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CORRECTION article

Front. Mol. Biosci., 15 December 2021

Sec. Structural Biology

Volume 8 - 2021 | https://doi.org/10.3389/fmolb.2021.819157

Corrigendum: Identification and Characterization of Thermostable Y-Family DNA Polymerases η, ι, κ and Rev1 From a Lower Eukaryote, Thermomyces lanuginosus

    AV

    Alexandra Vaisman 1† §

    JP

    John P. McDonald 1† §

    MR

    Mallory R. Smith 1

    SL

    Sender L. Aspelund 1† ‡

    TC

    Thomas C. Evans Jr 2

    RW

    Roger Woodgate 1† *

  • 1. Laboratory of Genomic Integrity, National Institute of Child Health and Human Development, National Institutes of Health, 9800 Medical Center Drive, Bethesda, MD, United States

  • 2. New England Biolabs Incorporated, Ipswich, MA, United States

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In the original article, there was a formatting issue in Figure 6 as published. This occurred when the image was converted from a PC generated pdf to an Apple Macintosh generated tif for publication. The corrected Figure 6 appears below.

FIGURE 6

FIGURE 6

TLS past trans-S-BPDE-dA by T. lanuginosus pols. The ability to bypass BPDE-dA was assayed for (A) polη in thepresence of 4 mM Mg2+, (B) polκ in the presence of 4 mM Mg2+, (C) polη in the presence of 4 mM Mn2+, (D) polκ in the presence of 4 mM Mn2+, (E) polι in the presence of 4 mM Mn2+, and (F) individual, or a mixture of various pols in 4 mM Mn2+. The substrate used in these assays was made by annealing of the 32P labeled primer 5′-CAC​TGC​AGA​CTC​TAA​A-3′ and either an undamaged or BPDE-containing template 5′- GCT​CGT​CAG​CAG​ATT​TAG​AGT​CTG​CAG​TG-3′, where the underlined bold A stands for the undamaged, or BPDE modified dA. Reactions contained 100 μM each of individual nucleotide (dC, dG, dA, and dT) or a mixture of all four dNTPs as indicated in the figure and were carried out at 37°C for 10 min. Concentrations of enzymes were 0.17 pM for polη, 0.32 pM for polκ, and 0.15 pM for polι. The sequence of the template immediately downstream of the primer (pr) is shown on the left-hand side of each gel pair. The star (*) indicates the position of the adduct.

The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

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Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Summary

Keywords

thermostable fungi, Y-family DNA polymerases, phylogenetic analysis, translesion DNA synthesis, DNA polymerase η, DNA polymerase ι, DNA polymerase κ, REV1

Citation

Vaisman A, McDonald JP, Smith MR, Aspelund SL, Evans TC Jr and Woodgate R (2021) Corrigendum: Identification and Characterization of Thermostable Y-Family DNA Polymerases η, ι, κ and Rev1 From a Lower Eukaryote, Thermomyces lanuginosus. Front. Mol. Biosci. 8:819157. doi: 10.3389/fmolb.2021.819157

Received

20 November 2021

Accepted

22 November 2021

Published

15 December 2021

Approved by

Frontiers Editorial Office, Frontiers Media SA, Switzerland

Volume

8 - 2021

Updates

Copyright

*Correspondence: Roger Woodgate,

§These authors share first authorship

‡ Present address: Sender L. Aspelund, Novavax, Inc., Gaithersburg, MD, United States

ORCID: Alexandra Vaisman orcid.org/0000-0002-2521-1467 John P. McDonald orcid.org/0000-0003-2482-148X Mallory R. Smith orcid.org/0000-0003-1450-7825 Sender L. Aspelund orcid.org/0000-0003-0726-4028 Thomas C. Evans Jr. orcid.org/0000-0001-5406-0146 Roger Woodgate orcid.org/0000-0002-2521-1467

This article was submitted to Structural Biology, a section of the journal Frontiers in Molecular Biosciences

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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