Evidence map›Paper›PMID 40799603›Full record

ArticlebioRxiv : the preprint server for biology2025

Noise-driven morphogenesis independent of transcriptional regulatory programs.

Jack Toppen, Saeed Tavazoie

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

2 authors.

Jack ToppenDepartment of Biological Sciences, Columbia University, New York, NY 10027, USA.
Saeed TavazoieDepartment of Biological Sciences, Columbia University, New York, NY 10027, USA.ORCID 0000-0003-2183-4162

Funding

Stochastic tuning: a novel regulatory mechanism for cellular adaptationR01GM139215 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI TAVAZOIE, SAEED F · 2020 to 2023
$1.6M
NIGMS NIH HHS R01 GM139215
6 · The paper itself

Abstract

Development is widely understood as a deterministic process driven by transcriptional programs that specify cell fate and orchestrate morphogenesis. However, this view overlooks pervasive stochasticity in gene expression, often considered an obstacle to reliable tissue patterning. Here, we introduce stochastic tuning-driven morphogenesis (STM), an alternative conceptualization of development in which noisy gene expression is not a nuisance but the primary driving force-guiding cell fates toward optimal multicellular configurations by a trial-and-error process analogous to reinforcement learning. STM operates independently of fixed transcriptional programs, instead relying on convergence of sensory information into signaling hubs, which by reinforcing random transcriptional changes, prospectively and contextually fine-tune gene expression along key developmental milestones. STM offers a fundamentally different view of development-one in which stochastic gene expression enables real-time optimization of gene expression toward multicellular objectives, implementing a self-organizing process that is inherently resistant to molecular and environmental fluctuations.

Identifiers

PMID40799603
PMCPMC12340819

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.