Evidence map›Paper›PMID 36583227›Full record

ReviewGenome biology and evolution2023

Incompatibility and Interchangeability in Molecular Evolution.

Daniel B Sloan, Jessica M Warren, Alissa M Williams, Shady A Kuster, Evan S Forsythe

Abstract readReview
In one paragraph

Review in Genome biology and evolution, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Frontiers in veterinary science · 2025
    Article
  6. Article
  7. Photosynthetic demands on translational machinery drive retention of redundant tRNA metabolism in plant organelles.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. Genetic bias in repeated evolution of pigment loss in cave populations of the Asellus aquaticus species complex.Journal of experimental zoology. Part B, Molecular and developmental evolution · 2024
    Article
  9. Article
  10. Review
  11. Article
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

5 authors.

Daniel B SloanDepartment of Biology, Colorado State University, Fort Collins, Colorado.ORCID 0000-0002-3618-0897
Jessica M WarrenCenter for Mechanisms of Evolution, Biodesign Institute and School of Life Sciences, Arizona State University, Tempe, Arizona.ORCID 0000-0001-5263-0475
Alissa M WilliamsDepartment of Biological Sciences, Vanderbilt University, Nashville, Tennessee.ORCID 0000-0002-6840-2415
Shady A KusterDepartment of Biology, Colorado State University, Fort Collins, Colorado.
Evan S ForsytheDepartment of Biology, Colorado State University, Fort Collins, Colorado.ORCID 0000-0002-3865-2245

Funding

Predoctoral Training in Quantitative Cell & Molecular BiologyT32GM132057 · NIGMS · COLORADO STATE UNIVERSITY · PI Karen Marie Dobos, Brian Munsky · 2019 to 2026
$2.9M
Causes of Extreme Mitochondrial Mutation Rate VariationR01GM118046 · NIGMS · COLORADO STATE UNIVERSITY · PI SLOAN, DANIEL BENJAMIN · 2017 to 2021
$1.5M
Howard Hughes Medical InstituteNIGMS NIH HHS R01 GM118046NIGMS NIH HHS T32 GM132057
6 · The paper itself

Abstract

There is remarkable variation in the rate at which genetic incompatibilities in molecular interactions accumulate. In some cases, minor changes-even single-nucleotide substitutions-create major incompatibilities when hybridization forces new variants to function in a novel genetic background from an isolated population. In other cases, genes or even entire functional pathways can be horizontally transferred between anciently divergent evolutionary lineages that span the tree of life with little evidence of incompatibilities. In this review, we explore whether there are general principles that can explain why certain genes are prone to incompatibilities while others maintain interchangeability. We summarize evidence pointing to four genetic features that may contribute to greater resistance to functional replacement: (1) function in multisubunit enzyme complexes and protein-protein interactions, (2) sensitivity to changes in gene dosage, (3) rapid rate of sequence evolution, and (4) overall importance to cell viability, which creates sensitivity to small perturbations in molecular function. We discuss the relative levels of support for these different hypotheses and lay out future directions that may help explain the striking contrasts in patterns of incompatibility and interchangeability throughout the history of molecular evolution.

Indexed as

Evolution, MolecularHybridization, Geneticcytonuclearepistasishorizontal gene transferhybridizationprotein–protein interactions

Identifiers

PMID36583227
PMCPMC9839398

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.