Foulis Steven J, Fowler Kyle R, Steiner Walter W
Department of Biology, Niagara University, Box 2032, Lewiston, NY, 14109, USA.
Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY, 14214, USA.
Genetica. 2018 Feb;146(1):65-74. doi: 10.1007/s10709-017-9997-3. Epub 2017 Oct 25.
Homologous recombination occurs at a greatly elevated frequency in meiosis compared to mitosis and is initiated by programmed double-strand DNA breaks (DSBs). DSBs do not occur at uniform frequency throughout the genome in most organisms, but occur preferentially at a limited number of sites referred to as hotspots. The location of hotspots have been determined at nucleotide-level resolution in both the budding and fission yeasts, and while several patterns have emerged regarding preferred locations for DSB hotspots, it remains unclear why particular sites experience DSBs at much higher frequency than other sites with seemingly similar properties. Short sequence motifs, which are often sites for binding of transcription factors, are known to be responsible for a number of hotspots. In this study we identified the minimum sequence required for activity of one of such motif identified in a screen of random sequences capable of producing recombination hotspots. The experimentally determined sequence, GGTCTRGACC, closely matches the previously inferred sequence. Full hotspot activity requires an effective sequence length of 9.5 bp, whereas moderate activity requires an effective sequence length of approximately 8.2 bp and shows significant association with DSB hotspots. In combination with our previous work, this result is consistent with a large number of different sequence motifs capable of producing recombination hotspots, and supports a model in which hotspots can be rapidly regenerated by mutation as they are lost through recombination.
与有丝分裂相比,同源重组在减数分裂中的发生频率大大提高,并且由程序性双链DNA断裂(DSB)引发。在大多数生物体中,DSB并非在整个基因组中以均匀的频率发生,而是优先发生在有限数量的被称为热点的位点。在芽殖酵母和裂殖酵母中,热点的位置已在核苷酸水平分辨率上确定,虽然关于DSB热点的优先位置已经出现了几种模式,但仍不清楚为什么特定位点经历DSB的频率比其他具有看似相似特性的位点高得多。短序列基序通常是转录因子结合的位点,已知它们是许多热点的原因。在这项研究中,我们确定了在能够产生重组热点的随机序列筛选中鉴定出的此类基序之一的活性所需的最小序列。实验确定的序列GGTCTRGACC与先前推断的序列紧密匹配。完整的热点活性需要9.5 bp的有效序列长度,而中等活性需要约8.2 bp的有效序列长度,并且与DSB热点显示出显著关联。结合我们之前的工作,这一结果与大量能够产生重组热点的不同序列基序一致,并支持一个模型,即热点在通过重组丢失时可以通过突变迅速再生。