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Hypothesis: transcript-templated repair of DNA double-strand breaks

机译:假设:DNA双链断裂的转录本模板修复

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Two mechanisms are available for the repair of DNA double-strand breaks (DSBs) in eukaryotic cells: homology directed repair (HDR) and non-homologous endjoining (NHEJ). While NHEJ is not restricted to a particular phase of the cell cycle, it is incapable of accurately repairing DBSs that have suffered a loss or gain of nucleotide sequence information. In contrast, HDR achieves accurate repair of such DSBs by use of a sister chromatid as a DNA template, but is restricted to cell cycle phases (S/GZ) when such templates are available. In this scheme, G, cells appear to lack a mechanism for the accurate repair of certain DSBs, and an ability to use alternative templates would be highly advantageous. Considered here, therefore, is the possibility that RNA transcripts are used as templates for HDR. Potential mechanisms for transcript-templated HDR, and ways in which it might be detected, are presented.
机译:有两种机制可用于修复真核细胞中的DNA双链断裂(DSB):同源性定向修复(HDR)和非同源末端连接(NHEJ)。虽然NHEJ不限于细胞周期的特定阶段,但它无法准确修复遭受核苷酸序列信息丢失或获得的DBS。相反,HDR通过使用姐妹染色单体作为DNA模板实现了此类DSB的准确修复,但在此类模板可用时,仅限于细胞周期阶段(S / GZ)。在这种方案中,G细胞似乎缺乏精确修复某些DSB的机制,使用替代模板的能力将非常有利。因此,这里考虑将RNA转录本用作HDR模板的可能性。介绍了转录模板HDR的潜在机制,以及检测它的方式。

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