The role of TCL1 in human T-cell leukemia

被引:72
作者
Pekarsky, Y [1 ]
Hallas, C [1 ]
Croce, CM [1 ]
机构
[1] Thomas Jefferson Univ, Kimmerl Canc Ctr, Philadelphia, PA 19107 USA
关键词
14q32.1; TCLI; TCLIb; Akt; T-cell leukemia;
D O I
10.1038/sj.onc.1204596
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
The TCL1 locus on human chromosome 14q32.1 is activated in T-cell leukemias by translocations and inversions that juxtapose it to regulatory elements of T-cell receptor genes. We isolated and characterized four genes at this locus, TCL1 and TCL1b (T-cell leukemia/lymphoma 1 and 1b), and TNG1 and TNG2 (TCL neighboring genes 1 and 2) all of which are overexpressed following rearrangements involving 14q32.1. TCL1 and TCL1b show 60% similarity and are represented in the mouse by a cluster of six homologous genes. In humans TCL1 and TCL1b show similar expression patterns: They are expressed mainly in CD4-/CD8- immature T-cells, pre B-cells and virgin B-cells. Expression decreases significantly at more mature stages of B-cell development. Activation of TCL1 and/or TCL1b in mature T-cells causes T-cell leukemia in humans. The oncogenic nature of TCL1 was confirmed by the analysis of a transgenic mouse model. Functional analysis of Tcl1 revealed its involvement in a P13-kinase dependent Akt (PKB) pro-survival pathway through its interaction with the Akt kinase which increases Akt's enzymatic activity and promotes translocation of Akt to the nucleus.
引用
收藏
页码:5638 / 5643
页数:6
相关论文
共 43 条
[1]   Chromosomal imbalances in adult T-cell leukemia revealed by comparative genomic hybridization: gains at 14q32 and 2p16-22 in cell lines [J].
Ariyama, Y ;
Mori, T ;
Shinomiya, T ;
Sakabe, T ;
Fukuda, Y ;
Kanamaru, A ;
Yamada, Y ;
Isobe, M ;
Seto, M ;
Nakamura, Y ;
Inazawa, J .
JOURNAL OF HUMAN GENETICS, 1999, 44 (06) :357-363
[2]   DIFFERENTIAL EXPRESSION OF THE TRANSLOCATED AND THE UNTRANSLOCATED C-MYC ONCOGENE IN BURKITT-LYMPHOMA [J].
ARRUSHDI, A ;
NISHIKURA, K ;
ERIKSON, J ;
WATT, R ;
ROVERA, G ;
CROCE, CM .
SCIENCE, 1983, 222 (4622) :390-393
[3]   INVERSIONS AND TANDEM TRANSLOCATIONS INVOLVING CHROMOSOME 14Q11 AND 14Q32 IN T-PROLYMPHOCYTIC LEUKEMIA AND T-CELL LEUKEMIAS IN PATIENTS WITH ATAXIA TELANGIECTASIA [J].
BRITOBABAPULLE, V ;
CATOVSKY, D .
CANCER GENETICS AND CYTOGENETICS, 1991, 55 (01) :1-9
[4]   AKT/PKB and other D3 phosphoinositide-regulated kinases: Kinase activation by phosphoinositide-dependent phosphorylation [J].
Chan, TO ;
Rittenhouse, SE ;
Tsichlis, PN .
ANNUAL REVIEW OF BIOCHEMISTRY, 1999, 68 :965-1014
[5]   Functional redundancy of the Nur77 and Nor-1 orphan steroid receptors in T-cell apoptosis [J].
Cheng, LEC ;
Chan, FKM ;
Cado, D ;
Winoto, A .
EMBO JOURNAL, 1997, 16 (08) :1865-1875
[6]  
CIMINO G, 1991, CANCER RES, V51, P6712
[7]   An MII-AF9 fusion gene made by homologous recombination causes acute leukemia in chimeric mice: A method to create fusion oncogenes [J].
Corral, J ;
Lavenir, I ;
Impey, H ;
Warren, AJ ;
Forster, A ;
Larson, TA ;
Bell, S ;
McKenzie, ANJ ;
King, G ;
Rabbitts, TH .
CELL, 1996, 85 (06) :853-861
[8]  
Croce CM, 1999, CANCER RES, V59, p1778S
[9]   GENE FOR ALPHA-CHAIN OF HUMAN T-CELL RECEPTOR - LOCATION ON CHROMOSOME-14 REGION INVOLVED IN T-CELL NEOPLASMS [J].
CROCE, CM ;
ISOBE, M ;
PALUMBO, A ;
PUCK, J ;
MING, J ;
TWEARDY, D ;
ERIKSON, J ;
DAVIS, M ;
ROVERA, G .
SCIENCE, 1985, 227 (4690) :1044-1047
[10]   ROLE OF CHROMOSOME TRANSLOCATIONS IN HUMAN NEOPLASIA [J].
CROCE, CM .
CELL, 1987, 49 (02) :155-156