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DAN is a secreted glycoprotein related to Xenopus cerberus

Identifieur interne : 00C922 ( Main/Exploration ); précédent : 00C921; suivant : 00C923

DAN is a secreted glycoprotein related to Xenopus cerberus

Auteurs : E. Stanley [Australie] ; C. Biben [Australie] ; S. Kotecha [Royaume-Uni] ; L. Fabri [Australie] ; S. Tajbakhsh [France] ; C-C. Wang [Australie] ; T. Hatzistavrou [Australie] ; B. Roberts [Australie] ; C. Drinkwater [Australie] ; M. Lah [Australie] ; M. Buckingham [France] ; D. Hilton [Australie] ; A. Nash [Australie] ; T. Mohun [Royaume-Uni] ; R. P. Harvey [Australie]

Source :

RBID : ISTEX:CE5864FFC6882A2B6FD5C75B74215E9730BD5E5D

Descripteurs français

English descriptors

Abstract

Abstract: We report that DAN, a potential cell cycle regulator and tumour suppressor, is a secreted glycoprotein related to Xenopus cerberus. DAN, cerberus, its mouse relative Cer-1/cer-l/Cerberus-like/Cerr1, and the recently described factor DRM/Gremlin, appear to be members of the cystine knot superfamily, which includes TGFβs and BMPs. Like cerberus and mCer-1, DAN induced cement glands as well as markers of anterior neural tissue and endoderm in Xenopus animal cap assays, features of BMP signalling blockade. During mouse embryogenesis, Dan was expressed from E8.5 in cranial mesenchyme and somites, then later in limb and facial mesenchyme. The pattern in somites was highly dynamic, with transcripts initially localized to the caudal half of the nascent epithelial somite, then, after maturation, to sclerotomal cells adjacent to the neural tube. Dan was also expressed in the developing myotome. The expression domains include sites in which BMP inhibition is known to be important for development. Thus, DAN appears to be a secreted factor belonging to the cystine knot superfamily, and one of a growing number of antagonists acting to modulate BMP signalling during development.

Url:
DOI: 10.1016/S0925-4773(98)00139-7


Affiliations:


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Le document en format XML

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<term>Flag peptide</term>
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<term>Hindbrain</term>
<term>Homology</term>
<term>Human norrie disease protein</term>
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<term>Inhibitory effects</term>
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<term>Lateral view</term>
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<term>Medial somite</term>
<term>Medical research</term>
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<term>Muscle progenitor cells</term>
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<term>Nascent somites</term>
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<term>Neural tube</term>
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<term>Nucleic acids</term>
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<term>Rnase protection</term>
<term>Rnase protection analysis</term>
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<term>Ventral domains</term>
<term>Wang</term>
<term>Willebrand factor</term>
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<term>Xenopus animal</term>
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<term>Xenopus cerberus</term>
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<term>Xenopus gene</term>
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<term>Dorsoanterior aspect</term>
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<term>Embryonic development</term>
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<term>Enomoto</term>
<term>Expression vector</term>
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<term>Facial primordia</term>
<term>Flag epitope</term>
<term>Flag peptide</term>
<term>Gene product</term>
<term>Glinka</term>
<term>Head induction</term>
<term>Head mesenchyme</term>
<term>Hindbrain</term>
<term>Homology</term>
<term>Human norrie disease protein</term>
<term>Hybridization</term>
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<term>Inhibitory effects</term>
<term>Kodak eastman</term>
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<term>Lateral mesoderm</term>
<term>Lateral view</term>
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<term>Limb buds</term>
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<term>Muscle progenitor cells</term>
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<term>Nascent somites</term>
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<term>Neural crest</term>
<term>Neural tube</term>
<term>Noggin</term>
<term>Norrie disease</term>
<term>Novel branch</term>
<term>Nucleic acids</term>
<term>Nucleotide sequence</term>
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<term>Ozaki</term>
<term>Patterning</term>
<term>Peptide</term>
<term>Presomitic mesoderm</term>
<term>Protein alignments</term>
<term>Putative</term>
<term>Rnase</term>
<term>Rnase protection</term>
<term>Rnase protection analysis</term>
<term>Sakiyama</term>
<term>Sclerotomal cells</term>
<term>Simultaneous blockade</term>
<term>Somite</term>
<term>Somite patterning</term>
<term>Sonic hedgehog</term>
<term>Spemann organizer</term>
<term>Structural backbone</term>
<term>Superfamily</term>
<term>Tajbakhsh</term>
<term>Tgfb superfamily</term>
<term>Tumour</term>
<term>Tumour suppressor</term>
<term>Ventral</term>
<term>Ventral domains</term>
<term>Wang</term>
<term>Willebrand factor</term>
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<term>Xenopus animal</term>
<term>Xenopus animal caps</term>
<term>Xenopus cerberus</term>
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<term>Xenopus gene</term>
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<div type="abstract" xml:lang="en">Abstract: We report that DAN, a potential cell cycle regulator and tumour suppressor, is a secreted glycoprotein related to Xenopus cerberus. DAN, cerberus, its mouse relative Cer-1/cer-l/Cerberus-like/Cerr1, and the recently described factor DRM/Gremlin, appear to be members of the cystine knot superfamily, which includes TGFβs and BMPs. Like cerberus and mCer-1, DAN induced cement glands as well as markers of anterior neural tissue and endoderm in Xenopus animal cap assays, features of BMP signalling blockade. During mouse embryogenesis, Dan was expressed from E8.5 in cranial mesenchyme and somites, then later in limb and facial mesenchyme. The pattern in somites was highly dynamic, with transcripts initially localized to the caudal half of the nascent epithelial somite, then, after maturation, to sclerotomal cells adjacent to the neural tube. Dan was also expressed in the developing myotome. The expression domains include sites in which BMP inhibition is known to be important for development. Thus, DAN appears to be a secreted factor belonging to the cystine knot superfamily, and one of a growing number of antagonists acting to modulate BMP signalling during development.</div>
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