The gene for a new brain specific RhoA exchange factor maps to the highly unstable chromosomal region 1p36.2-1p36.3.

被引:39
作者
De Toledo, M
Coulon, V
Schmidt, S
Fort, P
Blangy, A
机构
[1] Ctr Rech Biochim Macromol, CNRS IFR24 UPR 1086, F-34293 Montpellier 5, France
[2] Inst Genet Mol Montpellier, CNRS IFR24 UMR 5535, F-34293 Montpellier 5, France
关键词
Rho GTPase; Dbl exchange factor; transformation; 1p36; chromosome; 1;
D O I
10.1038/sj.onc.1204921
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
Guanine nucleotide exchange factors from the Dbl family are proto-oncogenic proteins that activate small GTPases of the Rho family. Here we report the characterization of GEF720, a novel Dbl-like protein related to p115Rho-GEF. GEF720 activated RhoA both in our recently developed Yeast Exchange Assay and in biochemical in vitro exchange assays. GEF720 induced RhoA dependent assembly of actin stress fibers in REF52 fibroblastic cells. In NIH3T3 cells this Dbl-like protein elicited formation of transformation foci with a morphology similar to RhoA-V14 induced foci. In the PC12 neuron-like cell line, expression of GEF720, whose mRNA is brain specific, inhibited NGF-induced neurite outgrowth. Finally, GEF720 gene is located on human chromosome 1 on band 1p36, between Tumor Protein 73 and Tumor Necrosis Factor Receptor 12, two genes rearranged in many neuroblastoma cell lines. Together, these results show that this new Dbl related protein, GEF720, is an exchange factor that can directly activate RhoA in vivo and is potentially involved in the control of neuronal cell differentiation. GEF720 is also a new candidate gene involved in the progression of neuroblastoma and developmental abnormalities associated with rearrangements in the 1p36 chromosomal region.
引用
收藏
页码:7307 / 7317
页数:11
相关论文
共 70 条
[1]   Structure and mutagenesis of the Dbl homology domain [J].
Aghazadeh, B ;
Zhu, K ;
Kubiseski, TJ ;
Liu, GA ;
Pawson, T ;
Zheng, Y ;
Rosen, MK .
NATURE STRUCTURAL BIOLOGY, 1998, 5 (12) :1098-1107
[2]   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
[3]   Analysis of RhoA-binding proteins reveals an interaction domain conserved in heterotrimeric G protein β subunits and the yeast response regulator protein Skn7 [J].
Alberts, AS ;
Bouquin, N ;
Johnston, LH ;
Treisman, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (15) :8616-8622
[4]  
Åman AK, 2000, GENE CHROMOSOME CANC, V29, P292, DOI 10.1002/1098-2264(2000)9999:9999<::AID-GCC1038>3.0.CO
[5]  
2-C
[6]   Identification and characterization of novel genes located at the t(1;15)(p36.2;q24) translocation breakpoint in the neuroblastoma cell line NGP [J].
Amler, LC ;
Bauer, A ;
Corvi, R ;
Dihlmann, S ;
Praml, C ;
Cavenee, WK ;
Schwab, M ;
Hampton, GM .
GENOMICS, 2000, 64 (02) :195-202
[7]   Chp, a homologue of the GTPase Cdc42Hs, activates the JNK pathway and is implicated in reorganizing the actin cytoskeleton [J].
Aronheim, A ;
Broder, YC ;
Cohen, A ;
Fritsch, A ;
Belisle, B ;
Abo, A .
CURRENT BIOLOGY, 1998, 8 (20) :1125-1128
[8]   The two guanine nucleotide exchange factor domains of Trio link the Rac1 and the RhoA pathways in vivo [J].
Bellanger, JM ;
Lazaro, JB ;
Diriong, S ;
Fernandez, A ;
Lamb, N ;
Debant, A .
ONCOGENE, 1998, 16 (02) :147-152
[9]  
Blangy A, 2000, J CELL SCI, V113, P729
[10]   Identification and characterization of a novel Rho-specific guanine nucleotide exchange factor [J].
Blomquist, A ;
Schwörer, G ;
Schablowski, H ;
Psoma, A ;
Lehnen, M ;
Jakobs, KH ;
Rümenapp, U .
BIOCHEMICAL JOURNAL, 2000, 352 :319-325