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Figure 9.5 Targeted gene mutation in D. melanogaster is based on the gap repair hypothesis. If a P
element jumps out of a normal gene, it will leave a gap that must be repaired. Repair is thought to
involve using DNA with homologous ends from within the genome as a template for DNA repair.
If a new P element with a modified gene structure is present, the sequence in the gap can be filled
in using the modified gene as the template, leading to a targeted gene alteration. (Modified from
Gloor et al. 1991 .)
is sufficient to promote gap repair. However, gap repair was sensitive to single-
base mismatches within the homologous regions. Interestingly, the data sug-
gested that the ends of a broken chromosome could locate a single homologous
template anywhere in the genome using a short stretch of closely matching
sequence. How this occurs remains mysterious, but the search is sufficiently effi-
cient that up to several percent of the progeny exhibited targeted-gene replace-
ment at the white locus. This high rate of gene conversion is considered to be
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