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FIDELITY MECHANISMS IN DNA REPLICATION
Abstract
BASE INSERTION SELECTIVITY BY DNA POL YMERASES . The Base 1''lSertion Pathway . Structural Aspects to Base Selection by DNA Polymerases . Polymerase Insertion Errors . Fidelity Assays and Major Conclusions . Error Avoidance in Base Insertion----General Conclusions ..... .
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“The geometries of A⅐T and G⅐C base pairs are remarkably similar to each other but differ from mismatched base pairs (15,19,24,31,32).”
From DNA Replication Fidelity (2004) · cites this paper as [31]
In the citing paper
“This tight fit is consistent with a concept that emerged about 25 years ago (reviewed in Refs.15 and 31) that nucleotide selectivity largely depends on geometric selection for the shape and size of correct Watson-Crick base pairs.”
From DNA Replication Fidelity (2004) · cites this paper as [31]
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“In general, three discrete steps to ensure fidelity have been identified (7, 11).”
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“Among the various cellular proofreading elements including the genes responsible for base selection, exonucleolytic editing, MMR (Methyl-directed Mismatch Repair), and DNA repair [15-18], we chose the dnaQ gene which encodes the ε subunit of E.”
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“Such sequence-specific variation is not surprising, having been observed as well with proteinaceous polymerases (Echols and Goodman 1991; Kunkel 1992).”
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“DNA Pols with 39-59 exonuclease deficiencies exhibit elevated spontaneous mutation frequencies, thereby verifying that these synthesis and repair activities can regulate the production of mutations in vivo (10, 13, 27, 28, 38).”
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Self-citationMutT‐related error avoidance mechanism for DNA synthesis
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“Studies with Escherichia coli have revealed that products of genes with mutations which cause distinct mutator phenotypes are involved in each of these steps (Horiuchi et al. 1989; Modrich 1991; Echols & Goodman 1991 ).”
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“also seen, a phenomenon observed with proteinaceous polymerases ( 16 , 17).”
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“However, according to data obtained for various eukaryotic cells, this bypass is often mutagenic (Echols and Goodman 1991; Lis et al. 2008; Sabouri et al. 2008).”
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“Replicative DNA polymerases cannot insert nucleotides opposite damaged sites on template DNA due to their high fidelity and stringency of nucleotide incorporation, and replication is stalled ( Echols & Goodman 1991 ).”
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“that maintain the fidelity of the process by a base selection mechanism and a 3′-5′exonuclease activity able to proofread DNA polymerization errors (Echols and Goodman 1991; Hwang et al. 2004), yielding mutation rates usually in the range from 10–10 to 10–9 (Drake 1991).”
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“…dNTP is comprised of polymerase residues making interactions with the DNA minor groove edge, van der Waals interactions with the sugar and base, and electrostatic interactions with the triphosphate moiety of the incoming nucleotide (Echols and Goodman, 1991; Kool et al., 2000; Goodman, 1997).”
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Background
Metadata
- Authors
- Echols, H., & Goodman, M. F.
- Affiliations
- University of California, Berkeley (US)
- ORCID
- Goodman, Myron F.
- Venue
- Annual Review of Biochemistry
- Publisher
- Annual Reviews
- Published
- 1991-06
- Volume
- 60
- Issue
- 1
- Pages
- 477-511
- ISSN
- 0066-4154 (ISSN-L)
- 1545-4509
- OpenAlex
- W2138476183
- Cited by
- 712
- References
- 0
- Citations by year
- 2026: 3 · 2025: 7 · 2024: 11 · 2023: 4 · 2022: 8 · 2021: 3 · 2020: 7 · 2019: 9 · 2018: 9 · 2017: 15 · 2016: 9 · 2015: 12 · 2014: 16 · 2013: 20 · 2012: 18
- FWCI
- 12.30
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annual Review of Biochemistry (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Francis Crick Institute
- Vlaamse regering
- National Institutes of Health (5r01ca041655-10, 5r01gm042554-13)
- National Cancer Institute (CA 41655)
- National Institute of General Medical Sciences (GM 42554, GM 21422)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA and Nucleic Acid Chemistry
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Keywords
- DNA replication fidelity, DNA polymerase, insertion errors, polymerase structure, error prevention
- MeSH terms
- DNA Damage, DNA-Directed DNA Polymerase, DNA Replication, Escherichia coli, Kinetics, Mutation, SOS Response, Genetics
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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