Evidence map›Paper›PMID 27739533›Full record

ReviewNature reviews. Genetics2016

Genetic drift, selection and the evolution of the mutation rate.

Michael Lynch, Matthew S Ackerman, Jean-Francois Gout, Hongan Long, Way Sung, W Kelley Thomas, Patricia L Foster

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 471 papers.

0numbers the graph read from it
0cells of the map it votes in
471citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

471 citing papers in PubMed.

  1. Article
  2. Article
  3. Dynamics of mutators of arbitrary dominance in humans.bioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Article
  6. AScience advances · 2026
    Article
  7. Article
  8. Article
  9. Nucleotide diversity is a poor predictor of short-term adaptive potential.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  10. Article
  11. Article
  12. Effect of methylation on genome mutability in cattle.Genetics, selection, evolution : GSE · 2026
    Article
  13. Article
  14. Evolution of the highest fidelity DNA replication systems.bioRxiv : the preprint server for biology · 2026
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

411 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Michael LynchDepartment of Biology, Indiana University, Bloomington, Indiana 47401, USA.
Matthew S AckermanDepartment of Biology, Indiana University, Bloomington, Indiana 47401, USA.
Jean-Francois GoutDepartment of Biology, Indiana University, Bloomington, Indiana 47401, USA.
Hongan LongDepartment of Biology, Indiana University, Bloomington, Indiana 47401, USA.
Way SungDepartment of Biology, Indiana University, Bloomington, Indiana 47401, USA.
W Kelley ThomasDepartment of Molecular, Cellular, and Biomedical Sciences, University of New Hampshire, Durham, New Hampshire 03824, USA.
Patricia L FosterDepartment of Biology, Indiana University, Bloomington, Indiana 47401, USA.

Funding

The Rate and Molecular Spectrum of Spontaneous MutationsR01GM036827 · NIGMS · UNIVERSITY OF OREGON · PI LYNCH, MICHAEL R · 1988 to 2016
$5.7M
Population Genomics of Daphnia pulexR01GM101672 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI LYNCH, MICHAEL R · 2013 to 2016
$2.3M
NIGMS NIH HHS R01 GM036827NIGMS NIH HHS R01 GM101672
6 · The paper itself

Abstract

As one of the few cellular traits that can be quantified across the tree of life, DNA-replication fidelity provides an excellent platform for understanding fundamental evolutionary processes. Furthermore, because mutation is the ultimate source of all genetic variation, clarifying why mutation rates vary is crucial for understanding all areas of biology. A potentially revealing hypothesis for mutation-rate evolution is that natural selection primarily operates to improve replication fidelity, with the ultimate limits to what can be achieved set by the power of random genetic drift. This drift-barrier hypothesis is consistent with comparative measures of mutation rates, provides a simple explanation for the existence of error-prone polymerases and yields a formal counter-argument to the view that selection fine-tunes gene-specific mutation rates.

Indexed as

Biological EvolutionGenetic DriftMutation RateGenetic VariationHumansModels, GeneticSelection, Genetic

Identifiers

PMID27739533

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.