Blockage of RNA polymerase II at a cyclobutane pyrimidine dimer and 6-4 photoproduct

被引:53
作者
Kwei, JSM
Kuraoka, I
Horibata, K
Ubukata, M
Kobatake, E
Iwai, S
Handa, H
Tanaka, K
机构
[1] Osaka Univ, Grad Sch Frontier Biosci, Suita, Osaka 5650871, Japan
[2] Japan Sci & Technol Corp, CREST, Suita, Osaka 5650871, Japan
[3] Osaka Univ, Grad Sch Engn Sci, Toyonaka, Osaka 5608531, Japan
[4] Tokyo Inst Technol, Fac Biosci & Biotechnol, Yokohama, Kanagawa 2268501, Japan
[5] Tokyo Inst Technol, Frontier Collaborat Res Ctr, Yokohama, Kanagawa 2268501, Japan
关键词
RNA polymerase II; cyclobutane pyrimidine dimer; 6-4; photoproduct; transcription-coupled DNA repair; transcription elongation;
D O I
10.1016/j.bbrc.2004.06.066
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The blockage of transcription elongation by RNA polymerase II (pol II) at a DNA damage site on the transcribed strand triggers a transcription-coupled DNA repair (TCR), which rapidly removes DNA damage on the transcribed strand of the expressed gene and allows the resumption of transcription. To analyze the effect of UV-induced DNA damage on transcription elongation, an in vitro transcription elongation system using pol II and oligo (dC)-tailed templates containing a cyclobutane pyrimidine dimer (CPD) or 6-4 photoproduct (6-4PP) at a specific site was employed. The results showed that pol II incorporated nucleotides opposite the CPD and 6-4PP and then stalled. Pol II formed a stable ternary complex consisting of pol II, the DNA damage template, and the nascent transcript. Further-more, atomic force microscopy imaging revealed that pol II stalled at the damaged region. These findings may provide the basis for analysis of the initiation step of TCR. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1133 / 1138
页数:6
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