DSBCapture: in situ capture and sequencing of DNA breaks.

DSBCapture: in situ capture and sequencing of DNA breaks.
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DOI:
10.1038/nmeth.3960
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发表时间:
2016-10
期刊:
影响因子:
48
通讯作者:
Balasubramanian, Shankar
Balasubramanian, Shankar
中科院分区:
生物学1区
文献类型:
--
作者:
Lensing, Stefanie V.;Marsico, Giovanni;Hansel-Hertsch, Robert;Lam, Enid Y.;Tannahill, David;Balasubramanian, Shankar

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双链DNA断裂(DSBs)不断出现并引起突变和染色体重排。在这里,我们提出了DSBCapture,这是一种基于测序的方法,可以捕获DSBsin位点,并在单核苷酸分辨率下直接绘制这些位点,从而能够研究DSB的起源。与其他方法相比,DSBCapture的灵敏度和数据产出率显著提高。利用DSBCapture,我们发现了dsb与核小体缺失染色质中转录升高之间的惊人关系。
Double-strand DNA breaks (DSBs) continuously arise and cause mutations and chromosomal rearrangements. Here, we present DSBCapture, a sequencing-based method that captures DSBsin situand directly maps these at single-nucleotide resolution, enabling the study of DSB origin. DSBCapture shows substantially increased sensitivity and data yield compared with other methods. Using DSBCapture, we uncovered a striking relationship between DSBs and elevated transcription within nucleosome-depleted chromatin.
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