Evidence map›Paper›PMID 38193440›Full record

ArticleeLife2024

Intrinsic and extrinsic cues time somite progenitor contribution to the vertebrate primary body axis.

Lara Busby, Guillermo Serrano Nájera, Benjamin John Steventon

Open access · goldAbstract read
In one paragraph

Article in eLife, 2024. 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
1.2field-weighted citation impact, top 24% of its field
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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
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

3 authors at 1 institution in 2 countries.

Lara BusbyDepartment of Genetics, University of Cambridge, Cambridge, United Kingdom.ORCID https://orcid.org/0000-0003-0705-1364
Guillermo Serrano NájeraDepartment of Genetics, University of Cambridge, Cambridge, United Kingdom.ORCID https://orcid.org/0000-0001-5841-8408
Benjamin John SteventonDepartment of Genetics, University of Cambridge, Cambridge, United Kingdom.ORCID https://orcid.org/0000-0001-7838-839X
University of Cambridge · GB

Funding

Biotechnology and Biological Sciences Research Council StudentshipWellcome TrustWellcome Trust 10.35802/109408Wellcome Trust 109408/Z/15/ZWellcome Trust 225360/Z/22/Z
6 · The paper itself

Abstract

During embryonic development, the timing of events at the cellular level must be coordinated across multiple length scales to ensure the formation of a well-proportioned body plan. This is clear during somitogenesis, where progenitors must be allocated to the axis over time whilst maintaining a progenitor population for continued elaboration of the body plan. However, the relative importance of intrinsic and extrinsic signals in timing progenitor addition at the single-cell level is not yet understood. Heterochronic grafts from older to younger embryos have suggested a level of intrinsic timing whereby later staged cells contribute to more posterior portions of the axis. To determine the precise step at which cells are delayed, we performed single-cell transcriptomic analysis on heterochronic grafts of somite progenitors in the chicken embryo. This revealed a previously undescribed cell state within which heterochronic grafted cells are stalled. The delayed exit of older cells from this state correlates with expression of posterior

Indexed as

CuesSomitesAnimalsChick EmbryoGene Expression Regulation, DevelopmentalGenes, HomeoboxVertebrateschickendevelopmental biologygastrulationHoxprimitive streaksomitogenesistiming

Identifiers

PMID38193440
PMCPMC10834026
OpenAlexW4390727926

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.