Evidence map›Paper›PMID 40140914›Full record

ArticleBMC biology2025

A combination of transcriptomics and epigenomics identifies genes and regulatory elements involved in embryonic tail development in the mouse.

Yong-Xuan Chen, Xiu-Ping Zhang, David N Cooper, Dong-Dong Wu, Wan-Dong Bao

Abstract read
In one paragraph

Article in BMC biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. The lipid raft-linker gene Raftlin-2 is expressed in migrating neural crest cells.Differentiation; research in biological diversity · 2026
    Article
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

5 authors.

Yong-Xuan Chen *State Key Laboratory of Genetic Resources and Evolution, Kunming Natural History Museum of Zoology, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, 650201, China.
Xiu-Ping Zhang *State Key Laboratory of Genetic Resources and Evolution, Kunming Natural History Museum of Zoology, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, 650201, China.
David N CooperInstitute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, Wales, UK.
Dong-Dong WuState Key Laboratory of Genetic Resources and Evolution, Kunming Natural History Museum of Zoology, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, 650201, China. wudongdong@mail.kiz.ac.cn.
Wan-Dong BaoState Key Laboratory of Genetic Resources and Evolution, Kunming Natural History Museum of Zoology, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, 650201, China. baowandong@mail.kiz.ac.cn.

Funding

Applied Basic Research Foundation of Yunnan Province 2019FA008Applied Basic Research Foundation of Yunnan Province 2019FI010Applied Basic Research Foundation of Yunnan Province 2019FJ003Applied Basic Research Foundation of Yunnan Province 202305AH340006Applied Basic Research Foundation of Yunnan Province 202401AT070303West Light Foundation, Chinese Academy of Sciences xbzg-zdsys-202213
6 · The paper itself

Abstract

backgroundThe post-anal tail is a common physical feature of vertebrates including mammals. Although it exhibits rich phenotypic diversity, its development has been evolutionarily conserved as early as the embryonic period. Genes participating in embryonic tail morphogenesis have hitherto been widely explored on the basis of experimental discovery, whereas the associated cis-regulatory elements (CREs) have not yet been systematically investigated for vertebrate/mammalian tail development.

resultsHere, utilizing high-throughput sequencing schemes pioneered in mice, we profiled the dynamic transcriptome and CREs marked by active histone modifications during embryonic tail morphogenesis. Temporal and spatial disparity analyses revealed the genes specific to tail development and their putative CREs, which facilitated the identification of novel molecular expression features and potential regulatory influence of non-coding loci including long non-coding RNA (lncRNA) genes and CREs. Moreover, these identified sets of multi-omics data supply genetic clues for understanding the regulatory effects of relevant signaling pathways (such as Fgf, Wnt) dominating embryonic tail morphogenesis.

conclusionsOur work brings new insights and provides exploitable fundamental datasets for the elucidation of the complex genetic mechanisms responsible for the formation of the vertebrate/mammalian tail.

Indexed as

Embryonic DevelopmentRegulatory Sequences, Nucleic AcidTailTranscriptomeAnimalsEpigenomicsGene Expression ProfilingGene Expression Regulation, DevelopmentalMiceRNA, Long NoncodingRNA, Long NoncodingCis-regulatory elementEmbryonic tail morphogenesisEpigenomic histone modificationTranscriptomeVertebrate/mammal/mouse

Identifiers

PMID40140914
PMCPMC11948857

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.