| Literature DB >> 32025478 |
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Abstract
[This corrects the article DOI: 10.1002/2211-5463.12380.].Entities:
Year: 2020 PMID: 32025478 PMCID: PMC6996387 DOI: 10.1002/2211-5463.12776
Source DB: PubMed Journal: FEBS Open Bio ISSN: 2211-5463 Impact factor: 2.792
Figure 1DNA repair efficiency in PAXX, XLF and XRCC4 HAP1 cells. (A) NHEJ‐deficient HAP1 cells were produced by Horizon Discovery. Two PAXX lines carry either 1‐bp insertion or 2‐bp deletion in exon 4. XRCC4 line carries 8‐bp deletion in exon 2. Two XLF lines carry either 10‐bp or 4‐bp deletion in exon 3. (B, C, D) WB assay detected no PAXX protein in PAXX and PAXX DNA‐PKcs cells (B), no XRCC4 in XRCC4 cells (C) and no XLF in XLF cells (D). (E) Proliferation of HAP1 cells of indicated genotypes. We present summary of three experiments; data from two PAXX and two XLF lines were pooled. Error bars are SD. (F, G) Sensitivity of HAP1 cells of indicated genotypes to double‐strand break‐inducing agents zeocin (F) and etoposide (G). Numbers represent count of colonies normalized to mock‐treated controls. Four experiments were performed. Data from two PAXX and two XLF lines were pooled. Error bars are SD. (H) Genomic instability in HAP1 cells of indicated genotypes. Count of chromosomal breaks and chromatid breaks; average breaks per cell are shown for reference.