Literature DB >> 32025478

Corrigendum to: Robust DNA repair in PAXX-deficient mammalian cells.

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Abstract

[This corrects the article DOI: 10.1002/2211-5463.12380.].
© 2020 The Authors. Published by FEBS Press and John Wiley & Sons Ltd.

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


In Figure 1B of the paper by Dewan et al. 1, the western blot lanes were incorrectly labelled. From left to right, the lanes should have been labelled as WT, PAXX, DNA‐PKcs and PAXX. This does not affect the conclusions of this paper. The corrected version of Figure 1 and its legend are provided here:
Figure 1

DNA 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.

DNA 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.
  1 in total

1.  Robust DNA repair in PAXX-deficient mammalian cells.

Authors:  Alisa Dewan; Mengtan Xing; Marie Benner Lundbæk; Raquel Gago-Fuentes; Carole Beck; Per Arne Aas; Nina-Beate Liabakk; Siri Sæterstad; Khac Thanh Phong Chau; Bodil Merete Kavli; Valentyn Oksenych
Journal:  FEBS Open Bio       Date:  2018-02-07       Impact factor: 2.693

  1 in total

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