PEM-seq comprehensively quantifies DNA repair outcomes during gene-editing and DSB repair
The repair products of double-stranded DNA breaks (DSBs) are crucial for investigating the mechanism underlying DNA damage repair as well as evaluating the safety and efficiency of gene-editing; however, a comprehensively quantitative assay remains to be established. Here, we describe the step-by-st...
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Veröffentlicht in: | STAR protocols 2022-03, Vol.3 (1), p.101088-101088, Article 101088 |
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Sprache: | eng |
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Zusammenfassung: | The repair products of double-stranded DNA breaks (DSBs) are crucial for investigating the mechanism underlying DNA damage repair as well as evaluating the safety and efficiency of gene-editing; however, a comprehensively quantitative assay remains to be established. Here, we describe the step-by-step instructions of the primer extension-mediated sequencing (PEM-seq), followed by the framework of data processing and statistical analysis. PEM-seq presents a full spectrum of repair outcomes for both genome-editing-induced and endogenous DSBs in mouse and human cells.
For complete details on the use and execution of this profile, please refer to Gan et al. (2021), Yin et al. (2019), Liu et al. (2021a), and Zhang et al. (2021).
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•PEM-seq comprehensively quantifies DSB repair outcomes•PEM-seq evaluates the efficiency and safety of genome-editing tools•PEM-seq studies the impact of DNA damage response pathways on DSB repair•PEM-seq identifies endogenous DNA damage sites and DNA fragment integrations
The repair products of double-stranded DNA breaks (DSBs) are crucial for investigating the mechanism underlying DNA damage repair as well as evaluating the safety and efficiency of gene-editing; however, a comprehensively quantitative assay remains to be established. Here, we describe the step-by-step instructions of the primer extension-mediated sequencing (PEM-seq), followed by the framework of data processing and statistical analysis. PEM-seq presents a full spectrum of repair outcomes for both genome-editing-induced and endogenous DSBs in mouse and human cells. |
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ISSN: | 2666-1667 2666-1667 |
DOI: | 10.1016/j.xpro.2021.101088 |