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      Dynamic Basis for dG•dT misincorporation via tautomerization and ionization

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          Abstract

          Tautomeric and anionic Watson-Crick-like mismatches play important roles in replication and translation errors through mechanisms that are not fully understood. Using NMR relaxation dispersion, we resolved a sequence-dependent kinetic network connecting G•T/U wobbles with three distinct Watson-Crick mismatches consisting of two rapidly exchanging tautomeric species (G enol•T/U⇌G•T enol/U enol; population <0.4%) and one anionic species (G•T /U ; population ≈0.001% at neutral pH). Inserting the sequence-dependent tautomerization/ionization step into a minimal kinetic mechanism for correct incorporation during replication following initial nucleotide binding leads to accurate predictions of dG•dT misincorporation probability across different polymerases, pH conditions, and for a chemically modified nucleotide, and provides mechanisms for sequence-dependent misincorporation. Our results indicate that the energetic penalty for tautomerization/ionization accounts for ≈10 −2−10 −3–fold discrimination against misincorporation, which proceeds primarily via tautomeric dG enol•dT and dG•dT enol with contributions from anionic dG•dT dominating at pH ≥8.4 or for some mutagenic nucleotides.

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          Most cited references51

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          Stem cell divisions, somatic mutations, cancer etiology, and cancer prevention

          Cancers are caused by mutations that may be inherited, induced by environmental factors, or result from DNA replication errors (R). We studied the relationship between the number of normal stem cell divisions and the risk of 17 cancer types in 69 countries throughout the world. The data revealed a strong correlation (median = 0.80) between cancer incidence and normal stem cell divisions in all countries, regardless of their environment. The major role of R mutations in cancer etiology was supported by an independent approach, based solely on cancer genome sequencing and epidemiological data, which suggested that R mutations are responsible for two-thirds of the mutations in human cancers. All of these results are consistent with epidemiological estimates of the fraction of cancers that can be prevented by changes in the environment. Moreover, they accentuate the importance of early detection and intervention to reduce deaths from the many cancers arising from unavoidable R mutations.
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            Structural basis of the translational elongation cycle.

            The sequential addition of amino acids to a growing polypeptide chain is carried out by the ribosome in a complicated multistep process called the elongation cycle. It involves accurate selection of each aminoacyl tRNA as dictated by the mRNA codon, catalysis of peptide bond formation, and movement of the tRNAs and mRNA through the ribosome. The process requires the GTPase factors elongation factor Tu (EF-Tu) and EF-G. Not surprisingly, large conformational changes in both the ribosome and its tRNA substrates occur throughout protein elongation. Major advances in our understanding of the elongation cycle have been made in the past few years as a result of high-resolution crystal structures that capture various states of the process, as well as biochemical and computational studies.
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              THE STRUCTURE OF DNA

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                Author and article information

                Journal
                0410462
                6011
                Nature
                Nature
                Nature
                0028-0836
                1476-4687
                1 February 2018
                31 January 2018
                08 February 2018
                31 July 2018
                : 554
                : 7691
                : 195-201
                Affiliations
                [1 ]Department of Biochemistry, Duke University Medical Center, Durham, North Carolina 27710, USA
                [2 ]Department of Chemistry and Biochemistry, The Ohio State University, Columbus, OH 43210, USA
                [3 ]The Ohio State Biochemistry Program, The Ohio State University, Columbus, OH 43210, USA
                [4 ]Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, USA
                [5 ]Department of Chemistry, Duke University, Durham, North Carolina 27710, USA
                Author notes
                Correspondence and requests for materials should be addressed to Z.S. ( suo.3@ 123456osu.edu ) or H.M.A. ( hashim.al.hashimi@ 123456duke.edu )
                [*]

                These authors contributed equally to this work.

                [†]

                Present Address: Nymirum, Durham, North Carolina 27713, USA

                [@]

                Present Address: Institute of Basic Science, Center for Soft and Living Matter, Ulsan, South Korea

                [+]

                Present Address: School of Life Sciences, Tsinghua University, Beijing, China

                [#]

                Present Address: Department of Chemistry, Indian Institute of Science Education and Research Bhopal, Bhopal 462 066, India

                Article
                NIHMS932197
                10.1038/nature25487
                5808992
                29420478
                32b75b75-0351-4f47-aa76-9c952e2903a2

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