Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2006-1-9
pubmed:abstractText
Msx and Dlx homeoproteins control the morphogenesis and organization of craniofacial skeletal structures, specifically those derived from the pharyngeal arches. In vitro Msx and Dlx proteins have opposing transcriptional properties and form heterodimeric complexes via their homeodomain with reciprocal functional repression. In this report we examine the skeletal phenotype of Msx1; Dlx5 double knock-out (DKO) mice in relationship with their expression territories during craniofacial development. Co-expression of Dlx5 and Msx1 is only observed in embryonic tissues in which these genes have independent functions, and thus direct protein interactions are unlikely to control morphogenesis of the cranium. The DKO craniofacial phenotypes indicate a complex interplay between these genes, acting independently (mandible and middle ear), synergistically (deposition of bone tissue) or converging on the same morphogenetic process (palate growth and closure). In the latter case, the absence of Dlx5 rescues in part the Msx1-dependent defects in palate growth and elevation. At the basis of this effect, our data implicate the Bmp (Bmp7, Bmp4)/Bmp antagonist (Follistatin) signal: in the Dlx5(-/-) palate changes in the expression level of Bmp7 and Follistatin counteract the reduced Bmp4 expression. These results highlight the importance of precise spatial and temporal regulation of the Bmp/Bmp antagonist system during palate closure.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0925-4773
pubmed:author
pubmed:issnType
Print
pubmed:volume
123
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3-16
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:16330189-Animals, pubmed-meshheading:16330189-Base Sequence, pubmed-meshheading:16330189-Bone Morphogenetic Protein 7, pubmed-meshheading:16330189-Bone Morphogenetic Proteins, pubmed-meshheading:16330189-Craniofacial Abnormalities, pubmed-meshheading:16330189-DNA, Complementary, pubmed-meshheading:16330189-Ear, Middle, pubmed-meshheading:16330189-Facial Bones, pubmed-meshheading:16330189-Gene Expression Regulation, Developmental, pubmed-meshheading:16330189-Homeodomain Proteins, pubmed-meshheading:16330189-MSX1 Transcription Factor, pubmed-meshheading:16330189-Mandible, pubmed-meshheading:16330189-Mice, pubmed-meshheading:16330189-Mice, Knockout, pubmed-meshheading:16330189-Mice, Transgenic, pubmed-meshheading:16330189-Palate, pubmed-meshheading:16330189-Phenotype, pubmed-meshheading:16330189-Signal Transduction, pubmed-meshheading:16330189-Skull, pubmed-meshheading:16330189-Transforming Growth Factor beta
pubmed:year
2006
pubmed:articleTitle
Msx1 and Dlx5 act independently in development of craniofacial skeleton, but converge on the regulation of Bmp signaling in palate formation.
pubmed:affiliation
Evolution des Régulations Endocriniennes, CNRS UMR5166, Museum National d'Histoire Naturelle, Paris, France.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't