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Getting a first clue about SPRED functions
被引:86
作者:

Bundschu, Karin
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机构: Univ Ulm, Abt Biochem & Mol Biol, D-89081 Ulm, Germany

Walter, Ulrich
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机构: Univ Ulm, Abt Biochem & Mol Biol, D-89081 Ulm, Germany

Schuh, Kai
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机构: Univ Ulm, Abt Biochem & Mol Biol, D-89081 Ulm, Germany
机构:
[1] Univ Ulm, Abt Biochem & Mol Biol, D-89081 Ulm, Germany
[2] Inst Klin Biochem & Pathobiochem, Wurzburg, Germany
[3] Univ Wurzburg, Inst Physiol, D-97070 Wurzburg, Germany
来源:
关键词:
D O I:
10.1002/bies.20632
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Spreds form a new protein family with an N-terminal Enabled/VASP homology 1 domain (EVH1), a central c-Kit binding domain (KBD) and a C-terminal Sprouty-related domain (SPR). They are able to inhibit the Ras-ERK signalling pathway after various mitogenic stimulations. In mice, Spired proteins are identified as regulators of bone morphogenesis, hematopoietic processes, allergen-induced airway eosinophilia and hyperresponsiveness. They inhibit cell motility and metastasis and have a high potential as tumor markers and suppressors of carcinogenesis. Moreover, in vertebrates, XtSpreds help together with XtSprouty proteins to coordinate gastrulation and mesoderm specification. Here, we give an overview of this new field and summarize the domain functions, binding partners, expression patterns and the cellular localizations, regulations and functions of Spired proteins and try to give perspectives for future scientific directions.
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页码:897 / 907
页数:11
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