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考虑基于同源性的蚊子 DNA 修复:序列异质性和供体模板来源的影响。

Considerations for homology-based DNA repair in mosquitoes: Impact of sequence heterology and donor template source.

机构信息

The Pirbright Institute, Pirbright, Woking, United Kingdom.

Mathematical Ecology Research Group, Department of Zoology, University of Oxford, Oxford, United Kingdom.

出版信息

PLoS Genet. 2022 Feb 18;18(2):e1010060. doi: 10.1371/journal.pgen.1010060. eCollection 2022 Feb.

Abstract

The increasing prevalence of insecticide resistance and the ongoing global burden of vector-borne diseases have encouraged new efforts in mosquito control. For Aedes aegypti, the most important arboviral vector, integration rates achieved in Cas9-based knock-ins so far have been rather low, highlighting the need to understand gene conversion patterns and other factors that influence homology-directed repair (HDR) events in this species. In this study, we report the effects of sequence mismatches or donor template forms on integration rates. We found that modest sequence differences between construct homology arms [DNA sequence in the donor template which resembles the region flanking the target cut] and genomic target comprising 1.2% nucleotide dissimilarity (heterology) significantly reduced integration rates. While most integrations (59-88%) from plasmid templates were the result of canonical [on target, perfect repair] HDR events, no canonical events were identified from other donor types (i.e. ssDNA, biotinylated ds/ssDNA). Sequencing of the transgene flanking region in 69 individuals with canonical integrations revealed 60% of conversion tracts to be unidirectional and extend up to 220 bp proximal to the break, though in three individuals bidirectional conversion of up to 725 bp was observed.

摘要

杀虫剂抗性的不断增加和持续存在的全球虫媒传染病负担促使人们加大了蚊虫控制的力度。对于埃及伊蚊(最重要的虫媒病毒载体之一)来说,基于 Cas9 的基因敲入中达到的整合率相当低,这凸显了了解基因转换模式和影响同源定向修复(HDR)事件的其他因素的必要性。在这项研究中,我们报告了序列错配或供体模板形式对整合率的影响。我们发现,构建同源臂[供体模板中的 DNA 序列,类似于目标切割区域侧翼的区域]与基因组靶标之间的适度序列差异(1.2%的核苷酸差异,即异源性)显著降低了整合率。虽然大多数来自质粒模板的整合(59-88%)是典型的[靶标上,完美修复]HDR 事件的结果,但从其他供体类型(即 ssDNA、生物素化 ds/ssDNA)中未鉴定出典型事件。对 69 个具有典型整合的转基因侧翼区域进行测序,发现 60%的转换轨迹是单向的,延伸到断裂点近端 220 bp 处,但在 3 个人中观察到长达 725 bp 的双向转换。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c0b/8893643/75fb65b875f8/pgen.1010060.g001.jpg

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