| Literature DB >> 2840332 |
R S Hawley1, R A Steuber, C H Marcus, R Sohn, D M Baronas, M L Cameron, A E Zitron, J W Chase.
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 sncm. Under conditions which mobilize P elements, sncm mutates at high frequency to both wild-type (sn+) and to a much more extreme allele (snext). Wild-type revertants appear to represent precise or nearly precise excisions of the P element. Certainly two, and most likely all five, of the snext 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 snext 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 snext alleles are themselves unstable and the structure of a resulting chromosome aberration is examined.Entities:
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Year: 1988 PMID: 2840332 PMCID: PMC1203348
Source DB: PubMed Journal: Genetics ISSN: 0016-6731 Impact factor: 4.562