<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang Y</submitter><funding>National Institute of Environmental Health Sciences</funding><funding>NIEHS NIH HHS</funding><pagination>695-698</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7965357</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>34(3)</volume><pubmed_abstract>Alkylation represents a main form of DNA damage. The &lt;i>N&lt;/i>&lt;sup>2&lt;/sup> position of guanine is frequently alkylated in DNA. The SOS-induced polymerases have been shown to be capable of bypassing various DNA damage products in &lt;i>Escherichia coli&lt;/i>. Herein, we explored the influences of four &lt;i>N&lt;/i>&lt;sup>2&lt;/sup>-alkyl-dG lesions (alkyl = ethyl, &lt;i>n&lt;/i>-butyl, isobutyl, or &lt;i>sec&lt;/i>-butyl) on DNA replication in AB1157 &lt;i>E. coli&lt;/i> cells and the corresponding strains with polymerases (Pol) II, IV, and V being individually or simultaneously knocked out. We found that &lt;i>N&lt;/i>&lt;sup>2&lt;/sup>-Et-dG is slightly less blocking to DNA replication than the &lt;i>N&lt;/i>&lt;sup>2&lt;/sup>-Bu-dG lesions, which display very similar replication bypass efficiencies. Additionally, Pol II and, to a lesser degree,</pubmed_abstract><journal>Chemical research in toxicology</journal><pubmed_title>DNA Polymerase II Supports the Replicative Bypass of &lt;i>N&lt;/i>&lt;sup>2&lt;/sup>-Alkyl-2'-deoxyguanosine Lesions in &lt;i>Escherichia coli&lt;/i> Cells.</pubmed_title><pmcid>PMC7965357</pmcid><funding_grant_id>R35 ES031707</funding_grant_id><pubmed_authors>Wu J</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>DNA Polymerase II Supports the Replicative Bypass of &lt;i>N&lt;/i>&lt;sup>2&lt;/sup>-Alkyl-2'-deoxyguanosine Lesions in &lt;i>Escherichia coli&lt;/i> Cells.</name><description>Alkylation represents a main form of DNA damage. The &lt;i>N&lt;/i>&lt;sup>2&lt;/sup> position of guanine is frequently alkylated in DNA. The SOS-induced polymerases have been shown to be capable of bypassing various DNA damage products in &lt;i>Escherichia coli&lt;/i>. Herein, we explored the influences of four &lt;i>N&lt;/i>&lt;sup>2&lt;/sup>-alkyl-dG lesions (alkyl = ethyl, &lt;i>n&lt;/i>-butyl, isobutyl, or &lt;i>sec&lt;/i>-butyl) on DNA replication in AB1157 &lt;i>E. coli&lt;/i> cells and the corresponding strains with polymerases (Pol) II, IV, and V being individually or simultaneously knocked out. We found that &lt;i>N&lt;/i>&lt;sup>2&lt;/sup>-Et-dG is slightly less blocking to DNA replication than the &lt;i>N&lt;/i>&lt;sup>2&lt;/sup>-Bu-dG lesions, which display very similar replication bypass efficiencies. Additionally, Pol II and, to a lesser degree,</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2025-04-18T15:11:05.502Z</modification><creation>2025-02-18T23:35:40.279Z</creation></dates><accession>S-EPMC7965357</accession><cross_references><pubmed>33417436</pubmed><doi>10.1021/acs.chemrestox.0c00478</doi></cross_references></HashMap>