Wu T C, Lichten M
Laboratory of Biochemistry, National Cancer Institute, Bethesda, Maryland 20892, USA.
Genetics. 1995 May;140(1):55-66. doi: 10.1093/genetics/140.1.55.
Double-strand DNA breaks (DSBs) initiate meiotic recombination in Saccharomyces cerevisiae. DSBs occur at sites that are hypersensitive in nuclease digests of chromatin, suggesting a role for chromatin structure in determining DSB location. We show here that the frequency of DSBs at a site is not determined simply by DNA sequence or by features of chromatin structure. An arg4-containing plasmid was inserted at several different locations in the yeast genome. Meiosis-induced DSBs occurred at similar sites in pBR322-derived portions of the construct at all insert loci, and the frequency of these breaks varied in a manner that mirrored the frequency of meiotic recombination in the arg4 portion of the insert. However, DSBs did not occur in the insert-borne arg4 gene at a site that is frequently broken at the normal ARG4 locus, even though the insert-borne arg4 gene and the normal ARG4 locus displayed similar DNase I hypersensitivity patterns. Deletions that removed active DSB sites from an insert at HIS4 restored breaks to the insert-borne arg4 gene and to a DSB site in flanking chromosomal sequences. We conclude that the frequency of DSB at a site can be affected by sequences several thousand nucleotides away and suggest that this is because of competition between DSB sites for locally limited factors.
双链DNA断裂(DSBs)引发酿酒酵母中的减数分裂重组。DSBs发生在染色质核酸酶消化中高度敏感的位点,这表明染色质结构在确定DSB位置中起作用。我们在此表明,一个位点处DSBs的频率并非简单地由DNA序列或染色质结构特征所决定。一个含arg4的质粒被插入到酵母基因组的几个不同位置。减数分裂诱导的DSBs在构建体中源自pBR322的部分的相似位点处发生于所有插入位点,并且这些断裂的频率以反映插入片段中arg4部分减数分裂重组频率的方式变化。然而,插入片段携带的arg4基因中在正常ARG4位点经常发生断裂的位点并未出现DSBs,尽管插入片段携带的arg4基因和正常ARG4位点显示出相似的DNase I超敏反应模式。从HIS4处的一个插入片段中去除活性DSB位点的缺失将断裂恢复到插入片段携带的arg4基因以及侧翼染色体序列中的一个DSB位点。我们得出结论,一个位点处DSB的频率可能受到数千个核苷酸以外的序列的影响,并表明这是由于DSB位点之间对局部有限因子的竞争所致。