ANALYSIS OF RESTRICTION ENZYME-INDUCED CHROMOSOME-ABERRATIONS IN THE INTERSTITIAL TELOMERIC REPEAT SEQUENCES OF CHO AND CHE CELLS BY FISH

被引:65
作者
BALAJEE, AS
OH, HJ
NATARAJAN, AT
机构
[1] LEIDEN STATE UNIV,DEPT RADIAT GENET & CHEM MUTAGENESIS,MGC,SYLVIUS LABS,2333 AL LEIDEN,NETHERLANDS
[2] INTERUNIV INST RADIOPATHOL & RADIAT PROTECT,JA COHEN INST,LEIDEN,NETHERLANDS
来源
MUTATION RESEARCH | 1994年 / 307卷 / 01期
关键词
INTERSTITIAL TELOMERIC REPEATS; FRAGILE SITES; CHROMOSOME BREAKAGE; FISH;
D O I
10.1016/0027-5107(94)90304-2
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The interstitial telomeric sequences have been suggested to be more susceptible to chromosome breakage and rejoining. In the present study, we tested this possibility by analysing the behaviour of intra-chromosomal telomeric sequences in restriction enzyme-treated CHO and CHE cells. These cell lines show large blocks of internal telomeric repeats adjacent to the centromeric regions of the chromosomes. In CHO cells, (TTAGGG)n repeats are localised only near the centromeric regions of many of the chromosomes while in CHE cells the telomeric repeat sequences are found at both the terminal and centromeric regions of the chromosomes. In CHO cells, 26% of the total aberrations induced by AluI and 22% of those induced by Hinfl were found to be involved with internal telomeric repeat sequences. In CHE cells, which possess telomeric repeats at both the terminal and interstitial regions, 39% of the aberrations induced by AluI and PuuII showed telomeric repeat signals. The proportion of acentric fragments with a telomeric repeat signal was higher in CHE than in CHO cells. Some of the damaged cells displayed an intense signal indicating the possible amplification of these repeats by telomerase. These results are in accordance with the suggestion that non-telomeric locations of telomeric repeat sequences are more prone to chromosome breakage and misrepair.
引用
收藏
页码:307 / 313
页数:7
相关论文
共 16 条
[1]   RESTRICTION ENDONUCLEASES DO INDUCE SISTER-CHROMATID EXCHANGES IN CHINESE-HAMSTER OVARY CELLS [J].
BALAJEE, AS ;
NATARAJAN, AT .
MUTATION RESEARCH, 1993, 302 (01) :25-31
[2]   MURINE RADIATION MYELOID LEUKEMOGENESIS - RELATIONSHIP BETWEEN INTERSTITIAL TELOMERE-LIKE SEQUENCES AND CHROMOSOME-2 FRAGILE SITES [J].
BOUFFLER, S ;
SILVER, A ;
PAPWORTH, D ;
COATES, J ;
COX, R .
GENES CHROMOSOMES & CANCER, 1993, 6 (02) :98-106
[3]   INDUCTION OF CHROMOSOMAL DAMAGE BY RESTRICTION ENDONUCLEASE IN CHO CELLS PORATED WITH STREPTOLYSIN-O [J].
BRYANT, PE .
MUTATION RESEARCH, 1992, 268 (01) :27-34
[4]   HUMAN TELOMERIC 6-19 TRANSLOCATION CHROMOSOME WITH A TENDENCY TO BREAK AT THE FUSION POINT [J].
DRETS, ME ;
THERMAN, E .
CHROMOSOMA, 1983, 88 (02) :139-144
[5]   FUNCTIONAL REINTRODUCTION OF HUMAN TELOMERES INTO MAMMALIAN-CELLS [J].
FARR, C ;
FANTES, J ;
GOODFELLOW, P ;
COOKE, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (16) :7006-7010
[6]   HUMAN TELOMERES - FUSION AND INTERSTITIAL SITES [J].
HASTIE, ND ;
ALLSHIRE, RC .
TRENDS IN GENETICS, 1989, 5 (10) :326-331
[7]   IMPROVED TELOMERE DETECTION USING A TELOMERE REPEAT PROBE (TTAGGG)N GENERATED BY PCR [J].
IJDO, JW ;
WELLS, RA ;
BALDINI, A ;
REEDERS, ST .
NUCLEIC ACIDS RESEARCH, 1991, 19 (17) :4780-4780
[8]   ORIGIN OF HUMAN CHROMOSOME-2 - AN ANCESTRAL TELOMERE TELOMERE FUSION [J].
IJDO, JW ;
BALDINI, A ;
WARD, DC ;
REEDERS, ST ;
WELLS, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (20) :9051-9055
[9]   INTERSTITIAL TELOMERES ARE HOTSPOTS FOR ILLEGITIMATE RECOMBINATION WITH DNA-MOLECULES INJECTED INTO THE MACRONUCLEUS OF PARAMECIUM-PRIMAURELIA [J].
KATINKA, MD ;
BOURGAIN, FM .
EMBO JOURNAL, 1992, 11 (02) :725-732
[10]   CONSERVATION OF THE HUMAN TELOMERE SEQUENCE (TTAGGG)N AMONG VERTEBRATES [J].
MEYNE, J ;
RATLIFF, RL ;
MOYZIS, RK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (18) :7049-7053