The transcriptional coactivator FHL2 transmits Rho signals from the cell membrane into the nucleus

被引:161
作者
Müller, JM
Metzger, E
Greschik, H
Bosserhoff, AK
Mercep, L
Buettner, R
Schüle, R
机构
[1] Univ Freiburg, Frauenklin, D-79106 Freiburg, Germany
[2] Univ Freiburg Klinikum, Zentrum Klin Forsch, D-79106 Freiburg, Germany
[3] Rhein Westfal TH Aachen Klinikum, Inst Pathol, D-52074 Aachen, Germany
[4] Univ Klinikum Bonn, Inst Pathol, D-53127 Bonn, Germany
关键词
androgen receptor; FHL2; nuclear translocation; small GTPases; transcriptional coactivator;
D O I
10.1093/emboj/21.4.736
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
GTPases of the Rho family are transducers of extracellular signals and control cellular processes such as organization of the actin cytoskeleton, motility, adhesion and gene regulation. The Rho signalling pathway is activated, for example, by bioactive sphingolipids such as sphingosine-1-phosphate (SPP) or by overexpression of Rho family members in tumorigenesis and metastases. Here, we show that stimulation of the Rho signalling pathway induces translocation of the transcriptional LIM-only coactivator FHL2 to the nucleus and subsequent activation of FHL2- and androgen receptor-dependent genes. Interestingly, prostate tumours overexpress Rho GTPases and display altered cellular localization of FHL2 concomitant with tumour dedifferentiation. SPP-induced FHL2 activation is mediated by Rho GTPases, but not by the GTPases Cdc42, Rac1 or Ras, and depends on Rhokinase. In addition, Rho signalling influences other transcriptional coactivators, thus pointing to a general regulatory role for Rho GTPases in cofactor function. In summary, our data propose a yet undescribed signalling pathway in which the coactivator FHL2 acts as a novel molecular transmitter of the Rho signalling pathway, thereby integrating extracellular cues into altered gene expression.
引用
收藏
页码:736 / 748
页数:13
相关论文
共 49 条
[1]   Activation of RhoA and SAPK/JNK signalling pathways by the RhoA-specific exchange factor mNET1 [J].
Alberts, AS ;
Treisman, R .
EMBO JOURNAL, 1998, 17 (14) :4075-4085
[2]   The LIM domain: regulation by association [J].
Bach, I .
MECHANISMS OF DEVELOPMENT, 2000, 91 (1-2) :5-17
[3]   Ras and Rho GTPases: A family reunion [J].
Bar-Sagi, D ;
Hall, A .
CELL, 2000, 103 (02) :227-238
[4]   Rho GTPases and their effector proteins [J].
Bishop, AL ;
Hall, A .
BIOCHEMICAL JOURNAL, 2000, 348 (02) :241-255
[5]   Microbial toxins and the glycosylation of Rho family GTPases [J].
Busch, C ;
Aktories, K .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2000, 10 (05) :528-535
[6]   The Dbl family of oncogenes [J].
Cerione, RA ;
Zheng, Y .
CURRENT OPINION IN CELL BIOLOGY, 1996, 8 (02) :216-222
[7]   Molecular cloning and characterization of FHL2, a novel LIM domain protein preferentially expressed in human heart [J].
Chan, KK ;
Tsui, SKW ;
Lee, SMY ;
Luk, SCW ;
Liew, CC ;
Fung, KP ;
Waye, MMY ;
Lee, CY .
GENE, 1998, 210 (02) :345-350
[8]   Tissue-specific GATA factors are transcriptional effectors of the small GTPase RhoA [J].
Charron, F ;
Tsimiklis, G ;
Areand, M ;
Robitaille, L ;
Liang, QR ;
Molkentin, JD ;
Meloche, S ;
Nemer, M .
GENES & DEVELOPMENT, 2001, 15 (20) :2702-2719
[9]   Regulation of c-myc expression by PDGF through Rho GTPases [J].
Chiariello, M ;
Marinissen, MJ ;
Gutkind, JS .
NATURE CELL BIOLOGY, 2001, 3 (06) :580-586
[10]   Genomic analysis of metastasis reveals an essential role for RhoC [J].
Clark, EA ;
Golub, TR ;
Lander, ES ;
Hynes, RO .
NATURE, 2000, 406 (6795) :532-535