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假设:DNA双链断裂的转录本模板修复

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

作者信息

Trott Deborah A, Porter Andrew C G

机构信息

Division of Investigative Science, Department of Haematology, Imperial College Faculty of Medicine, London, UK.

出版信息

Bioessays. 2006 Jan;28(1):78-83. doi: 10.1002/bies.20339.

Abstract

Two mechanisms are available for the repair of DNA double-strand breaks (DSBs) in eukaryotic cells: homology directed repair (HDR) and non-homologous end-joining (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/G2) when such templates are available. In this scheme, G1 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.

摘要

真核细胞中存在两种修复DNA双链断裂(DSB)的机制:同源定向修复(HDR)和非同源末端连接(NHEJ)。虽然NHEJ不受细胞周期特定阶段的限制,但它无法准确修复核苷酸序列信息发生缺失或增加的双链断裂。相比之下,HDR通过使用姐妹染色单体作为DNA模板来实现此类双链断裂的精确修复,但仅限于有此类模板的细胞周期阶段(S/G2)。在这种情况下,G1期细胞似乎缺乏精确修复某些双链断裂的机制,而使用替代模板的能力将非常有利。因此,这里考虑的是RNA转录本用作HDR模板的可能性。本文介绍了转录本模板化HDR的潜在机制及其可能的检测方法。

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