Front. Mol. Biosci. Frontiers in Molecular Biosciences Front. Mol. Biosci. 2296-889X Frontiers Media S.A. 819157 10.3389/fmolb.2021.819157 Molecular Biosciences Correction Corrigendum: Identification and Characterization of Thermostable Y-Family DNA Polymerases η, ι, κ and Rev1 From a Lower Eukaryote, Thermomyces lanuginosus Vaisman et al. Corrigendum: Thermomyces lanuginosus Y-Family DNA Polymerases Vaisman Alexandra 1 † § McDonald John P. 1 † § Smith Mallory R. 1 † Aspelund Sender L. 1 † ‡ Evans Thomas C. Jr 2 † Woodgate Roger 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 New England Biolabs Incorporated, Ipswich, MA, United States

Approved by: Frontiers Editorial Office, Frontiers Media SA, Switzerland

 *Correspondence: Roger Woodgate, woodgate@nih.gov

These authors share first authorship

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

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

 15 12 2021 2021 8 819157 20 11 2021 22 11 2021 Copyright © 2021 Vaisman, McDonald, Smith, Aspelund, Evans and Woodgate. 2021 Vaisman, McDonald, Smith, Aspelund, Evans and Woodgate

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 A Corrigendum on Identification and Characterization of Thermostable Y-Family DNA Polymerases η, ι, κ and Rev1 From a Lower Eukaryote, Thermomyces lanuginosus by Vaisman A, McDonald JP, Smith MR, Aspelund SL, Evans TC and Woodgate R (2021). Front. Mol. Biosci. 8:778400. doi: 10.3389/fmolb.2021.778400 thermostable fungi Y-family DNA polymerases phylogenetic analysis translesion DNA synthesis DNA polymerase η DNA polymerase ι DNA polymerase κ REV1

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.

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​ A TT​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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