AN RNA-BINDING PROTEIN GENE, TLS/FUS, IS FUSED TO ERG IN HUMAN MYELOID-LEUKEMIA WITH T(16,21) CHROMOSOMAL TRANSLOCATION

被引:1
|
作者
ICHIKAWA, H [1 ]
SHIMIZU, K [1 ]
HAYASHI, Y [1 ]
OHKI, M [1 ]
机构
[1] UNIV TOKYO,FAC MED,DEPT PEDIAT,BUNKYO KU,TOKYO 113,JAPAN
关键词
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The t(16;21)(p11;q22) translocation is a recurrent chromosomal abnormality found in several types of myeloid leukemia. We have previously demonstrated that the breakpoints of this translocation are clustered in a specific intron of the ERG gene on chromosome 21, which has recently been reported to be involved in Ewing's sarcoma. We show here that the TLS/FUS gene on chromosome 16 is fused with the ERG gene to produce the TLS/FUS-ERG chimeric transcript by this translocation. The TLS/FUS gene has been identified as a translocated gene in myxoid liposarcoma by the t(12;16)(q13;p11) translocation and encodes an RNA-binding protein that is highly homologous to the product of the EWS gene involved in Ewing's sarcoma. Thus, the TLS/FUS-ERG gene fusion in t(16;21) leukemia is predicted to produce a protein that is very similar to the EWS-ERG chimeric protein responsible for Ewing's sarcoma.
引用
收藏
页码:2865 / 2868
页数:4
相关论文
共 42 条
  • [21] CABEZA, A DROSOPHILA GENE ENCODING A NOVEL RNA-BINDING PROTEIN, SHARES HOMOLOGY WITH EWS AND TLS, 2 GENES INVOLVED IN HUMAN SARCOMA FORMATION
    STOLOW, DT
    HAYNES, SR
    NUCLEIC ACIDS RESEARCH, 1995, 23 (05) : 835 - 843
  • [22] The RTK-RAS signaling pathway is enriched in patients with rare acute myeloid leukemia harboring t(16;21)(p11;q22)/FUS::ERG
    Lai, Anli
    Liu, Wenbing
    Wei, Hui
    Wang, Ying
    Lin, Dong
    Zhou, Chunlin
    Liu, Bingcheng
    Gu, Runxia
    Li, Yan
    Wei, Shuning
    Gong, Benfa
    Liu, Kaiqi
    Gong, Xiaoyuan
    Liu, Yuntao
    Zhang, Guangji
    Zhang, Junping
    Mi, Yingchang
    Wang, Jianxiang
    Qiu, Shaowei
    BLOOD SCIENCE, 2024, 6 (02):
  • [23] TLSI/FUS-ERG fusion gene in acute lymphoblastic leukemia with t(16;21)(p11;q22) and monitoring of minimal residual disease
    Kanazawa, T
    Ogawa, C
    Taketani, T
    Taki, T
    Hayashi, Y
    Morikawa, A
    LEUKEMIA & LYMPHOMA, 2005, 46 (12) : 1833 - 1835
  • [24] A novel gene, MSI2, encoding a putative RNA-binding protein is recurrently rearranged at disease progression of chronic myeloid leukemia.
    Barbouti, A
    Höglund, M
    Johansson, B
    Lassen, C
    Nilsson, PG
    Winquist, I
    Hagemeijer, A
    Mitelman, F
    Fioretos, T
    BLOOD, 2002, 100 (11) : 529A - 529A
  • [25] IFI-16 GENE ENCODES A NUCLEAR-PROTEIN WHOSE EXPRESSION IS INDUCED BY INTERFERONS IN HUMAN MYELOID-LEUKEMIA CELL-LINES
    DAWSON, MJ
    TRAPANI, JA
    JOURNAL OF CELLULAR BIOCHEMISTRY, 1995, 57 (01) : 39 - 51
  • [26] The Unfolded Protein Response (UPR) Is Activated in Human Acute Myeloid Leukemia (AML) and Suppresses Translation of the CCAAT/Enhancer Binding Protein-Alpha (CEBPA) by Induction of the RNA-Binding Protein Calreticulin
    Schardt, Julian
    Eyholzer, Marianne
    Mueller, Beatrice U.
    Pabst, Thomas
    BLOOD, 2008, 112 (11) : 1009 - 1009
  • [27] Identification of a Potential "Hotspot" DNA Region in the RUNXI Gene Targeted by Mitoxantrone in Therapy-Related Acute Myeloid Leukemia with t(16;21) Translocation
    Ottone, Tiziana
    Hasan, Syed Khizer
    Montefusco, Enrico
    Curzi, Paola
    Mays, Ashley N.
    Chessa, Luciana
    Ferrari, Antonella
    Conte, Esmeralda
    Noguera, Nelida Ines
    Lavorgna, Serena
    Ammatuna, Emanuele
    Divona, Mariadomenica
    Bovetti, Katia
    Annadori, Sergio
    Grimwade, David
    Lo-Coco, Francesco
    GENES CHROMOSOMES & CANCER, 2009, 48 (03): : 213 - 221
  • [28] Establishment and characterization of a novel acute myeloid leukemia cell line, JIH-4, carrying a t(16;21)(p11.2;q22) and expressing the FUS-ERG fusion
    Jiang, Hui
    Qiu, Huiying
    Xue, Yongquan
    Pan, Jinlan
    Wu, Yafang
    Zhang, Jun
    Zheng, Jifu
    Wang, Qian
    Liang, Jianying
    Chen, Suning
    CANCER GENETICS, 2011, 204 (04) : 219 - 223
  • [29] The human LASP1 gene is fused to MLL in an acute myeloid leukemia with t(11;17)(q23;q21)
    Sabine Strehl
    Arndt Borkhardt
    Robert Slany
    Uta E Fuchs
    Margit König
    Oskar A Haas
    Oncogene, 2003, 22 : 157 - 160
  • [30] MULTIDRUG RESISTANCE-1 (MDR1) EXPRESSION AND FUNCTIONAL DYE DRUG EFFLUX IS HIGHLY CORRELATED WITH THE T(8,21) CHROMOSOMAL TRANSLOCATION IN PEDIATRIC ACUTE MYELOID-LEUKEMIA (AML)
    PEARSON, L
    LEITH, CP
    CHEN, IM
    DUNCAN, MH
    MCCONNELL, T
    THEIL, K
    FOURCAR, K
    WILLMAN, CL
    BLOOD, 1994, 84 (10) : A46 - A46