Detection of incomplete chromosome elements and interstitial fragments induced by bleomycin in hamster cells using a telomeric PNA probe

被引:23
作者
Bolzán, AD [1 ]
Bianchi, MS [1 ]
机构
[1] IMBICE, Lab Citogenet & Mutagenesis, RA-1900 La Plata, Argentina
关键词
telomeric probe; bleomycin; chromosome aberrations; incomplete chromosome elements; interstitial fragments;
D O I
10.1016/j.mrfmmm.2004.02.016
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The detection of incomplete chromosome elements (ICE, i.e., elements with telomeric signal at only one terminal end) and interstitial fragments induced by the radiomimetic compound bleomycin (BLM) was carried out in a Chinese hamster embryo (CHE)cell line using FISH with a telomeric peptide nucleic acid (PNA) probe. CHE cells were treated with 0, 1, 2.5, 5, and 7.5 mug/ml of BLM and chromosomal aberrations were analyzed in the first mitosis after treatment using a telomeric PNA probe. The relationship between chromosomal aberrations frequency and bleomycin concentration was of linear type (P < 0.05 for all type of aberrations analyzed, i.e., multicentric chromosomes, centric rings, interstitial fragments and ICE). After BLM treatment, about 20-30% of the analyzed metaphases contained one or more pairs of ICE. Acentric interstitial fragments, lacking telomeric signals, were observed with a frequency of about 4-7 times higher than the dicentric frequency. Acentric interstitial fragments and ICE were induced at similar frequencies, except for the lowest BLM concentration (1 mug/ml), where the latter ones showed a higher frequency than the former ones. Furthermore, it was estimated that about 53 % of excess acentric fragments originate from complete exchanges (interstitial deletions) and 47% from incomplete exchanges or terminal deletions. These results show that interstitial fragments and ICE are the most frequent asymmetrical chromosomal aberrations induced by BLM and indicate that true incompleteness is a common event following exposure to BLM. Moreover, the comparable trend of the concentration-response relationship for the different aberrations strongly suggests that all BLM-induced asymmetrical aberrations are formed by a similar underlying mechanism. (C) 2004 Elsevier B.V. All rights reserved.
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页码:1 / 8
页数:8
相关论文
共 27 条
[1]   ANALYSIS OF RESTRICTION ENZYME-INDUCED CHROMOSOME-ABERRATIONS IN THE INTERSTITIAL TELOMERIC REPEAT SEQUENCES OF CHO AND CHE CELLS BY FISH [J].
BALAJEE, AS ;
OH, HJ ;
NATARAJAN, AT .
MUTATION RESEARCH, 1994, 307 (01) :307-313
[2]  
BIANCHI NO, 1990, CANCER RES, V50, P2379
[3]  
Boei JJWA, 1998, INT J RADIAT BIOL, V73, P125, DOI 10.1080/095530098142491
[4]  
Boei JJWA, 2000, INT J RADIAT BIOL, V76, P163, DOI 10.1080/095530000138817
[5]   Detection of incomplete exchanges and interstitial fragments in X-irradiated human lymphocytes using a telomeric PNA probe [J].
Boei, JJWA ;
Vermeulen, S ;
Fomina, J ;
Natarajan, AT .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1998, 73 (06) :599-603
[6]   FISH analysis of telomeric repeat sequences and their involvement in chromosomal aberrations induced by radiomimetic compounds in hamster cells [J].
Bolzán, AD ;
Páez, GL ;
Bianchi, MS .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2001, 479 (1-2) :187-196
[7]   CYTOGENETIC EFFECT OF BLEOMYCIN ON HUMAN PERIPHERAL LYMPHOCYTES INVITRO AND INVIVO [J].
DRESP, J ;
SCHMID, E ;
BAUCHINGER, M .
MUTATION RESEARCH, 1978, 56 (03) :341-353
[8]   USE OF MULTICOLOR CHROMOSOME PAINTING TO IDENTIFY CHROMOSOMAL REARRANGEMENTS IN HUMAN-LYMPHOCYTES EXPOSED TO BLEOMYCIN - A COMPARISON WITH CONVENTIONAL CYTOGENETIC ANALYSIS OF GIEMSA-STAINED CHROMOSOMES [J].
ELLARD, S ;
PARRY, EM ;
PARRY, JM .
ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 1995, 26 (01) :44-54
[9]  
Fomina J, 2000, INT J RADIAT BIOL, V76, P807, DOI 10.1080/09553000050028968
[10]   Accurate detection of true incomplete exchanges in human lymphocytes exposed to neutron radiation using chromosome painting in combination with a telomeric PNA probe [J].
Fomina, J ;
Darroudi, F ;
Natarajan, AT .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 2001, 77 (12) :1175-1183