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Growth/Differentiation Factor-10: A New Member of the Transforming Growth Factor-βSuperfamily Related to Bone Morphogenetic Protein-3

 

作者: CunninghamNoreen S.,   JenkinsNancy A.,   GilbertDebra J.,   CopelandNeal G.,   ReddiA. Hari,   JinSe,  

 

期刊: Growth Factors  (Taylor Available online 1995)
卷期: Volume 12, issue 2  

页码: 99-109

 

ISSN:0897-7194

 

年代: 1995

 

DOI:10.3109/08977199509028956

 

出版商: Taylor&Francis

 

关键词: growth/differentiation factor;bone morphogenetic protein-3

 

数据来源: Taylor

 

摘要:

AbstractWe have identified a new member of the transforming growth factor-β(TGF-β) superfamily, growth/differentiation factor-10 (GDF-10), which is highly related to bone morphogenetic protein-3 (BMP-3). The nucleotide sequence of GDF-10 encodes a predicted protein of 476 amino acids with a molecular weight of approximately 52,000. The GDF-10 polypeptide contains a potential signal sequence for secretion, a putative RXXR proteolytic processing site, and a carboxy-terminal domain with considerable homology to other known members of the TGF-βsuperfamily. In the mature carboxy-terminal domain GDF-10 is more homologous to BMP-3 (83% amino acid sequence identity) than to any other previously identified TGF-βfamily member. GDF-10 also shows significant homology to BMP-3 (approximately 30% amino acid sequence identity) in the pro-region of the molecule. Based on these sequence comparisons, GDF-10 and BMP-3 define a new subgroup within the larger TGF-βsuperfamily. By Northern analysis, GDF-10 mRNA was detected primarily in murine uterus, adipose tissue, and brain and to a lesser extent in liver and spleen. In addition, GDF-10 mRNA was present in both neonatal and adult bone samples, with higher levels being detected in calvaria than in long bone. These results suggest that GDF10 may play multiple roles in regulating cell differentiation events, including those involved in skeletal morphogenesis. Gdf10 was mapped to the proximal region of mouse chromosome 14 close to a region known to contain a spontaneous recessive mutation that is associated with a craniofacial defect.

 

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