Evidence map›Paper›PMID 40446803›Full record

ArticleCell genomics2025

Disentangling cell-intrinsic and cell-extrinsic factors underlying evolution.

Alexander L Starr, Toshiya Nishimura, Kyomi J Igarashi, Chihiro Funamoto, Hiromitsu Nakauchi, Hunter B Fraser

Abstract read
In one paragraph

Article in Cell genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Alexander L StarrDepartment of Biology, Stanford University, Stanford, CA 94305, USA.
Toshiya NishimuraInstitute for Stem Cell Biology and Regenerative Medicine, Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA; Division of Stem Cell and Organoid Medicine, Department of Genome Biology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Kyomi J IgarashiDepartment of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA.
Chihiro FunamotoDivision of Stem Cell and Organoid Medicine, Department of Genome Biology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Hiromitsu NakauchiInstitute for Stem Cell Biology and Regenerative Medicine, Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA; Division of Stem Cell Therapy, Distinguished Professor Unit, The Institute of Medical Science, The University of Tokyo, Minato-ku, Tokyo 108-8639, Japan.
Hunter B FraserDepartment of Biology, Stanford University, Stanford, CA 94305, USA. Electronic address: hbfraser@stanford.edu.

Funding

Investigating human cis-regulatory evolution with hybrid iPS cellsR01HG012285 · NHGRI · STANFORD UNIVERSITY · PI FRASER, HUNTER B · 2022 to 2025
$2.8M
Understanding the developmental xenobarrierR01DK121851 · NIDDK · STANFORD UNIVERSITY · PI NAKAUCHI, HIROMITSU · 2020 to 2022
$1.2M
NHGRI NIH HHS R01 HG012285NIDDK NIH HHS R01 DK121851
6 · The paper itself

Abstract

A long-standing question in biology is the extent to which cells function autonomously as opposed to requiring interactions with other cells or environmental factors. Here, we develop a framework to use interspecies chimeras to precisely decompose evolutionary divergence in any cellular trait into cell-intrinsic and cell-extrinsic components. Applying this framework to thousands of gene expression levels in reciprocal rat-mouse chimeras, we found that most divergence is cell intrinsic, though extrinsic factors also play an integral role. For example, cell-extrinsic regulation of a transcription factor can propagate to its target genes, leading to cell-type-specific extrinsic regulation of both their mRNA and their protein levels. We also show that imprinted genes are dramatically misexpressed in chimeras, suggesting a mismatch between rapidly evolving intrinsic and extrinsic imprinting mechanisms. Overall, our conceptual framework opens up new avenues to investigate the mechanistic basis of the evolution, development, and regulation of myriad cellular traits in any multicellular organism.

Indexed as

Biological EvolutionEvolution, MolecularAnimalsChimeraGenomic ImprintingMiceRatsTranscription FactorsTranscription Factorsautonomouschimeradevelopmentevolutionextrinsicgene expressionimprintingintrinsicmouserat

Identifiers

PMID40446803
PMCPMC12366658

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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.