Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1999-5-6
pubmed:databankReference
pubmed:abstractText
The bone morphogenetic proteins (BMPs) play critical roles in patterning the early embryo and in the development of many organs and tissues. We have identified a new member of this multifunctional gene family, BMP-11, which is most closely related to GDF-8/myostatin. During mouse embryogenesis, BMP-11 is first detected at 9.5 dpc in the tail bud with expression becoming stronger as development proceeds. At 10.0 dpc, BMP-11 is expressed in the distal and posterior region of the limb bud and later localizes to the mesenchyme between the skeletal elements. BMP-11 is also expressed in the developing nervous system, in the dorsal root ganglia, and dorsal lateral region of the spinal cord. To assess the biological activity of BMP-11, we tested the protein in the Xenopus ectodermal explant (animal cap) assay. BMP-11 induced axial mesodermal tissue (muscle and notochord) in a dose-dependent fashion. At higher concentrations, BMP-11 also induced neural tissue. Interestingly, the activin antagonist, follistatin, but not noggin, an antagonist of BMPs 2 and 4, inhibited BMP-11 activity on animal caps. Our data suggest that in Xenopus embryos, BMP-11 acts more like activin, inducing dorsal mesoderm and neural tissue, and less like other family members such as BMPs 2, 4, and 7, which are ventralizing and anti-neuralizing signals. Taken together, these data suggest that during vertebrate embryogenesis, BMP-11 plays a unique role in patterning both mesodermal and neural tissues.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0012-1606
pubmed:author
pubmed:copyrightInfo
Copyright 1999 Academic Press.
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
208
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
222-32
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:10075854-Amino Acid Sequence, pubmed-meshheading:10075854-Animals, pubmed-meshheading:10075854-Bone Morphogenetic Proteins, pubmed-meshheading:10075854-Carrier Proteins, pubmed-meshheading:10075854-Cloning, Molecular, pubmed-meshheading:10075854-Extremities, pubmed-meshheading:10075854-Follistatin, pubmed-meshheading:10075854-Gene Expression Regulation, Developmental, pubmed-meshheading:10075854-Glycoproteins, pubmed-meshheading:10075854-Histocytochemistry, pubmed-meshheading:10075854-Humans, pubmed-meshheading:10075854-In Situ Hybridization, pubmed-meshheading:10075854-Mesoderm, pubmed-meshheading:10075854-Mice, pubmed-meshheading:10075854-Molecular Sequence Data, pubmed-meshheading:10075854-Proteins, pubmed-meshheading:10075854-RNA, Messenger, pubmed-meshheading:10075854-Sequence Analysis, DNA, pubmed-meshheading:10075854-Sequence Homology, Amino Acid, pubmed-meshheading:10075854-Spinal Cord, pubmed-meshheading:10075854-Tail, pubmed-meshheading:10075854-Tissue Transplantation, pubmed-meshheading:10075854-Xenopus, pubmed-meshheading:10075854-Xenopus Proteins
pubmed:year
1999
pubmed:articleTitle
A novel BMP expressed in developing mouse limb, spinal cord, and tail bud is a potent mesoderm inducer in Xenopus embryos.
pubmed:affiliation
Genetics Institute, Inc., 87 Cambridge Park Drive, Cambridge, Massachusetts 02140, USA. lgamer@genetics.com
pubmed:publicationType
Journal Article, Comparative Study