Subcellular localization of a and B Nm23/NDPK subunits

被引:47
作者
Bosnar, MH
de Gunzburg, J
Bago, R
Brecevic, L
Weber, I
Pavelic, J
机构
[1] Rudjer Boskovic Inst, Div Mol Med, Mol Oncol Lab, Zagreb 10002, Croatia
[2] Inst Curie, INSERM, U528, Lab Signal Transduct & Oncogenesis, F-75248 Paris 05, France
[3] Univ Zagreb, Sch Med, Croatian Brain Res Inst, Dept Cytogenet, Zagreb 10002, Croatia
[4] Rudjer Boskovic Inst, Div Mol Biol, Lab Electron Microscopy, Zagreb 10002, Croatia
关键词
nm23; head and neck tumor cell lines; endoplasmic reticulum; green fluorescent protein;
D O I
10.1016/j.yexcr.2004.04.018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The human Nm23-H1/NDPK A and Nm23-H2/NDPK B encode for two subunits of nucleoside diphosphate kinase-a ubiquitous enzyme that transfers the terminal phosphates from ATP to (d)NDPs. Although having an 88% amino acid sequence identity and an already assigned biochemical role in the cell, the two subunits appear to have additional and distinctive cell functions. In particular, both subunits have been reported to be involved in tumor progression and metastasis. The aim of this study was to determine the specific, and potentially distinct, localizations of both subunits in tumor cells of different origin and differentiation and therefore to search for a possible link between their localization and the stage of disease. We used the GFP reporter system to analyze the ectopic expression of GFP-Nm23 proteins in head and neck tumor cell lines by fluorescent microscopy techniques. Our experiments revealed that GFP-fused Nm23-H1 and -H2 proteins display the same localization in transfected cells, regardless of their origin and differentiation status. The proteins are principally found in the cytosol and the endoplasmic reticulum. Moreover, some cells exhibit nuclear staining, which appears to be cell cycle-dependent. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:275 / 284
页数:10
相关论文
共 36 条
  • [1] BEVILACQUA G, 1990, PATHOL BIOL, V38, P774
  • [2] A DROSOPHILA GENE THAT IS HOMOLOGOUS TO A MAMMALIAN GENE ASSOCIATED WITH TUMOR-METASTASIS CODES FOR A NUCLEOSIDE DIPHOSPHATE KINASE
    BIGGS, J
    HERSPERGER, E
    STEEG, PS
    LIOTTA, LA
    SHEARN, A
    [J]. CELL, 1990, 63 (05) : 933 - 940
  • [3] Loss of heterozygosity of the nm23-H1 gene in human renal cell carcinomas
    Bosnar, MH
    Pavelic, K
    Hrascan, R
    Zeljko, Z
    Krhen, I
    Marekovic, Z
    Krizanac, S
    Pavelic, J
    [J]. JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1997, 123 (09) : 485 - 488
  • [4] NM23 GENE-EXPRESSION CORRELATES WITH CELL-GROWTH RATE AND S-PHASE
    CALIGO, MA
    CIPOLLINI, G
    FIORE, L
    CALVO, S
    BASOLO, F
    COLLECCHI, P
    CIARDIELLO, F
    PEPE, S
    PETRINI, M
    BEVILACQUA, G
    [J]. INTERNATIONAL JOURNAL OF CANCER, 1995, 60 (06) : 837 - 842
  • [5] Cipollini G, 1997, INT J CANCER, V73, P297, DOI 10.1002/(SICI)1097-0215(19971009)73:2<297::AID-IJC22>3.0.CO
  • [6] 2-B
  • [7] Tumor suppressor NM23-H1 is a granzyme A-activated DNase during CTL-mediated apoptosis, and the nucleosome assembly protein SET is its inhibitor
    Fan, ZS
    Beresford, PJ
    Oh, DY
    Zhang, D
    Lieberman, J
    [J]. CELL, 2003, 112 (05) : 659 - 672
  • [8] FLORENES VA, 1992, CANCER RES, V52, P6088
  • [9] Integrin cytoplasmic domain-associated protein 1α (ICAP-1α) interacts directly with the metastasis suppressor nm23-H2, and both proteins are targeted to newly formed cell adhesion sites upon integrin engagement
    Fournier, HN
    Dupé-Manet, S
    Bouvard, D
    Lacombe, ML
    Marie, C
    Block, MR
    Albiges-Rizo, C
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (23) : 20895 - 20902
  • [10] Receptor activation regulates cortical, but not vesicular localization of NDP kinase
    Gallagher, BC
    Parrott, KA
    Szabo, G
    Otero, AD
    [J]. JOURNAL OF CELL SCIENCE, 2003, 116 (15) : 3239 - 3250