In vivo cloning and characterization of a new growth suppressor protein TOE1 as a direct target gene of EGR1

被引:31
作者
de Belle, I [1 ]
Wu, JX
Sperandio, S
Mercola, D
Adamson, ED
机构
[1] La Jolla Canc Res Ctr, Burnham Inst, La Jolla, CA 92037 USA
[2] Buck Inst Age Res, Novato, CA 94945 USA
[3] Sidney Kimmel Canc Ctr, San Diego, CA 92121 USA
[4] Univ Calif San Diego, Ctr Canc, La Jolla, CA 92093 USA
关键词
D O I
10.1074/jbc.M210502200
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
Egr1, an immediate early transcription factor, responds to diverse stimuli and affects gene transcription to accomplish its biological effects. One important effect of Egr1 expression is to decrease the growth and tumorigenic potential of several tumor cell types. To identify important Egr1 target genes, we have adapted a methodology involving formaldehyde-induced protein-DNA cross-linking, chromatin immunoprecipitation, and multiplex PCR. Using this approach, we report the cloning of a new Egr1 target gene that is able to account, at least in part, for the growth inhibitory activity of Egr1. We have named this new protein TOE1 for target of Egr1.
引用
收藏
页码:14306 / 14312
页数:7
相关论文
共 32 条
  • [1] ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
  • [2] Involvement of the interaction between p21 and proliferating cell nuclear antigen for the maintenance of G2/M arrest after DNA damage
    Ando, T
    Kawabe, T
    Ohara, H
    Ducommun, B
    Itoh, M
    Okamoto, T
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (46) : 42971 - 42977
  • [3] NUCLEOLAR LOCALIZATION OF MYC TRANSCRIPTS
    BOND, VC
    WOLD, B
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (06) : 3221 - 3230
  • [4] Boyd KE, 1999, MOL CELL BIOL, V19, P8393
  • [5] Cheung TH, 1999, CANCER-AM CANCER SOC, V86, P1294, DOI 10.1002/(SICI)1097-0142(19991001)86:7<1294::AID-CNCR26>3.0.CO
  • [6] 2-O
  • [7] de Belle I, 2000, BIOTECHNIQUES, V29, P162
  • [8] P53 and Egr-1 additively suppress transformed growth in HT1080 cells but Egr-1 counteracts p53-dependent apoptosis
    de Belle, I
    Huang, RP
    Fan, Y
    Liu, CT
    Mercola, D
    Adamson, ED
    [J]. ONCOGENE, 1999, 18 (24) : 3633 - 3642
  • [9] The genomic sequences bound to special AT-rich sequence-binding protein 1 (SATB1) in vivo in Jurkat T cells are tightly associated with the nuclear matrix at the bases of the chromatin loops
    de Belle, I
    Cai, ST
    Kohwi-Shigematsu, T
    [J]. JOURNAL OF CELL BIOLOGY, 1998, 141 (02) : 335 - 348
  • [10] Calcitonin receptor-mediated growth suppression of HEK-293 cells is accompanied by induction of p21WAF1/CIP1 and G2/M arrest
    Evdokiou, A
    Raggatt, LJ
    Atkins, GJ
    Findlay, DM
    [J]. MOLECULAR ENDOCRINOLOGY, 1999, 13 (10) : 1738 - 1750