Cloning and functional characterization of a new Ski homolog, Fussel-18, specifically expressed in neuronal tissues

被引:31
作者
Arndt, S
Poser, I
Schubert, T
Moser, M
Bosserhoff, AK
机构
[1] Univ Regensburg, Inst Pathol, Sch Med, D-93053 Regensburg, Germany
[2] Max Planck Inst Biochem, D-82152 Martinsried, Germany
关键词
cerebellum; transforming growth factor; inhibitor; ski family; Smad; signaling;
D O I
10.1038/labinvest.3700344
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The Sloan Kettering Virus ( Ski) family of nuclear oncoproteins represses transforming growth factor-beta (TGF-beta) signaling through inhibition of transcriptional activity of Smad proteins. Here, we report the discovery of a new functional Smad suppressing element on chromosome 18 (Fussel-18). Fussel-18 encodes for a protein of 297 amino acids sharing characteristic structural features, significant homology and similar genomic organization with the homolog Ski family members, Ski and Ski-related novel sequence (Sno). In contrast to Ski and Sno, which are ubiquitously expressed in human tissues, in situ hybridization, RT-PCR, Western blot and immunohistochemistry revealed a highly specific expression pattern for Fussel-18 in neuronal tissues, especially in the cerebellum, the spinal cord and dorsal root ganglia, during both embryogenesis and adult stage. Functionally, we determined interaction of Fussel-18 with Smad 2 and Smad 3 together with an inhibitory activity on TGF-beta signaling. Fussel-18 is the first example of a Smad-binding protein with a highly restricted expression pattern within the nervous system.
引用
收藏
页码:1330 / 1341
页数:12
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