APOBEC3A/B-induced mutagenesis is responsible for 20% of heritable mutations in the TpCpW context
Published 2016 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
APOBEC3A/B-induced mutagenesis is responsible for 20% of heritable mutations in the TpCpW context
Authors
Keywords
-
Journal
GENOME RESEARCH
Volume 27, Issue 2, Pages 175-184
Publisher
Cold Spring Harbor Laboratory
Online
2016-12-10
DOI
10.1101/gr.210336.116
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Mutational Strand Asymmetries in Cancer Genomes Reveal Mechanisms of DNA Damage and Repair
- (2016) Nicholas J. Haradhvala et al. CELL
- APOBEC3A damages the cellular genome during DNA replication
- (2016) Abby M. Green et al. CELL CYCLE
- Clustered mutations in hominid genome evolution are consistent with APOBEC3G enzymatic activity
- (2016) Yishay Pinto et al. GENOME RESEARCH
- APOBEC-induced mutations in human cancers are strongly enriched on the lagging DNA strand during replication
- (2016) Vladimir B. Seplyarskiy et al. GENOME RESEARCH
- Landscape of somatic mutations in 560 breast cancer whole-genome sequences
- (2016) Serena Nik-Zainal et al. NATURE
- An expanded sequence context model broadly explains variability in polymorphism levels across the human genome
- (2016) Varun Aggarwala et al. NATURE GENETICS
- Parent-of-origin-specific signatures of de novo mutations
- (2016) Jakob M Goldmann et al. NATURE GENETICS
- Mutation Processes in 293-Based Clones Overexpressing the DNA Cytosine Deaminase APOBEC3B
- (2016) Monica K. Akre et al. PLoS One
- Strand-biased cytosine deamination at the replication fork causes cytosine to thymine mutations inEscherichia coli
- (2016) Ashok S. Bhagwat et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The DNA cytosine deaminase APOBEC3H haplotype I likely contributes to breast and lung cancer mutagenesis
- (2016) Gabriel J. Starrett et al. Nature Communications
- New observations on maternal age effect on germline de novo mutations
- (2016) Wendy S. W. Wong et al. Nature Communications
- The topography of mutational processes in breast cancer genomes
- (2016) Sandro Morganella et al. Nature Communications
- APOBEC3A and APOBEC3B Preferentially Deaminate the Lagging Strand Template during DNA Replication
- (2016) James I. Hoopes et al. Cell Reports
- Mutational History of a Human Cell Lineage from Somatic to Induced Pluripotent Stem Cells
- (2016) Foad J. Rouhani et al. PLoS Genetics
- Genome-wide characteristics of de novo mutations in autism
- (2016) Ryan KC Yuen et al. npj Genomic Medicine
- Concurrent Nucleotide Substitution Mutations in the Human Genome Are Characterized by a Significantly Decreased Transition/Transversion Ratio
- (2015) Wenjuan Zhu et al. HUMAN MUTATION
- DNA Editing of LTR Retrotransposons Reveals the Impact of APOBECs on Vertebrate Genomes
- (2015) Binyamin A. Knisbacher et al. MOLECULAR BIOLOGY AND EVOLUTION
- Polymerase ζ Activity Is Linked to Replication Timing in Humans: Evidence from Mutational Signatures
- (2015) Vladimir B. Seplyarskiy et al. MOLECULAR BIOLOGY AND EVOLUTION
- Parent–progeny sequencing indicates higher mutation rates in heterozygotes
- (2015) Sihai Yang et al. NATURE
- A global reference for human genetic variation
- (2015) Richard A. Gibbs et al. NATURE
- Genome-wide patterns and properties of de novo mutations in humans
- (2015) Laurent C Francioli et al. NATURE GENETICS
- An APOBEC3A hypermutation signature is distinguishable from the signature of background mutagenesis by APOBEC3B in human cancers
- (2015) Kin Chan et al. NATURE GENETICS
- Timing, rates and spectra of human germline mutation
- (2015) Raheleh Rahbari et al. NATURE GENETICS
- Crossovers are associated with mutation and biased gene conversion at recombination hotspots
- (2015) Barbara Arbeithuber et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Somatic mutation in cancer and normal cells
- (2015) I. Martincorena et al. SCIENCE
- The origins, determinants, and consequences of human mutations
- (2015) J. Shendure et al. SCIENCE
- DNA Polymerase ζ-Dependent Lesion Bypass in Saccharomyces cerevisiae Is Accompanied by Error-Prone Copying of Long Stretches of Adjacent DNA
- (2015) Olga V. Kochenova et al. PLoS Genetics
- Genetic Variation in Human DNA Replication Timing
- (2014) Amnon Koren et al. CELL
- Multiplatform Analysis of 12 Cancer Types Reveals Molecular Classification within and across Tissues of Origin
- (2014) Katherine A. Hoadley et al. CELL
- A double-edged sword: R loops as threats to genome integrity and powerful regulators of gene expression
- (2014) K. Skourti-Stathaki et al. GENES & DEVELOPMENT
- Heterogeneous polymerase fidelity and mismatch repair bias genome variation and composition
- (2014) Scott A. Lujan et al. GENOME RESEARCH
- Error-prone polymerase activity causes multinucleotide mutations in humans
- (2014) Kelley Harris et al. GENOME RESEARCH
- Mechanisms underlying mutational signatures in human cancers
- (2014) Thomas Helleday et al. NATURE REVIEWS GENETICS
- Recombination initiation maps of individual human genomes
- (2014) F. Pratto et al. SCIENCE
- Mutational Context and Diverse Clonal Development in Early and Late Bladder Cancer
- (2014) Iver Nordentoft et al. Cell Reports
- Demography and the Age of Rare Variants
- (2014) Iain Mathieson et al. PLoS Genetics
- Human APOBEC3 Induced Mutation of Human Immunodeficiency Virus Type-1 Contributes to Adaptation and Evolution in Natural Infection
- (2014) Eun-Young Kim et al. PLoS Pathogens
- Repair of naturally occurring mismatches can induce mutations in flanking DNA
- (2014) Jia Chen et al. eLife
- The choice of nucleotide inserted opposite abasic sites formed within chromosomal DNA reveals the polymerase activities participating in translesion DNA synthesis
- (2013) Kin Chan et al. DNA REPAIR
- The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes
- (2013) S. B. Montgomery et al. GENOME RESEARCH
- Prevalence of Multinucleotide Replacements in Evolution of Primates and Drosophila
- (2013) Nadezhda V. Terekhanova et al. MOLECULAR BIOLOGY AND EVOLUTION
- APOBEC3B is an enzymatic source of mutation in breast cancer
- (2013) Michael B. Burns et al. NATURE
- Mutational heterogeneity in cancer and the search for new cancer-associated genes
- (2013) Michael S. Lawrence et al. NATURE
- Signatures of mutational processes in human cancer
- (2013) Ludmil B. Alexandrov et al. NATURE
- Evidence for APOBEC3B mutagenesis in multiple human cancers
- (2013) Michael B Burns et al. NATURE GENETICS
- An APOBEC cytidine deaminase mutagenesis pattern is widespread in human cancers
- (2013) Steven A Roberts et al. NATURE GENETICS
- DNA deaminases induce break-associated mutation showers with implication of APOBEC3B and 3A in breast cancer kataegis
- (2013) Benjamin JM Taylor et al. eLife
- Mutational Processes Molding the Genomes of 21 Breast Cancers
- (2012) Serena Nik-Zainal et al. CELL
- Heterogeneity of the Transition/Transversion Ratio in Drosophila and Hominidae Genomes
- (2012) V. B. Seplyarskiy et al. MOLECULAR BIOLOGY AND EVOLUTION
- Rate of de novo mutations and the importance of father’s age to disease risk
- (2012) Augustine Kong et al. NATURE
- Replication Fork Polarity Gradients Revealed by Megabase-Sized U-Shaped Replication Timing Domains in Human Cell Lines
- (2012) Antoine Baker et al. PLoS Computational Biology
- Mismatch Repair Balances Leading and Lagging Strand DNA Replication Fidelity
- (2012) Scott A. Lujan et al. PLoS Genetics
- Pervasive Multinucleotide Mutational Events in Eukaryotes
- (2011) Daniel R. Schrider et al. CURRENT BIOLOGY
- Mutation Rate Distribution Inferred from Coincident SNPs and Coincident Substitutions
- (2011) Philip L. F. Johnson et al. Genome Biology and Evolution
- Replication-Associated Mutational Asymmetry in the Human Genome
- (2011) Chun-Long Chen et al. MOLECULAR BIOLOGY AND EVOLUTION
- Analysis of genomic variation in non-coding elements using population-scale sequencing data from the 1000 Genomes Project
- (2011) Xinmeng Jasmine Mu et al. NUCLEIC ACIDS RESEARCH
- Evidence for Sequential and Increasing Activation of Replication Origins along Replication Timing Gradients in the Human Genome
- (2011) Guillaume Guilbaud et al. PLoS Computational Biology
- A comprehensive catalogue of somatic mutations from a human cancer genome
- (2009) Erin D. Pleasance et al. NATURE
- Cryptic Variation in the Human Mutation Rate
- (2009) Alan Hodgkinson et al. PLOS BIOLOGY
- Global organization of replication time zones of the mouse genome
- (2008) S. Farkash-Amar et al. GENOME RESEARCH
- Transcription induces strand-specific mutations at the 5' end of human genes
- (2008) P. Polak et al. GENOME RESEARCH
- Transcription-Induced Mutational Strand Bias and Its Effect on Substitution Rates in Human Genes
- (2008) C. F. Mugal et al. MOLECULAR BIOLOGY AND EVOLUTION
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started