic condition.
The result also illustrates why transcript structure matters. A gene can be present and expressed yet fail to produce the same active protein if its RNA splicing differs. For P-element transposase, the evidence connects the molecular form of the transcript to the size of the protein and then to a measurable DNA-rearrangement activity.
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