Evidence map›Paper›PMID 37333085›Full record

ArticlebioRxiv : the preprint server for biology2023

Lineage motifs: developmental modules for control of cell type proportions.

Martin Tran, Amjad Askary, Michael B Elowitz

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. 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, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Martin TranDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Amjad AskaryDepartment of Molecular, Cell and Developmental Biology, University of California Los Angeles, Los Angeles, CA 90095, USA.
Michael B ElowitzDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
California Institute of Technology · USUniversity of California, Los Angeles · US

Funding

MEMOIR: Recording, and in situ readout of cell lineage and transcriptional historyR01MH116508 · NIMH · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI CAI, LONG, ELOWITZ, MICHAEL B · 2017 to 2021
$6.9M
Synthetic recording and in situ readout of cell lineage and molecular history in mammalian retinaR00EY031782 · NEI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ASKARY, AMJAD · 2022 to 2024
$747k
Determining the cell fate programs of mammalian retina developmentF31EY033220 · NEI · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI TRAN, MARTIN · 2021 to 2024
$189k
Synthetic recording and in situ readout of cell lineage and molecular history in mammalian retinaK99EY031782 · NEI · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI ASKARY, AMJAD · 2020 to 2020
$119k
NEI NIH HHS F31 EY033220NEI NIH HHS K99 EY031782NEI NIH HHS R00 EY031782NIMH NIH HHS R01 MH116508
6 · The paper itself

Abstract

In multicellular organisms, cell types must be produced and maintained in appropriate proportions. One way this is achieved is through committed progenitor cells that produce specific sets of descendant cell types. However, cell fate commitment is probabilistic in most contexts, making it difficult to infer progenitor states and understand how they establish overall cell type proportions. Here, we introduce Lineage Motif Analysis (LMA), a method that recursively identifies statistically overrepresented patterns of cell fates on lineage trees as potential signatures of committed progenitor states. Applying LMA to published datasets reveals spatial and temporal organization of cell fate commitment in zebrafish and rat retina and early mouse embryo development. Comparative analysis of vertebrate species suggests that lineage motifs facilitate adaptive evolutionary variation of retinal cell type proportions. LMA thus provides insight into complex developmental processes by decomposing them into simpler underlying modules.

Indexed as

blastocyst developmentcell fate correlationscell type proportionsDevelopmental programslineage tree analysismotif analysisPareto optimalityretina development

Identifiers

PMID37333085
PMCPMC10274800
OpenAlexW4379744005

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.