Evidence map›Paper›PMID 41959459›Full record

ArticlebioRxiv : the preprint server for biology2026

Module-Selection Balance in the Evolution of Modular Organisms.

Mark Kim, Sarah M Ardell, Sergey Kryazhimskiy

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Mark KimDepartment of Ecology, Behavior and Evolution, University of California San Diego, La Jolla, CA 92093.
Sarah M ArdellDepartment of Ecology, Behavior and Evolution, University of California San Diego, La Jolla, CA 92093.
Sergey KryazhimskiyDepartment of Ecology, Behavior and Evolution, University of California San Diego, La Jolla, CA 92093.ORCID 0000-0001-9128-8705

Funding

Pathways in Biological Sciences Training ProgramT32GM133351 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Matthew Daugherty, Randolph Y. Hampton · 2020 to 2026
$9.9M
Characterizing variation in the local structure of fitness landscapes to assess the predictability of evolutionR01GM137112 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KRYAZHIMSKIY, SERGEY A. · 2020 to 2023
$1.2M
Empirical and Theoretical Studies of Adaptive Mutations in Microbes and Their Evolutionary ConsequencesR35GM153242 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Sergey A. Kryazhimskiy · 2024 to 2026
$1.2M
NIGMS NIH HHS R01 GM137112NIGMS NIH HHS R35 GM153242NIGMS NIH HHS T32 GM133351
6 · The paper itself

Abstract

The architecture of the genotype-phenotype-fitness map (GPFM) is a key determinant of evolutionary dynamics. One salient feature of biological GPFMs is variational modularity, where each mutation affects only a small subset of functional traits. Variational modularity may constrain the dynamics of trait evolution, but these constraints are not well understood. Here, we use several extensions of the Fisher's geometric model with two functional traits to investigate these constrains. We find that on GPFMs with universal pleiotropy, populations evolve along the fitness gradient, which implies that the trait under stronger selection is optimized exponentially faster than the trait under weaker selection. In contrast, on modular GPFMs, populations approach a quasi-steady state that we term a "module-selection balance" where both traits improve at the same rate and their ratio remains constant. We demonstrate that the existence of a module-selection balance is robust with respect to the details of evolutionary dynamics and GPFMs themselves, as long as they are variationally modular. Our theory predicts that variationally modular organisms should exhibit stereotypical bi-phasic dynamics of genome evolution, especially in the strong clonal interference regime, and we find support for this prediction in metagenomic data from Lenski's long-term evolution experiment in bacterium

Identifiers

PMID41959459
PMCPMC13060315

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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.