Rat neuronal leucine-rich repeat protein-3: Cloning and regulation of the gene expression

被引:20
作者
Fukamachi, K
Matsuoka, Y
Kitanaka, C
Kuchino, Y
Tsuda, H
机构
[1] Natl Canc Ctr, Res Inst, Expt Pathol & Chemotherapy Div, Chuo Ku, Tokyo 1040045, Japan
[2] Natl Canc Ctr, Res Inst, Div Biophys, Chuo Ku, Tokyo 1040045, Japan
关键词
Ras; mitogen-activated protein kinase; MAPK/ERK kinase; leucine-rich repeat protein; cell adhesion; clathrin;
D O I
10.1006/bbrc.2001.5579
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
Rat neuronal leucine-rich repeat protein-3 (rNLRR-3) gene was isolated and cloned from fibrosarcoma cells overexpressing c-Ha-ras. Stable expression of constitutively active forms of Ras (H-Ras(V12) or v-H-Ras) led to a two- to fourfold increase in rNLRR-3 mRNA in rat normal fibroblasts (3Y1). When cells expressing H-Ras(V12) were treated with mitogen activated protein kinase (MAPK) kinase inhibitors (U0126, PD98059), suppression of rNLRR-3 mRNA correlated well with a reduction in MAPK activity. Epidermal growth factor (EGF) led to elevation of rNLRR-3 gene expression about 4 h after stimulation of normal fibroblasts. U0126 completely suppressed the induction by EGF of rNLRR-3 mRNA with abrogation of MAPK phosphorylation. U0126 inhibited the basal transcription of rNLRR-3. LY294002, a PI3 kinase inhibitor, showed a lesser effect on expression of the gene. These results indicate that rNLRR-3 gene expression is regulated mainly through the Ras-MAPK signaling pathway in fibroblasts. (C) 2001 Academic Press.
引用
收藏
页码:257 / 263
页数:7
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