Evidence map›Paper›PMID 20627960›Full record

ArticleDevelopment (Cambridge, England)2010

Scapula development is governed by genetic interactions of Pbx1 with its family members and with Emx2 via their cooperative control of Alx1.

Terence D Capellini, Giulia Vaccari, Elisabetta Ferretti, Sebastian Fantini, Mu He, Massimo Pellegrini, Laura Quintana, Giuseppina Di Giacomo, James Sharpe, Licia Selleri and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2010. 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
8.3field-weighted citation impact, top 2% 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, 72 citations in OpenAlex.

  1. Article
  2. Article
  3. Novel Insights into Emx2 and Dmrta2 Cooperation during Cortex Development and Evidence for Dmrta2 Function in the Choroid Plexus.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. A Method for Identifying Vesicle Transport Proteins Based on LibSVM and MRMD.Computational and mathematical methods in medicine · 2020
    Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. A century of development.American journal of physical anthropology · 2018
    Review
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

11 authors at 1 institution in 1 country.

Terence D CapelliniDepartment of Cell and Developmental Biology, Weill Medical College of Cornell University, 1300 York Avenue, New York, NY 10021, USA.
Giulia Vaccari
Elisabetta Ferretti
Sebastian Fantini
Mu He
Massimo Pellegrini
Laura Quintana
Giuseppina Di Giacomo
James Sharpe
Licia Selleri
Vincenzo Zappavigna
Cornell University · US

Funding

Mechanisms of Pbx-directed Genetic &Transcriptional Control of Limb DevelopmentR01HD043997 · NICHD · WEILL MEDICAL COLL OF CORNELL UNIV · PI SELLERI, LICIA · 2004 to 2016
$3.7M
Genetic and Transcriptional Control of Spleen DevelopmentR01HD061403 · NICHD · WEILL MEDICAL COLL OF CORNELL UNIV · PI SELLERI, LICIA · 2010 to 2014
$1.7M
CLONING OF THE Hol MUTATIONR21DE018031 · NIDCR · WEILL MEDICAL COLL OF CORNELL UNIV · PI SELLERI, LICIA · 2008 to 2009
$573k
Medical Research Council MC_U127574434NICHD NIH HHS 1R01HD061403-01NICHD NIH HHS 2R01HD043997-06NICHD NIH HHS R01 HD043997NICHD NIH HHS R01 HD061403NIDCR NIH HHS 3R21DE018031-02S1NIDCR NIH HHS R21 DE018031Telethon GGP05181
6 · The paper itself

Abstract

The genetic pathways underlying shoulder blade development are largely unknown, as gene networks controlling limb morphogenesis have limited influence on scapula formation. Analysis of mouse mutants for Pbx and Emx2 genes has suggested their potential roles in girdle development. In this study, by generating compound mutant mice, we examined the genetic control of scapula development by Pbx genes and their functional relationship with Emx2. Analyses of Pbx and Pbx1;Emx2 compound mutants revealed that Pbx genes share overlapping functions in shoulder development and that Pbx1 genetically interacts with Emx2 in this process. Here, we provide a biochemical basis for Pbx1;Emx2 genetic interaction by showing that Pbx1 and Emx2 can bind specific DNA sequences as heterodimers. Moreover, the expression of genes crucial for scapula development is altered in these mutants, indicating that Pbx genes act upstream of essential pathways for scapula formation. In particular, expression of Alx1, an effector of scapula blade patterning, is absent in all compound mutants. We demonstrate that Pbx1 and Emx2 bind in vivo to a conserved sequence upstream of Alx1 and cooperatively activate its transcription via this potential regulatory element. Our results establish an essential role for Pbx1 in genetic interactions with its family members and with Emx2 and delineate novel regulatory networks in shoulder girdle development.

Indexed as

Gene Expression Regulation, DevelopmentalMutationAnimalsBase SequenceBinding SitesCrosses, GeneticDimerizationDNA-Binding ProteinsEmpty Spiracles Homeobox ProteinsGene Expression ProfilingHomeodomain ProteinsMiceModels, GeneticMolecular Sequence DataPre-B-Cell Leukemia Transcription Factor 1ScapulaAlx1 protein, mouseDNA-Binding ProteinsEmpty Spiracles Homeobox ProteinsHomeodomain ProteinsPbx1 protein, mousePre-B-Cell Leukemia Transcription Factor 1Transcription Factors

Identifiers

PMID20627960
PMCPMC2927673
OpenAlexW2153499136

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.