Identification of novel Myc target genes with a potential role in lymphomagenesis

被引:36
作者
Marinkovic, D
Marinkovic, T
Kokai, E
Barth, T
Möller, P
Wirth, T
机构
[1] Univ Ulm, Dept Physiol Chem, D-89081 Ulm, Germany
[2] Univ Ulm, Inst Pathol, D-89081 Ulm, Germany
关键词
D O I
10.1093/nar/gkh877
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 c-Myc transcription factor regulates a wide set of genes involved in processes such as proliferation, differentiation and apoptosis. Therefore, altered expression of Myc leads to deregulation of a large number of target genes and, as a consequence, to tumorigenesis. For understanding Myc-induced transformation, identification of these target genes is essential. In this study, we searched for Myc target genes involved in lymphomagenesis using different mouse T and B cell lymphoma cell lines transformed by a conditional Myc-allele. Target genes obtained by microarray experiments were further subjected to a kinetic analysis of mRNA expression upon Myc inactivation/reactivation, bioinformatic examination of Myc binding sites and chromatin immunoprecipitation. This approach allowed us to define targets whose activation is a direct consequence of Myc binding. Among the 38 novel Myc targets, we identified several genes implicated in the tumor development. These genes are not only relevant for mouse lymphomas because we observed their upregulation in human lymphomas as well. Our findings further the understanding of Myc-induced lymphomagenesis and help toward developing more efficient antitumor strategies.
引用
收藏
页码:5368 / 5378
页数:11
相关论文
共 70 条
  • [1] Expression of multiple genes regulating cell cycle and apoptosis in differentiating hematopoietic cells is dependent on iron
    Alcantara, O
    Kalidas, M
    Baltathakis, I
    Boldt, DH
    [J]. EXPERIMENTAL HEMATOLOGY, 2001, 29 (09) : 1060 - 1069
  • [2] THE C-MYC PROTEIN INDUCES CELL-CYCLE PROGRESSION AND APOPTOSIS THROUGH DIMERIZATION WITH MAX
    AMATI, B
    LITTLEWOOD, TD
    EVAN, GI
    LAND, H
    [J]. EMBO JOURNAL, 1993, 12 (13) : 5083 - 5087
  • [3] ONCOGENIC ACTIVITY OF THE C-MYC PROTEIN REQUIRES DIMERIZATION WITH MAX
    AMATI, B
    BROOKS, MW
    LEVY, N
    LITTLEWOOD, TD
    EVAN, GI
    LAND, H
    [J]. CELL, 1993, 72 (02) : 233 - 245
  • [4] Growth retardation, polyploidy, and multinucleation induced by Clast3, a novel cell cycle-regulated protein
    Bahar, R
    O-Wang, JY
    Kawamura, K
    Seimiya, M
    Wang, YQ
    Hatano, M
    Okada, S
    Tokuhisa, T
    Watanabe, T
    Tagawa, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (42) : 40012 - 40019
  • [5] Homogeneous immunophenotype and paucity of secondary genomic aberrations are distinctive features of endemic but not of sporadic Burkitt's lymphoma and diffuse large B-cell lymphoma with MYC rearrangement
    Barth, TF
    Müller, S
    Pawlita, M
    Sebert, R
    Rother, JU
    Mechtersheimer, G
    Kitinya, J
    Bentz, M
    Möller, P
    [J]. JOURNAL OF PATHOLOGY, 2004, 203 (04) : 940 - 945
  • [6] THE ORNITHINE DECARBOXYLASE GENE IS A TRANSCRIPTIONAL TARGET OF C-MYC
    BELLOFERNANDEZ, C
    PACKHAM, G
    CLEVELAND, JL
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (16) : 7804 - 7808
  • [7] Bertoni F, 1999, GENE CHROMOSOME CANC, V26, P176, DOI 10.1002/(SICI)1098-2264(199910)26:2<176::AID-GCC11>3.0.CO
  • [8] 2-3
  • [9] BINDING OF MYC PROTEINS TO CANONICAL AND NONCANONICAL DNA-SEQUENCES
    BLACKWELL, TK
    HUANG, J
    MA, A
    KRETZNER, L
    ALT, FW
    EISENMAN, RN
    WEINTRAUB, H
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (09) : 5216 - 5224
  • [10] SEQUENCE-SPECIFIC DNA-BINDING BY THE C-MYC PROTEIN
    BLACKWELL, TK
    KRETZNER, L
    BLACKWOOD, EM
    EISENMAN, RN
    WEINTRAUB, H
    [J]. SCIENCE, 1990, 250 (4984) : 1149 - 1151