Transcription of the XRCC1 gene in kidneys of radiosensitive and radioresistant mice following whole-body irradiation

被引:2
作者
Labudova, O
Hardmeier, R
Kitzmüller, E
Rink, H
Lubec, G
机构
[1] Univ Vienna, Dept Pediat, A-1090 Vienna, Austria
[2] Univ Bonn, Dept Radiobiol, D-5300 Bonn, Germany
来源
NEPHRON | 1998年 / 79卷 / 01期
关键词
XRCC1; gene; transcription; radiation resistance;
D O I
10.1159/000044993
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The XRCC1 gene was described to play a role in the sensitivity of mammalian cell lines towards ionizing irradiation. Cells with a mutation of this gene present with decreased single-strand break repair and reduced recombination repair, show increased double-strand breaks, and the sister chromatid exchange is increased up to tenfold. The goal of our study was to investigate the transcription of this gene in the kidney following ionizing irradiation in the mouse, as this could be relevant to the pathogenetic mechanisms found in radiation nephropathy. Furthermore, we intended to examine whether radiation-sensitive mice would show a transcriptional pattern different from radiation-resistant mice. Radiation-sensitive BALB/c/J/Him mice and radiation-resistant C3H/He/Him mice were whole body irradiated with X-ray at 2, 4, and 6 Gy and sacrificed 5, 15, and 30 min after irradiation. mRNA was isolated from kidney cortex and hybridized with probes for XRCC1 and p-actin as a housekeeping gene control. Following irradiation at 2 Gy, radiation-resistant mice increased transcriptional levels of mRNA-XRCC1/mRNA-beta-actin as early as after 5 min, and 15 and 30 min after irradiation, XRCC1 transcription was still higher than in radiation-sensitive mice. At higher radiation doses, no differences were found. This finding is the first in vivo study on XRCC1 of this kind and may in part explain the differences in the radiation sensitivity between the two strains studied.
引用
收藏
页码:61 / 66
页数:6
相关论文
共 29 条
[21]   DETECTION OF SPECIFIC SEQUENCES AMONG DNA FRAGMENTS SEPARATED BY GEL-ELECTROPHORESIS [J].
SOUTHERN, EM .
JOURNAL OF MOLECULAR BIOLOGY, 1975, 98 (03) :503-+
[22]   A CHO-CELL STRAIN HAVING HYPERSENSITIVITY TO MUTAGENS, A DEFECT IN DNA STRAND-BREAK REPAIR, AND AN EXTRAORDINARY BASELINE FREQUENCY OF SISTER-CHROMATID EXCHANGE [J].
THOMPSON, LH ;
BROOKMAN, KW ;
DILLEHAY, LE ;
CARRANO, AV ;
MAZRIMAS, JA ;
MOONEY, CL ;
MINKLER, JL .
MUTATION RESEARCH, 1982, 95 (2-3) :427-440
[23]   MOLECULAR-CLONING OF THE HUMAN XRCC1 GENE, WHICH CORRECTS DEFECTIVE-DNA STRAND BREAK REPAIR AND SISTER CHROMATID EXCHANGE [J].
THOMPSON, LH ;
BROOKMAN, KW ;
JONES, NJ ;
ALLEN, SA ;
CARRANO, AV .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (12) :6160-6171
[24]  
VANANKEREN SC, 1988, RADIAT RES, V116, P223
[25]  
WEI QY, 1995, CANCER RES, V55, P5025
[26]  
WEI YF, 1995, MOL CELL BIOL, V15, P3206
[27]  
WHITE BA, 1982, J BIOL CHEM, V257, P8569
[28]   ALTERATIONS IN EXPRESSION AND STRUCTURE OF THE DNA-REPAIR GENE XRCC1 [J].
YOO, HY ;
LI, L ;
SACKS, PG ;
THOMPSON, LH ;
BECKER, FF ;
CHAN, JYH .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 186 (02) :900-910
[29]   EXPRESSION OF THE DNA-REPAIR GENE XRCC1 IN BABOON TISSUES [J].
ZHOU, ZQ ;
WALTER, CA .
MUTATION RESEARCH LETTERS, 1995, 348 (03) :111-116