Xu X, Hsia A P, Zhang L, Nikolau B J, Schnable P S
Department of Zoology and Genetics, Iowa State University, Ames 50011, USA.
Plant Cell. 1995 Dec;7(12):2151-61. doi: 10.1105/tpc.7.12.2151.
Sequence analysis of recombination break points has defined a 377-bp recombination hot spot within the anthocyanin 1 (a1) gene. One-fifth of all recombination events that occurred within the 140-kb a1-shrunken 2 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 a1 recombination hot spot is located within the 5' transcribed region of the a1 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 Mutator 1 transposon insertion in the a1-mum2 allele does not alter the sites at which recombination events resolve.
重组断点的序列分析确定了花青素1(a1)基因内一个377bp的重组热点。在140kb的a1-皱缩2区间内发生的所有重组事件中,有五分之一在这个377bp的热点内解析。在酵母中,染色体DNA的减数分裂双链断裂被认为启动重组,并且通常位于编码区的5'端,靠近转录启动子序列。由于a1重组热点位于a1基因的5'转录区内,重组事件起始和解析的位点似乎不同,但两者似乎都与转录序列相关且受到调控。虽然已知转座子插入会抑制重组并改变交叉与表观基因转换的比例,但a1-mum2等位基因中的Mutator 1转座子插入不会改变重组事件解析的位点。