Sequence analysis of recombination break points has defined a 377-bp recombination hot spot within the anthocyanin1 (al) gene. One-fifth of all recombination events that occurred within the 140-kb a1-shrunken2 interval resolved within this 377-bp hot spot. In yeast, meiotic double-strand breaks in chromosomal DNA are thought to initiate recombination and are generally located 5' of coding regions, near transcription promoter sequences. Because the al recombination hot spot is located within the 5' transcribed region of the al gene, the sites at which recombination events initiate and resolve appear to be different, but both appear to be regulated in relation to transcribed sequences, Although transposon insertions are known to suppress recombination and alter the ratio of crossovers to apparent gene conversions, the Mutator1 transposon insertion in the a1-mum2 allele does not alter the sites at which recombination events resolve.