Identification of DRG family regulatory proteins (DFRPs): specific regulation of DRG1 and DRG2

被引:44
|
作者
Ishikawa, K
Azuma, S
Ikawa, S
Semba, K
Inoue, J
机构
[1] Univ Tokyo, Inst Med Sci, Dept Canc Biol, Div Cellular & Mol Biol,Minato Ku, Tokyo 1088639, Japan
[2] Tohoku Univ, Inst Dev Ageing & Canc, Dept Cell Biol, Aoba Ku, Sendai, Miyagi 9808575, Japan
关键词
D O I
10.1111/j.1365-2443.2005.00825.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
DRG1 and DRG2 comprise a highly conserved subfamily of GTP-binding proteins and are thought to act as critical regulators of cell growth. Their abnormal expressions may trigger cell transformation or cell cycle arrest. Our aim is to clarify their physiological functions and regulatory mechanisms. Here we report identification of novel proteins, DRG family regulatory protein (DFRP) 1 and DFRP2, which regulate expression of DRG proteins through specific binding. In transient transfection experiments, DFRP1 specifically binds DRG1, and DFRP2 preferentially binds DRG2. DFRPs provide stability to the target DRG proteins through physical association, possibly by blocking the poly-ubiquitination that would precede proteolysis of DRG proteins. DFRPs are highly conserved in eucaryotes, and the expression patterns of dfrp1 and drg1 transcripts in Xenopus embryos and tissues are similar, indicating that these genes work cooperatively in various types of eukaryotic cells. Immunofluorescence experiments have revealed that the interaction between DRG1 and DFRP1 may occur in the cytoplasm. We generated dfrp1- knockout cells and found that endogenous expression of DRG1 is regulated by DFRP1, confirming that DFRP1 is a specific up-regulator of DRG1 in vivo. On the basis of these results, we propose that DRG1 and DRG2 are regulated differently despite their structural similarities.
引用
收藏
页码:139 / 150
页数:12
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