Document Detail


Distinct spatial and temporal expression patterns of two type I receptors for bone morphogenetic proteins during mouse embryogenesis.
MedLine Citation:
PMID:  7750489     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Bone morphogenetic proteins (BMPs) are multifunctional proteins structurally related to transforming growth factor-beta (TGF beta) and activin that can induce cartilage and bone growth in vivo. Members of the TGF beta superfamily exert their biological effects via heteromeric serine/threonine kinase complexes of type I and type II receptors. We previously obtained six different type I receptors, termed activin receptor-like kinase-1 (ALK-1) to -6. ALK-5 is a TGF beta type I receptor, ALK-2 and ALK-4 are activin type I receptors, and ALK-3 and ALK-6 are type I receptors for osteogenic protein-1 (OP-1)/bone morphogenetic protein-7 (BMP-7) and BMP-4. Here we report the complementary DNA cloning of the mouse homolog of ALK-3, which is highly conserved between mouse and man. ALK-3 messenger RNA (mRNA) is ubiquitously expressed in various adult mouse tissues, whereas ALK-6 mRNA is only found in brain and lung. The distribution of ALK-3 and ALK-6 mRNA in the postimplantation mouse embryo [6.5-15.5 days postcoitum (pc)] was studied by in situ hybridization. ALK-3 was nearly ubiquitously expressed throughout these stages of development, but was notably absent in the liver. In contrast, ALK-6 showed a more restricted expression pattern. ALK-6 mRNA was absent in early postimplantation embryos, was detected first in 9.5 days pc embryos, and persisted until 15.5 days pc. In midgestation embryos, ALK-6 transcripts were detected in mesenchymal precartilage condensations, premuscle masses, blood vessels, central nervous system, parts of the developing ear and eye, and epithelium. The expression in sites of developing cartilage and bone supports the idea that ALK-3 and -6 are receptors for BMPs in vivo. In addition, the expression of these genes in many soft tissues suggests broader functions for BMPs in embryogenesis.
Authors:
N Dewulf; K Verschueren; O Lonnoy; A Morén; S Grimsby; K Vande Spiegle; K Miyazono; D Huylebroeck; P Ten Dijke
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Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Endocrinology     Volume:  136     ISSN:  0013-7227     ISO Abbreviation:  Endocrinology     Publication Date:  1995 Jun 
Date Detail:
Created Date:  1995-06-19     Completed Date:  1995-06-19     Revised Date:  2012-06-25    
Medline Journal Info:
Nlm Unique ID:  0375040     Medline TA:  Endocrinology     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  2652-63     Citation Subset:  AIM; IM    
Affiliation:
Laboratory of Molecular Biology (CELGEN), University of Leuven, Belgium.
Data Bank Information
Bank Name/Acc. No.:
GENBANK/L48015;  Z23154;  Z31664
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MeSH Terms
Descriptor/Qualifier:
Activin Receptors
Amino Acid Sequence
Animals
Bone Morphogenetic Protein Receptors
Bone Morphogenetic Protein Receptors, Type I
Cloning, Molecular
Embryonic and Fetal Development / genetics
Gene Expression Regulation, Developmental
Humans
Mice
Molecular Sequence Data
Protein-Serine-Threonine Kinases / classification,  genetics*
RNA, Messenger / genetics,  metabolism
Receptors, Cell Surface / classification,  genetics*
Receptors, Growth Factor*
Sequence Homology, Amino Acid
Tissue Distribution
Chemical
Reg. No./Substance:
0/RNA, Messenger; 0/Receptors, Cell Surface; 0/Receptors, Growth Factor; EC 2.7.11.1/Protein-Serine-Threonine Kinases; EC 2.7.11.30/Activin Receptors; EC 2.7.11.30/Bmpr1a protein, mouse; EC 2.7.11.30/Bone Morphogenetic Protein Receptors; EC 2.7.11.30/Bone Morphogenetic Protein Receptors, Type I

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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