Evidence map›Paper›PMID 35089417›Full record

ArticleHuman genetics2022

BMP3 is a novel locus involved in the causality of ocular coloboma.

Sabrina C Fox, Sonya A Widen, Mika Asai-Coakwell, Serhiy Havrylov, Matthew Benson, Lisa B Prichard, Pranidhi Baddam, Daniel Graf, Ordan J Lehmann, Andrew J Waskiewicz

Abstract read
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In one paragraph

Article in Human genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Zfp503/Nlz2 Is Required for RPE Differentiation and Optic Fissure Closure.Investigative ophthalmology & visual science · 2022
    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

10 authors at 3 institutions in 3 countries.

Sabrina C Fox *Department of Biological Sciences, University of Alberta, 11455 Saskatchewan Drive, Edmonton, AB, T6G 2E9, Canada.
Sonya A Widen *Department of Biological Sciences, University of Alberta, 11455 Saskatchewan Drive, Edmonton, AB, T6G 2E9, Canada.
Mika Asai-CoakwellDepartment of Animal and Poultry and Animal Science, University of Saskatchewan, Saskatoon, SK, Canada.
Serhiy HavrylovDepartment of Medical Genetics, University of Alberta, Edmonton, AB, Canada.
Matthew BensonDepartment of Medical Genetics, University of Alberta, Edmonton, AB, Canada.
Lisa B PrichardDepartment of Biological Sciences, MacEwan University, Edmonton, AB, Canada.
Pranidhi BaddamDepartment of Dentistry, University of Alberta, Edmonton, AB, Canada.
Daniel GrafDepartment of Medical Genetics, University of Alberta, Edmonton, AB, Canada.
Ordan J LehmannWomen and Children's Health Research Institute, University of Alberta, Edmonton, AB, Canada.
Andrew J WaskiewiczDepartment of Biological Sciences, University of Alberta, 11455 Saskatchewan Drive, Edmonton, AB, T6G 2E9, Canada. aw@ualberta.ca.ORCID http://orcid.org/0000-0002-5306-0643
University of Alberta · CAInstitute of Molecular Biotechnology · ATMacEwan University · CA

Funding

Natural Sciences and Engineering Research Council of Canada NSERC RGPIN-2016-04682Women and Children's Health Research Institute UOFAB WCHRIIG 2879
6 · The paper itself

Abstract

Coloboma, a congenital disorder characterized by gaps in ocular tissues, is caused when the choroid fissure fails to close during embryonic development. Several loci have been associated with coloboma, but these represent less than 40% of those that are involved with this disease. Here, we describe a novel coloboma-causing locus, BMP3. Whole exome sequencing and Sanger sequencing of patients with coloboma identified three variants in BMP3, two of which are predicted to be disease causing. Consistent with this, bmp3 mutant zebrafish have aberrant fissure closure. bmp3 is expressed in the ventral head mesenchyme and regulates phosphorylated Smad3 in a population of cells adjacent to the choroid fissure. Furthermore, mutations in bmp3 sensitize embryos to Smad3 inhibitor treatment resulting in open choroid fissures. Micro CT scans and Alcian blue staining of zebrafish demonstrate that mutations in bmp3 cause midface hypoplasia, suggesting that bmp3 regulates cranial neural crest cells. Consistent with this, we see active Smad3 in a population of periocular neural crest cells, and bmp3 mutant zebrafish have reduced neural crest cells in the choroid fissure. Taken together, these data suggest that Bmp3 controls Smad3 phosphorylation in neural crest cells to regulate early craniofacial and ocular development.

Indexed as

ColobomaAnimalsEyeNeural CrestZebrafishZebrafish ProteinsZebrafish Proteins

Identifiers

PMID35089417
OpenAlexW4220805276

What OpenQuestion 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 OpenQuestion graph.