Evidence map›Paper›PMID 30598529›Full record

ArticleNature ecology & evolution2019

The dynamics of adaptive genetic diversity during the early stages of clonal evolution.

Jamie R Blundell, Katja Schwartz, Danielle Francois, Daniel S Fisher, Gavin Sherlock, Sasha F Levy

Abstract read
In one paragraph

Article in Nature ecology & evolution, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Ecological diversification in rapidly evolving populations.bioRxiv : the preprint server for biology · 2025
    Article
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  11. Review
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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

6 authors.

Jamie R BlundellDepartment of Applied Physics, Stanford University, Stanford, CA, USA. jrb75@cam.ac.uk.
Katja SchwartzDepartment of Genetics, Stanford University, Stanford, CA, USA.
Danielle FrancoisLaufer Center for Physical and Quantitative Biology, Stony Brook University, Stony Brook, NY, USA.
Daniel S FisherDepartment of Applied Physics, Stanford University, Stanford, CA, USA.
Gavin SherlockDepartment of Genetics, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-1692-4983
Sasha F LevyLaufer Center for Physical and Quantitative Biology, Stony Brook University, Stony Brook, NY, USA. sflevy@stanford.edu.ORCID http://orcid.org/0000-0002-0923-1636

Funding

Molecular Characterization of Adaptive EvolutionR01HG003328 · NHGRI · STANFORD UNIVERSITY · PI SHERLOCK, GAVIN J · 2005 to 2015
$4.1M
Systematic Molecular Analysis of Antagonistic PleiotropyR01GM110275 · NIGMS · STANFORD UNIVERSITY · PI SHERLOCK, GAVIN J · 2014 to 2017
$1.6M
PPiSeq: High-Throughput Protein-Protein Interaction SequencingR01HG008354 · NHGRI · STATE UNIVERSITY NEW YORK STONY BROOK · PI LEVY, SASHA F · 2015 to 2018
$1.5M
NHGRI NIH HHS R01 HG003328NHGRI NIH HHS R01 HG008354NIGMS NIH HHS R01 GM110275
6 · The paper itself

Abstract

The dynamics of genetic diversity in large clonally evolving cell populations are poorly understood, despite having implications for the treatment of cancer and microbial infections. Here, we combine barcode lineage tracking, sequencing of adaptive clones and mathematical modelling of mutational dynamics to understand adaptive diversity changes during experimental evolution of Saccharomyces cerevisiae under nitrogen and carbon limitation. We find that, despite differences in beneficial mutational mechanisms and fitness effects, early adaptive genetic diversity increases predictably, driven by the expansion of many single-mutant lineages. However, a crash in adaptive diversity follows, caused by highly fit double-mutant 'jackpot' clones that are fed from exponentially growing single mutants, a process closely related to the classic Luria-Delbrück experiment. The diversity crash is likely to be a general feature of asexual evolution with clonal interference; however, both its timing and magnitude are stochastic and depend on the population size, the distribution of beneficial fitness effects and patterns of epistasis.

Indexed as

Adaptation, BiologicalClonal EvolutionGenetic VariationModels, GeneticMutationSaccharomyces cerevisiae

Identifiers

PMID30598529
PMCPMC6517070

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.