Abstract
In a companion study, a number of P element insertions into the singed locus were characterized. Here is reported a detailed analysis of the structure and mutability of another P element insertion at sn, known as sn(cm). Under conditions which mobilize P elements, sn(cm) mutates at high frequency to both wild-type (sn(+)) and to a much more extreme allele (sn(ext)). Wild-type revertants appear to represent precise or nearly precise excisions of the P element. Certainly two, and most likely all five, of the sn(ext) alleles studied result from the insertion of a duplicate copy of this P element into a nearby site in an inverted orientation. We propose a model in which both the sn(+) and sn(ext) mutational events can be explained by excision of the P element from one chromatid followed by reintegration into the sister chromatid at a nearby site (intracistronic transposition). Finally, it is shown that the sn(ext) alleles are themselves unstable and the structure of a resulting chromosome aberration is examined.
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Selected References
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