Evidence map›Paper›PMID 37873105›Full record

ArticlebioRxiv : the preprint server for biology2023

The genetic basis of novel trait gain in walking fish.

Amy L Herbert, Corey Ah Allard, Matthew J McCoy, Julia I Wucherpfennig, Stephanie P Krueger, Heidi I Chen, Allex N Gourlay, Kohle D Jackson, Lisa A Abbo, Scott H Bennett and 4 more

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

14 authors at 6 institutions in 1 country.

Amy L HerbertDepartment of Developmental Biology, Stanford University School of Medicine, Stanford CA 94305 USA.
Corey Ah AllardDepartment of Molecular and Cellular Biology, Harvard University, Cambridge MA 02138 USA.
Matthew J McCoyDepartment of Pathology, Stanford University School of Medicine, Stanford CA 94305 USA.
Julia I WucherpfennigDepartment of Developmental Biology, Stanford University School of Medicine, Stanford CA 94305 USA.
Stephanie P KruegerDepartment of Molecular and Cellular Biology, Harvard University, Cambridge MA 02138 USA.
Heidi I ChenDepartment of Developmental Biology, Stanford University School of Medicine, Stanford CA 94305 USA.
Allex N GourlayRoger Williams University, Bristol, RI 02809 USA.
Kohle D JacksonDepartment of Developmental Biology, Stanford University School of Medicine, Stanford CA 94305 USA.
Lisa A AbboMarine Biological Laboratory, Woods Hole, MA, 02543 USA.
Scott H BennettMarine Biological Laboratory, Woods Hole, MA, 02543 USA.
Joshua D SearsRoger Williams University, Bristol, RI 02809 USA.
Andrew L RhyneRoger Williams University, Bristol, RI 02809 USA.
Nicholas W BellonoDepartment of Molecular and Cellular Biology, Harvard University, Cambridge MA 02138 USA.
David M KingsleyHoward Hughes Medical Institute, Stanford University School of Medicine, Stanford CA 94305 USA.
Stanford University · USHarvard University · USRoger Williams University · USMarine Biological Laboratory · USHoward Hughes Medical Institute · USStanford Medicine · US

Funding

Molecular Mechanisms of Integrative Signal TransductionR35GM142697 · NIGMS · HARVARD UNIVERSITY · PI Nicholas Bellono · 2021 to 2026
$2.6M
NIGMS NIH HHS R35 GM142697
6 · The paper itself

Abstract

A major goal in biology is to understand how organisms evolve novel traits. Multiple studies have identified genes contributing to regressive evolution, the loss of structures that existed in a recent ancestor. However, fewer examples exist for genes underlying constructive evolution, the gain of novel structures and capabilities in lineages that previously lacked them. Sea robins are fish that have evolved enlarged pectoral fins, six mobile locomotory fin rays (legs) and six novel macroscopic lobes in the central nervous system (CNS) that innervate the corresponding legs. Here, we establish successful husbandry and use a combination of transcriptomics, CRISPR-Cas9 editing, and behavioral assays to identify key transcription factors that are required for leg formation and function in sea robins. We also generate hybrids between two sea robin species with distinct leg morphologies and use allele-specific expression analysis and gene editing to explore the genetic basis of species-specific trait diversity, including a novel sensory gain of function. Collectively, our study establishes sea robins as a new model for studying the genetic basis of novel organ formation, and demonstrates a crucial role for the conserved limb gene

Identifiers

PMID37873105
PMCPMC10592820
OpenAlexW4387655010

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.