<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>110(20)</volume><submitter>Zhao Y</submitter><funding>Intramural NIH HHS</funding><pubmed_abstract>Somatic hypermutation is programmed base substitutions in the variable regions of Ig genes for high-affinity antibody generation. Two motifs, RGYW and WA (R, purine; Y, pyrimidine; W, A or T), have been found to be somatic hypermutation hotspots. Overwhelming evidence suggests that DNA polymerase η (Pol η) is responsible for converting the WA motif to WG by misincorporating dGTP opposite the templating T. To elucidate the molecular mechanism, crystal structures and kinetics of human Pol η substituting dGTP for dATP in four sequence contexts, TA, AA, GA, and CA, have been determined and compared. The T:dGTP wobble base pair is stabilized by Gln-38 and Arg-61, two uniquely conserved residues among Pol η. Weak base paring of the W (T:A or A:T) at the primer end and their distinct interactions with Pol η lead to misincorporation of G in the WA motif. Between two WA motifs, our kinetic and structural data indicate that A-to-G mutation occurs more readily in the TA context than AA. Finally, Pol η can extend the T:G mispair efficiently to complete the mutagenesis.</pubmed_abstract><journal>Proceedings of the National Academy of Sciences of the United States of America</journal><pagination>8146-51</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3657764</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Mechanism of somatic hypermutation at the WA motif by human DNA polymerase η.</pubmed_title><pmcid>PMC3657764</pmcid><pubmed_authors>Yang W</pubmed_authors><pubmed_authors>Gregory MT</pubmed_authors><pubmed_authors>Hua YJ</pubmed_authors><pubmed_authors>Biertumpfel C</pubmed_authors><pubmed_authors>Hanaoka F</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mechanism of somatic hypermutation at the WA motif by human DNA polymerase η.</name><description>Somatic hypermutation is programmed base substitutions in the variable regions of Ig genes for high-affinity antibody generation. Two motifs, RGYW and WA (R, purine; Y, pyrimidine; W, A or T), have been found to be somatic hypermutation hotspots. Overwhelming evidence suggests that DNA polymerase η (Pol η) is responsible for converting the WA motif to WG by misincorporating dGTP opposite the templating T. To elucidate the molecular mechanism, crystal structures and kinetics of human Pol η substituting dGTP for dATP in four sequence contexts, TA, AA, GA, and CA, have been determined and compared. The T:dGTP wobble base pair is stabilized by Gln-38 and Arg-61, two uniquely conserved residues among Pol η. Weak base paring of the W (T:A or A:T) at the primer end and their distinct interactions with Pol η lead to misincorporation of G in the WA motif. Between two WA motifs, our kinetic and structural data indicate that A-to-G mutation occurs more readily in the TA context than AA. Finally, Pol η can extend the T:G mispair efficiently to complete the mutagenesis.</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013 May</publication><modification>2024-11-20T16:11:52.642Z</modification><creation>2019-03-27T01:10:08Z</creation></dates><accession>S-EPMC3657764</accession><cross_references><pubmed>23630267</pubmed><doi>10.1073/pnas.1303126110</doi></cross_references></HashMap>