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内源序列模式影响拟南芥中CRISPR/Cas9诱导的DNA双链断裂的修复模式。

Endogenous sequence patterns predispose the repair modes of CRISPR/Cas9-induced DNA double-stranded breaks in Arabidopsis thaliana.

作者信息

Vu Giang T H, Cao Hieu X, Fauser Friedrich, Reiss Bernd, Puchta Holger, Schubert Ingo

机构信息

Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), D 06466, Gatersleben, Stadt Seeland, Germany.

Botanical Institute II, Karlsruhe Institute of Technology, POB 6980, Karlsruhe, 76049, Germany.

出版信息

Plant J. 2017 Oct;92(1):57-67. doi: 10.1111/tpj.13634. Epub 2017 Aug 14.

Abstract

The possibility to predict the outcome of targeted DNA double-stranded break (DSB) repair would be desirable for genome editing. Furthermore the consequences of mis-repair of potentially cell-lethal DSBs and the underlying pathways are not yet fully understood. Here we study the clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9-induced mutation spectra at three selected endogenous loci in Arabidopsis thaliana by deep sequencing of long amplicon libraries. Notably, we found sequence-dependent genomic features that affected the DNA repair outcome. Deletions of 1-bp to <1000-bp size and/or very short insertions, deletions >1 kbp (all due to NHEJ) and deletions combined with insertions between 5-bp to >100 bp [caused by a synthesis-dependent strand annealing (SDSA)-like mechanism] occurred most frequently at all three loci. The appearance of single-stranded annealing events depends on the presence and distance between repeats flanking the DSB. The frequency and size of insertions is increased if a sequence with high similarity to the target site was available in cis. Most deletions were linked to pre-existing microhomology. Deletion and/or insertion mutations were blunt-end ligated or via de novo generated microhomology. While most mutation types and, to some degree, their predictability are comparable with animal systems, the broad range of deletion mutations seems to be a peculiar feature of the plant A. thaliana.

摘要

对于基因组编辑而言,预测靶向DNA双链断裂(DSB)修复结果的可能性是非常可取的。此外,潜在的细胞致死性DSB错配修复的后果及其潜在途径尚未完全了解。在这里,我们通过对长扩增子文库进行深度测序,研究了拟南芥中三个选定内源性位点的成簇规律间隔短回文重复序列(CRISPR)/Cas9诱导的突变谱。值得注意的是,我们发现了影响DNA修复结果的序列依赖性基因组特征。1bp至<1000bp大小的缺失和/或非常短的插入、>1kbp的缺失(均由非同源末端连接所致)以及5bp至>100bp之间的缺失与插入组合(由类合成依赖链退火(SDSA)机制引起)在所有三个位点最为常见。单链退火事件的出现取决于DSB侧翼重复序列的存在及其间距。如果顺式中存在与靶位点高度相似的序列,则插入的频率和大小会增加。大多数缺失与预先存在的微同源性有关。缺失和/或插入突变通过平端连接或通过从头产生的微同源性产生。虽然大多数突变类型及其在某种程度上的可预测性与动物系统相当,但广泛的缺失突变似乎是植物拟南芥的一个独特特征。

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