Evidence map›Paper›PMID 42748521›Full record

ArticleDifferentiation; research in biological diversity2026

The lipid raft-linker gene Raftlin-2 is expressed in migrating neural crest cells.

Mallorie P Jenne, Ilya Grabylnikov, Michael L Piacentino

Abstract read
In one paragraph

Article in Differentiation; research in biological diversity, 2026. 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

3 authors.

Mallorie P JenneDepartment of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA; Program in Biochemistry, Cellular, and Molecular Biology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.
Ilya GrabylnikovDepartment of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.
Michael L PiacentinoDepartment of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA; Program in Biochemistry, Cellular, and Molecular Biology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA; Center for Functional Anatomy and Evolution, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA. Electronic address: michaelpiacentino@jhmi.edu.

Funding

Determining how membrane fluidity regulates embryonic cell migrationR35GM155257 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI Michael Louis Piacentino · 2024 to 2026
$1.2M
Characterizing the cranial neural crest response to BMP signaling through gastrulation and neurulationR00DE029240 · NIDCR · JOHNS HOPKINS UNIVERSITY · PI PIACENTINO, MICHAEL LOUIS · 2023 to 2025
$873k
Determining the role of Raftlin-2 in neural crest cell specification and migrationF31DE035770 · NIDCR · JOHNS HOPKINS UNIVERSITY · PI Mallorie Patricia Jenne · 2025 to 2026
$101k
NIDCR NIH HHS F31 DE035770NIDCR NIH HHS R00 DE029240NIGMS NIH HHS R35 GM155257
6 · The paper itself

Abstract

Transient plasma membrane domains called lipid rafts have emerged as important regulators of signal transduction. These territories are formed by lipid-lipid and lipid-protein interactions, and these local interactions can be scaffolded by resident lipid raft organizing protein family members. While roles for lipid rafts have been described for multiple signaling pathways in many contexts, their in vivo prevalence and roles during embryonic development remain incompletely understood. Here we examined gene expression for the Raftlin family of lipid raft organizing proteins, Raftlin-1 (RFTN1) and Raftlin-2 (RFTN2), over the course of early vertebrate development, with a focus on neural crest cell dynamics. By analyzing transcriptomic data across vertebrate species, we identified conserved patterns of RFTN1 and RFTN2 expression across species, where RFTN1 is broadly expressed at low levels, while RFTN2 is distinctly enriched in neural crest cells. We used fluorescent in situ hybridization to spatially define Raftlin gene family expression patterns in the early avian embryo. Our results show that RFTN1 is broadly expressed with periods of enrichment in the developing paraxial mesoderm. In contrast, RFTN2 expression is strongly enriched in neural crest cells, beginning during specification and persisting through migration, with additional expression in both the cranial and intermediate mesoderm. Together, these patterns suggest that Raftlin proteins may play important roles in regulating signaling during development with potential roles in somitogenesis and in neural crest and mesodermal cell migrations.

Indexed as

Cell migrationLipid raftsNeural crestRaftlin-1Raftlin-2

Identifiers

PMID42748521
PMCPMC13615771

What Socratic holds

Textmetadata
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 Socratic graph.