Evidence map›Paper›PMID 34826632›Full record

ArticleBone2022

Characterization of mouse Bmp5 regulatory injury element in zebrafish wound models.

Ian S Heller, Catherine A Guenther, Ana M Meireles, William S Talbot, David M Kingsley

Open access · greenAbstract read
In one paragraph

Article in Bone, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 36% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

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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 at 1 institution in 1 country.

Ian S HellerDepartment of Developmental Biology, Stanford University School of Medicine, United States of America.
Catherine A GuentherDepartment of Developmental Biology, Stanford University School of Medicine, United States of America; Howard Hughes Medical Institute, Stanford University School of Medicine, United States of America.
Ana M MeirelesDepartment of Developmental Biology, Stanford University School of Medicine, United States of America.
William S TalbotDepartment of Developmental Biology, Stanford University School of Medicine, United States of America.
David M KingsleyDepartment of Developmental Biology, Stanford University School of Medicine, United States of America; Howard Hughes Medical Institute, Stanford University School of Medicine, United States of America. Electronic address: kingsley@stanford.edu.
Stanford University · US

Funding

Genetic and cellular analysis of glial development and function in vertebratesR35NS111584 · NINDS · STANFORD UNIVERSITY · PI WILLIAM S TALBOT · 2019 to 2026
$4.3M
Genetic Analysis of Bone Morphogenic ProteinsR37AR042236 · NIAMS · STANFORD UNIVERSITY · PI KINGSLEY, DAVID M · 2002 to 2011
$3.4M
GENETIC ANALYSIS OF BONE MORPHOGENETIC PROTEINSR01AR042236 · NIAMS · STANFORD UNIVERSITY · PI KINGSLEY, DAVID M · 1993 to 2001
$915k
NIAMS NIH HHS R01 AR042236NIAMS NIH HHS R37 AR042236NINDS NIH HHS R35 NS111584
6 · The paper itself

Abstract

Many key signaling molecules used to build tissues during embryonic development are re-activated at injury sites to stimulate tissue regeneration and repair. Bone morphogenetic proteins provide a classic example, but the mechanisms that lead to reactivation of BMPs following injury are still unknown. Previous studies have mapped a large "injury response element" (IRE) in the mouse Bmp5 gene that drives gene expression following bone fractures and other types of injury. Here we show that the large mouse IRE region is also activated in both zebrafish tail resection and mechanosensory hair cell injury models. Using the ability to test multiple constructs and image temporal and spatial dynamics following injury responses, we have narrowed the original size of the mouse IRE region by over 100 fold and identified a small 142 bp minimal enhancer that is rapidly induced in both mesenchymal and epithelial tissues after injury. These studies identify a small sequence that responds to evolutionarily conserved local signals in wounded tissues and suggest candidate pathways that contribute to BMP reactivation after injury.

Indexed as

Bone Morphogenetic ProteinsZebrafishAnimalsEmbryonic DevelopmentMiceRegulatory Sequences, Nucleic AcidSignal TransductionBone Morphogenetic ProteinsBMPFin regenerationGene regulationHair cell injuryInjury enhancerRegeneration

Identifiers

PMID34826632
PMCPMC9007314
OpenAlexW3216834406

What OpenQuestion holds

Textmetadata
LicenceTDM
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.