期刊文章详细信息
Review of current progress in the structure and function of Smad proteins ( SCI收录)
Review of current progress in the structure and function of Smad proteins
文献类型:期刊文章
机构地区:[1]解放军第304医院全军创伤修复重点研究室,北京100037
基 金:supported by a grant from the National Natural Science Foundation of China(No.G1999054204); the National Prominent Youth Science Foundation of China(No.39525024).
年 份:2002
期 号:3
起止页码:446-450
语 种:中文
收录情况:BIOSISPREVIEWS、CAB、CAS、CSA-PROQEUST、CSCD、CSCD2011_2012、DOAJ、EBSCO、EMBASE、IC、JST、PROQUEST、PUBMED、SCI(收录号:WOS:000174717800032)、SCI-EXPANDED(收录号:WOS:000174717800032)、SCIE、SCOPUS、WOS、ZGKJHX、普通刊
摘 要:PURPOSE: To review the recent developments in the structure and function of Smad proteins. DATA SOURCES: Both Chinese- and English-language literatures were searched using MEDLINE/CD-ROM (1997 - 2000) and the Index of Chinese-Language Literature (1997 - 2000). STUDY SELECTION: Data from published articles about TGF-beta signal transduction in recent domestic and foreign literature were selected. DATA EXTRACTION: Data were mainly extracted from 22 articles which are listed in the reference section of this review. RESULTS: Smad proteins mediate signal transduction induced by the TGF-beta superfamily. Based on their structural and functional properties, Smad proteins are divided into three groups. The first group, receptor-regulated Smads (R-Smads), are phosphorylated by activated type I receptors and form heteromeric complexes with the second group of Smads, common mediator Smads (Co-Smads). These Smad complexes translocate into the nucleus to influence gene transcription. Inhibitory Smads (I-Smads) are the third group and these antagonize the activity of R-Smads. In the nucleus, Smads can directly contact Smad-binding elements (SBE) in target gene promoters. Through interaction with different transcription factors, transcriptional co-activators or co-repressors, Smads elicit different effects in various cell types. The aberrance of Smad proteins has been noted in several human disorders such as fibrosis, hypertrophic scarring and cancer. CONCLUSION: The structure of Smads determines their function as transcriptional factors which translocate signals from the cell surface to the nucleus where Smads regulate TGF-beta superfamily-dependent gene expression.
关 键 词:DNA-Binding Proteins Humans Research Support, Non-U.S. Gov't Signal Transduction Smad Proteins TRANS-ACTIVATORS Transcription Factors Transforming Growth Factor beta
分 类 号:R341[基础医学类]
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