Evidence map›Paper›PMID 39198579›Full record

ArticleScientific reports2024

Splicing is dynamically regulated during limb development.

Sean Driscoll, Fjodor Merkuri, Frédéric J J Chain, Jennifer L Fish

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Ancestral intronic splicing regulatory elements in the SCNbioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. 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

4 authors.

Sean DriscollDepartment of Biological Sciences, University of Massachusetts Lowell, Lowell, MA, USA.
Fjodor MerkuriDepartment of Biological Sciences, University of Massachusetts Lowell, Lowell, MA, USA.
Frédéric J J ChainDepartment of Biological Sciences, University of Massachusetts Lowell, Lowell, MA, USA. Frederic_Chain@uml.edu.
Jennifer L FishDepartment of Biological Sciences, University of Massachusetts Lowell, Lowell, MA, USA. Jennifer_Fish@uml.edu.

Funding

Molecular mechanisms underlying variation in severity of craniofacial diseaseR15DE026611 · NIDCR · UNIVERSITY OF MASSACHUSETTS LOWELL · PI FISH, JENNIFER LESLIE · 2017 to 2020
$823k
NIDCR NIH HHS R15 DE026611NIH HHS R15 DE026611-02
6 · The paper itself

Abstract

Modifications to highly conserved developmental gene regulatory networks are thought to underlie morphological diversification in evolution and contribute to human congenital malformations. Relationships between gene expression and morphology have been extensively investigated in the limb, where most of the evidence for alterations to gene regulation in development consists of pre-transcriptional mechanisms that affect expression levels, such as epigenetic alterations to regulatory sequences and changes to cis-regulatory elements. Here we report evidence that alternative splicing (AS), a post-transcriptional process that modifies and diversifies mRNA transcripts, is dynamic during limb development in two mammalian species. We evaluated AS patterns in mouse (Mus musculus) and opossum (Monodelphis domestica) across the three key limb developmental stages: the ridge, bud, and paddle. Our data show that splicing patterns are dynamic over developmental time and suggest differences between the two mammalian taxa. Additionally, multiple key limb development genes, including Fgf8, are differentially spliced across the three stages in both species, with expression levels of the conserved splice variants, Fgf8a and Fgf8b, changing across developmental time. Our data demonstrates that AS is a critical mediator of mRNA diversity in limb development and provides an additional mechanism for evolutionary tweaking of gene dosage.

Indexed as

Alternative SplicingExtremitiesFibroblast Growth Factor 8Gene Expression Regulation, DevelopmentalAnimalsMiceMonodelphisRNA, MessengerFgf8 protein, mouseFibroblast Growth Factor 8RNA, Messenger

Identifiers

PMID39198579
PMCPMC11358489

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Registered trials

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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.