Sensitive genetic biomarkers for determining apoptosis in the brown bullhead (Ameiurus nebulosus)

被引:25
作者
Busch, CR
Heath, DD
Hubberstey, A
机构
[1] Univ Windsor, Dept Biol Sci, Windsor, ON N9B 3P4, Canada
[2] Univ Windsor, Great Lakes Inst Environm Res, Windsor, ON, Canada
关键词
transcription; TUNEL; programmed cell death; ecotoxicology; biomarker;
D O I
10.1016/j.gene.2004.01.004
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Biomarkers are necessary for monitoring environmentally induced alterations at the molecular level in order to assess the impact of xenobiotic compounds on organism health. Apoptosis is a highly regulated cellular process that controls programmed cell death and is involved in tumor formation. Apoptosis thus may provide the basis for developing biomarkers for use in the field of ecotoxicology to monitor non-lethal levels of xenobiotic induced cellular stress and toxicity. This study shows that a brown bullhead (Ameiurus nebulosus) fibroblast cell line (BB-2) responds to known apoptotic inducers (staurosporine, cycloheximide, and tumor necrosis factor alpha (TNF-alpha)), as characterized by terminal deoxynucleotidyl transferase (TdT)-mediated dUTP digoxigenin nick end-labelling (TUNEL). Furthermore, we characterized the apoptotic process using a series of newly identified bullhead genetic markers. Exposure to protein kinase C inhibitors altered the transcription of TF-cell apoptosis-related protein (TFAR)- 15 and p23 with no effect on p53, inhibitor of apoptosis protein (IAP), or PNAS-2. Inhibition of protein synthesis caused a consistent reduction in the transcription of p53 and PNAS-2. This study demonstrates that our novel transcriptional markers are sensitive biomarkers for the study of the effects of xenobiotic chemicals on apoptosis in the brown bullhead. (C) 2004 Elsevier B.V All rights reserved.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 34 条
[1]   Roles for p53 in growth arrest and apoptosis: putting on the brakes after genotoxic stress [J].
Amundson, SA ;
Myers, TG ;
Fornace, AJ .
ONCOGENE, 1998, 17 (25) :3287-3299
[2]   GENETIC AND MOLECULAR ECOTOXICOLOGY - A RESEARCH FRAMEWORK [J].
ANDERSON, S ;
SADINSKI, W ;
SHUGART, L ;
BRUSSARD, P ;
DEPLEDGE, M ;
FORD, T ;
HOSE, J ;
STEGEMAN, J ;
SUK, W ;
WIRGIN, I ;
WOGAN, G .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1994, 102 :3-8
[3]   IDENTIFICATION OF POTENTIAL FISH CARCINOGENS IN SEDIMENT FROM HAMILTON HARBOR, ONTARIO, CANADA [J].
BALCH, GC ;
METCALFE, CD ;
HUESTIS, SY .
ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY, 1995, 14 (01) :79-91
[4]  
BARR PJ, 1994, BIO-TECHNOL, V12, P487, DOI 10.1038/nbt0594-487
[5]  
Baumann Paul C., 1992, Journal of Aquatic Ecosystem Health, V1, P135, DOI 10.1007/BF00044045
[6]   Effects of chemical contaminants an genetic diversity in natural populations: implications for biomonitoring and ecotoxicology [J].
Bickham, JW ;
Sandhu, S ;
Hebert, PDN ;
Chikhi, L ;
Athwal, R .
MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH, 2000, 463 (01) :33-51
[7]   Apoptosis, PCNA, and p53 in Fundulus grandis fish liver after in vivo exposure to N-methyl-N′-nitro-N-nitrcssoguanidine and 2-aminofluorene [J].
Blas-Machado, U ;
Taylor, HW ;
Means, JC .
TOXICOLOGIC PATHOLOGY, 2000, 28 (04) :601-609
[8]   The mRNA of the translationally controlled tumor protein P23/TCTP is a highly structured RNA, which activates the dsRNA-dependent protein kinase PKR [J].
Bommer, UA ;
Borovjagin, AV ;
Greagg, MA ;
Jeffrey, IW ;
Russell, P ;
Laing, KG ;
Lee, M ;
Clemens, MJ .
RNA, 2002, 8 (04) :478-496
[9]   CYCLIN PCNA IS THE AUXILIARY PROTEIN OF DNA POLYMERASE-DELTA [J].
BRAVO, R ;
FRANK, R ;
BLUNDELL, PA ;
MACDONALDBRAVO, H .
NATURE, 1987, 326 (6112) :515-517
[10]   APOPTOSIS - MOLECULAR CONTROL POINT IN TOXICITY [J].
CORCORAN, GB ;
FIX, L ;
JONES, DP ;
MOSLEN, MT ;
NICOTERA, P ;
OBERHAMMER, FA ;
BUTTYAN, R .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1994, 128 (02) :169-181