Evidence map›Paper›PMID 19096511›Full record

ArticlePLoS genetics2008

Shaping skeletal growth by modular regulatory elements in the Bmp5 gene.

Catherine Guenther, Luiz Pantalena-Filho, David M Kingsley

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

36 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Isolation and characterization of bone mesenchymal cell small extracellular vesicles using a novel mouse model.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Application of BMP in Bone Tissue Engineering.Frontiers in bioengineering and biotechnology · 2022
    Review
  10. Article
  11. Making and shaping endochondral and intramembranous bones.Developmental dynamics : an official publication of the American Association of Anatomists · 2021
    Review
  12. Growth Factor Roles in Soft Tissue Physiology and Pathophysiology.Advances in experimental medicine and biology · 2021
    Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
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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

3 authors at 1 institution in 1 country.

Catherine GuentherDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA, USA.
Luiz Pantalena-Filho
David M Kingsley
Stanford University · US

Funding

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
Howard Hughes Medical InstituteNIAMS NIH HHS R01 AR042236NIAMS NIH HHS R01 AR42236NIAMS NIH HHS R37 AR042236
6 · The paper itself

Abstract

Cartilage and bone are formed into a remarkable range of shapes and sizes that underlie many anatomical adaptations to different lifestyles in vertebrates. Although the morphological blueprints for individual cartilage and bony structures must somehow be encoded in the genome, we currently know little about the detailed genomic mechanisms that direct precise growth patterns for particular bones. We have carried out large-scale enhancer surveys to identify the regulatory architecture controlling developmental expression of the mouse Bmp5 gene, which encodes a secreted signaling molecule required for normal morphology of specific skeletal features. Although Bmp5 is expressed in many skeletal precursors, different enhancers control expression in individual bones. Remarkably, we show here that different enhancers also exist for highly restricted spatial subdomains along the surface of individual skeletal structures, including ribs and nasal cartilages. Transgenic, null, and regulatory mutations confirm that these anatomy-specific sequences are sufficient to trigger local changes in skeletal morphology and are required for establishing normal growth rates on separate bone surfaces. Our findings suggest that individual bones are composite structures whose detailed growth patterns are built from many smaller lineage and gene expression domains. Individual enhancers in BMP genes provide a genomic mechanism for controlling precise growth domains in particular cartilages and bones, making it possible to separately regulate skeletal anatomy at highly specific locations in the body.

Indexed as

Bone DevelopmentRegulatory Sequences, Nucleic AcidAnimalsBone Morphogenetic Protein 5Enhancer Elements, GeneticGene ExpressionMiceMice, Inbred C57BLMice, TransgenicNasal CartilagesProtein Structure, TertiaryRibsSignal TransductionBmp5 protein, mouseBone Morphogenetic Protein 5

Identifiers

PMID19096511
PMCPMC2592695
OpenAlexW2001929897

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.