Evidence map›Paper›PMID 42184164›Full record

ArticleCell reports2026

Convergent evolution through independent rearrangements in the primate amylase locus.

Charikleia Karageorgiou, Petar Pajic, Stefan Ruhl, Omer Gokcumen

Abstract read
In one paragraph

Article in Cell reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Charikleia KarageorgiouDepartment of Biological Sciences, University at Buffalo, Buffalo, NY 14260, USA.
Petar PajicDepartment of Chemistry, Yale University, New Haven, CT 06511, USA.
Stefan RuhlDepartment of Oral Biology, School of Dental Medicine, University at Buffalo, Buffalo, NY 14214, USA.
Omer GokcumenDepartment of Biological Sciences, University at Buffalo, Buffalo, NY 14260, USA. Electronic address: omergokc@buffalo.edu.

Funding

Evolutionary and functional impact of common genomic structural variationsR35GM156519 · NIGMS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI Omer Gokcumen · 2025 to 2026
$887k
NIGMS NIH HHS R35 GM156519
6 · The paper itself

Abstract

Structurally complex genomic regions can foster evolutionary convergence by repeatedly generating gene duplications that yield similar expression patterns and traits across lineages. Focusing on the primate amylase locus, we leveraged high-quality genome assemblies from 53 primate species and multi-tissue transcriptomes from Old World monkeys to reconstruct the evolutionary history of recurrent duplications. We show that lineage-specific long terminal repeat retrotransposon insertions may be associated with initial structural instability, while subsequent duplications are primarily driven by non-allelic homologous recombination. Independent duplications in rhesus macaques, olive baboons, and great apes produced distinct amylase copies with convergent expression in pancreas and salivary glands, and it signals episodic diversifying selection, consistent with emerging functional divergence. Our analyses indicate that an ancestral gene with dual pancreas and salivary expression in Catarrhini duplicated in great apes, facilitating subfunctionalization and regulatory rewiring. These findings illuminate how modular structural and regulatory variation drives evolutionary innovation and molecular convergence.

Indexed as

AmylasesEvolution, MolecularGene RearrangementGenetic LociPrimatesAnimalsGene DuplicationHumansPhylogenyAmylasesamylase locusconvergent evolutionCP: molecular biologygene duplicationNAHRnon-allelic homologous recombinationrecurrent duplicationstructural variationsubfunctionalizationtissue-specific gene expressiontransposable elements

Identifiers

PMID42184164
PMCPMC13374492

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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.