Evidence map›Paper›PMID 32320685›Full record

ArticleDevelopmental biology2020

Apcdd1 is a dual BMP/Wnt inhibitor in the developing nervous system and skin.

Alin Vonica, Neha Bhat, Keith Phan, Jinbai Guo, Lăcrimioara Iancu, Jessica A Weber, Amir Karger, John W Cain, Etienne C E Wang, Gina M DeStefano and 5 more

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

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  15. Structure of WNT inhibitor adenomatosis polyposis coli down-regulated 1 (APCDD1), a cell-surface lipid-binding protein.Proceedings of the National Academy of Sciences of the United States of America · 2023
    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

15 authors at 8 institutions in 3 countries.

Alin VonicaDepartments of Genetics and Development, and Dermatology, Columbia University Medical Center, New York, NY, 10032, USA; Department of Biology, The Nazareth College, Rochester, NY, 14618, USA.
Neha BhatDepartment of Biology, Texas A&M University, College Station, TX, 7783-3258, USA; Yale Cardiovascular Research Center, Yale School of Medicine, New Haven, CT, 06511, USA.
Keith PhanDepartment of Neurobiology, University of California, Los Angeles, CA, 90095-7239, USA.
Jinbai GuoDepartment of Biology, Texas A&M University, College Station, TX, 7783-3258, USA.
Lăcrimioara IancuInstitut für Algebra und Zahlentheorie, Universität Stuttgart, D-70569, Stuttgart, Germany; Institute of Mathematics, University of Aberdeen, Aberdeen, AB24 3UE, Scotland, UK.
Jessica A WeberDepartment of Genetics, Harvard Medical School, Boston, MA, 02115, USA.
Amir KargerIT-Research Computing, Harvard Medical School, Boston, MA, 02115, USA.
John W CainDepartment of Mathematics, Harvard University, Cambridge, MA, 02138, USA.
Etienne C E WangDepartments of Genetics and Development, and Dermatology, Columbia University Medical Center, New York, NY, 10032, USA.
Gina M DeStefanoDepartments of Genetics and Development, and Dermatology, Columbia University Medical Center, New York, NY, 10032, USA.
Anne H O'Donnell-LuriaProgram in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, 02115, USA.
Angela M ChristianoDepartments of Genetics and Development, and Dermatology, Columbia University Medical Center, New York, NY, 10032, USA. Electronic address: amc65@cumc.columbia.edu.
Bruce RileyDepartment of Biology, Texas A&M University, College Station, TX, 7783-3258, USA. Electronic address: briley@bio.tamu.edu.
Samantha J ButlerDepartment of Neurobiology, University of California, Los Angeles, CA, 90095-7239, USA. Electronic address: butlersj@ucla.edu.
Victor LuriaDepartments of Genetics and Development, and Dermatology, Columbia University Medical Center, New York, NY, 10032, USA; Department of Systems Biology, Harvard Medical School, Boston, MA, 02115, USA. Electronic address: Victor_Luria@hms.harvard.edu.
Harvard University · USColumbia University Irving Medical Center · USTexas A&M University · USUniversity of California, Los Angeles · USBroad Institute · USNazareth College · USUniversity of Stuttgart · DEYale University · US

Funding

The Child Heath Research CenterK12HD052896 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI Wendy K Chung · 2007 to 2026
$7.9M
GENETIC ANALYSIS OF INNER EAR DEVELOPMENT IN ZEBRAFISHR01DC003806 · NIDCD · TEXAS A&M UNIVERSITY SYSTEM · PI RILEY, BRUCE B · 1998 to 2023
$7.2M
Understanding the Biology of Chronic Ulcers: Histological and Molecular Basis...P30AR044535 · NIAMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI BICKERS, DAVID RINSEY · 1997 to 2015
$6.9M
Systems Analysis of cell type differentiation in Xenopus developmentR01HD073104 · NICHD · HARVARD MEDICAL SCHOOL · PI KIRSCHNER, MARC WALLACE, PESHKIN, LEON · 2012 to 2022
$6.7M
Proteomics of Cell Signaling in Embryogenesis.R01HD091846 · NICHD · HARVARD MEDICAL SCHOOL · PI GYGI, STEVEN P, KIRSCHNER, MARC WALLACE · 2017 to 2021
$3.1M
Diverse roles of the Bone Morphogenetic Proteins in the developing spinal cordR01NS085097 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BUTLER, SAMANTHA J · 2014 to 2018
$1.7M
Genetic Analysis of Alopecia AreataR01AR052579 · NIAMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CHRISTIANO, ANGELA M · 2006 to 2009
$1.3M
Targets of a cytidine deaminase required for left-right axis in XenopusR03HD057334 · NICHD · ROCKEFELLER UNIVERSITY · PI VONICA, ALIN · 2009 to 2010
$168k
NIAMS NIH HHS P30 AR044535NIAMS NIH HHS R01 AR052579NICHD NIH HHS K12 HD052896NICHD NIH HHS R01 HD073104NICHD NIH HHS R01 HD091846NICHD NIH HHS R03 HD057334NIDCD NIH HHS R01 DC003806NINDS NIH HHS R01 NS085097
6 · The paper itself

Abstract

Animal development and homeostasis depend on precise temporal and spatial intercellular signaling. Components shared between signaling pathways, generally thought to decrease specificity, paradoxically can also provide a solution to pathway coordination. Here we show that the Bone Morphogenetic Protein (BMP) and Wnt signaling pathways share Apcdd1 as a common inhibitor and that Apcdd1 is a taxon-restricted gene with novel domains and signaling functions. Previously, we showed that Apcdd1 inhibits Wnt signaling (Shimomura et al., 2010), here we find that Apcdd1 potently inhibits BMP signaling in body axis formation and neural differentiation in chicken, frog, zebrafish. Furthermore, we find that Apcdd1 has an evolutionarily novel protein domain. Our results from experiments and modeling suggest that Apcdd1 may coordinate the outputs of two signaling pathways that are central to animal development and human disease.

Indexed as

Body PatterningWnt Signaling PathwayAnimalsBone Morphogenetic ProteinsEmbryo, NonmammalianMembrane GlycoproteinsProtein DomainsXenopus laevisXenopus ProteinsApcdd1 protein, XenopusBone Morphogenetic ProteinsMembrane GlycoproteinsXenopus ProteinsApcdd1Bi-functional proteinChickenEmbryonic developmentMouseWnt and BMP signaling InhibitorXenopusZebrafish

Identifiers

PMID32320685
PMCPMC7307705
OpenAlexW3017286629

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.