Transformation of Ba/F3 cells and rat-1 cells by ETV6/ARG

被引:17
作者
Iijima, Y
Okuda, K
Tojo, A
Tri, NK
Setoyama, M
Sakaki, Y
Asano, S
Tokunaga, K
Kruh, GD
Sato, Y
机构
[1] Int Med Ctr Japan, Res Inst, Dept Clin Pathol, Div Mol Cytogenet,Shinjuku Ku, Tokyo 1620052, Japan
[2] Kyoto Prefectural Univ Med, Dept Hyg, Kyoto 6020841, Japan
[3] Univ Tokyo, Inst Med Sci, Adv Clin Res Ctr, Div Mol Therapy, Tokyo 1088639, Japan
[4] Univ Tokyo, Inst Med Sci, Ctr Human Genome, Lab Funct Genomics, Tokyo 1088639, Japan
[5] Univ Tokyo, Grad Sch Med, Sch Int Hlth, Dept Human Genet, Tokyo 1130033, Japan
[6] Fox Chase Canc Ctr, Div Med Sci, Philadelphia, PA 19111 USA
关键词
translocation; tyrosine kinase; ETV6/ARG; transforming activity;
D O I
10.1038/sj.onc.1205544
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
ETV6/ARG, a novel fusion gene composed of the ETV6 HLH oligomerization domain and most of sequences of the ARG protein tyrosine, was recently identified in human leukemia cells. The presence of the ETV6/ARG translocation raises the possibility that the resulting fusion protein functions as an oncogene. However, the transforming activity of the ETV6/ARG protein has not been determined and its contribution to leukemogenesis is therefore unknown. Here we address this question by analysing the oncogenic activity of ETV6/ARG in hematopoietic and fibroblast cells. It is demonstrated that expression of ETV6/ARG confers IL3-independent growth to Ba/F3 cells and anchorage independent growth to Rat-1 fibroblasts. It is also shown that multiple signaling molecules, including PI3K, SHC, ras-GAP and CRK-L, are tyrosine phosphorylated in Ba/F3 cells that express ETV6/ARG. Analysis of four different types of ETV6/ARG transcripts previously identified in the AML-M3 leukemia cell line HT93A suggest that ETV6 HLH domain is required for oncogenic activity. Based upon these results it is concluded that ARG can be activated as an oncogene in human malignancy and that the ETV6/ARG oncoprotein triggers some of the same signaling pathways associated with activated ABL oncogenes.
引用
收藏
页码:4374 / 4383
页数:10
相关论文
共 23 条
[1]  
Andreasson P, 1997, GENE CHROMOSOME CANC, V20, P299
[2]   Tyrosine phosphorylation of RNA polymerase II carboxyl-terminal domain by the Abl-related gene product [J].
Baskaran, R ;
Chiang, GG ;
Mysliwiec, T ;
Kruh, GD ;
Wang, JYJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (30) :18905-18909
[3]   The TEL platelet-derived growth factor beta receptor (PDGF beta R) fusion in chronic myelomonocytic leukemia is a transforming protein that self-associates and activates PDGF beta R kinase-dependent signaling pathways [J].
Carroll, M ;
Tomasson, MH ;
Barker, GF ;
Golub, TR ;
Gilliland, DG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14845-14850
[4]   The tyrosine kinase Abl-related gene ARG is fused to ETV6 in an AML-M4Eo patient with a t(1;12)(q25;p13):: Molecular cloning of both reciprocal transcripts [J].
Cazzaniga, G ;
Tosi, S ;
Aloisi, A ;
Giudici, G ;
Daniotti, M ;
Pioltelli, P ;
Kearney, L ;
Biondi, A .
BLOOD, 1999, 94 (12) :4370-4373
[5]   FUSION OF PDGF RECEPTOR-BETA TO A NOVEL ETS-LIKE GENE, TEL, IN CHRONIC MYELOMONOCYTIC LEUKEMIA WITH T(512) CHROMOSOMAL TRANSLOCATION [J].
GOLUB, TR ;
BARKER, GF ;
LOVETT, M ;
GILLILAND, DG .
CELL, 1994, 77 (02) :307-316
[6]  
Golub TR, 1996, MOL CELL BIOL, V16, P4107
[7]  
Iijima Y, 2000, BLOOD, V95, P2126
[8]   A novel ETV6-NTRK3 gene fusion in congenital fibrosarcoma [J].
Knezevich, SR ;
McFadden, DE ;
Tao, W ;
Lim, JF ;
Sorensen, PHB .
NATURE GENETICS, 1998, 18 (02) :184-187
[9]   THE COMPLETE CODING SEQUENCE OF ARG DEFINES THE ABELSON SUBFAMILY OF CYTOPLASMIC TYROSINE KINASES [J].
KRUH, GD ;
PEREGO, R ;
MIKI, T ;
AARONSON, SA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (15) :5802-5806
[10]   A TEL-JAK2 fusion protein with constitutive kinase activity in human leukemia [J].
Lacronique, V ;
Boureux, A ;
DellaValle, V ;
Poirel, H ;
Quang, CT ;
Mauchauffe, M ;
Berthou, C ;
Lessard, M ;
Berger, R ;
Ghysdael, J ;
Bernard, OA .
SCIENCE, 1997, 278 (5341) :1309-1312