Tornaletti Silvia, Patrick Steve M, Turchi John J, Hanawalt Philip C
Department of Biological Sciences, Stanford University, Stanford, California 94305-5020, USA.
J Biol Chem. 2003 Sep 12;278(37):35791-7. doi: 10.1074/jbc.M305394200. Epub 2003 Jun 26.
Transcription-coupled DNA repair is dedicated to the removal of DNA lesions from transcribed strands of expressed genes. RNA polymerase arrest at a lesion has been proposed as a sensitive signal for recruitment of repair enzymes to the lesion site. To understand how initiation of transcription-coupled repair may occur, we have characterized the properties of the transcription complex when it encounters a lesion in its path. Here we have compared the effect of cisplatin-induced intrastrand cross-links on transcription elongation by T7 RNA polymerase and mammalian RNA polymerase II. We found that a single cisplatin 1,2-d(GG) intrastrand cross-link or a single cisplatin 1,3-d(GTG) intrastrand cross-link is a strong block to both polymerases. Furthermore, the efficiency of the block at a cisplatin 1,2-d(GG) intrastrand cross-link was similar in several different nucleotide sequence contexts. Interestingly, some blockage was also observed when the single cisplatin 1,3-d(GTG) intrastrand cross-link was located in the non-transcribed strand. Transcription complexes arrested at the cisplatin adducts were substrates for the transcript cleavage reaction mediated by the elongation factor TFIIS, indicating that the RNA polymerase II complexes arrested at these lesions are not released from template DNA. Addition of TFIIS yielded a population of transcripts up to 30 nucleotides shorter than those arrested at the lesion. In the presence of nucleoside triphosphates, these shortened transcripts could be re-elongated up to the site of the lesion, indicating that the arrested complexes are stable and competent to resume elongation. These results show that cisplatin-induced lesions in the transcribed DNA strand constitute a strong physical barrier to RNA polymerase progression, and they support current models of transcription arrest and initiation of transcription-coupled repair.
转录偶联DNA修复专门用于从表达基因的转录链中去除DNA损伤。RNA聚合酶在损伤处停滞被认为是将修复酶招募到损伤位点的敏感信号。为了了解转录偶联修复的起始过程是如何发生的,我们已经表征了转录复合物在其路径中遇到损伤时的特性。在这里,我们比较了顺铂诱导的链内交联对T7 RNA聚合酶和哺乳动物RNA聚合酶II转录延伸的影响。我们发现,单个顺铂1,2-d(GG)链内交联或单个顺铂1,3-d(GTG)链内交联对两种聚合酶都是很强的阻碍。此外,在几种不同的核苷酸序列背景下,顺铂1,2-d(GG)链内交联处的阻碍效率相似。有趣的是,当单个顺铂1,3-d(GTG)链内交联位于非转录链时,也观察到了一些阻碍。停滞在顺铂加合物处的转录复合物是延伸因子TFIIS介导的转录物切割反应的底物,这表明停滞在这些损伤处的RNA聚合酶II复合物没有从模板DNA上释放。添加TFIIS产生了一群比停滞在损伤处的转录物短30个核苷酸的转录物。在存在核苷三磷酸的情况下,这些缩短的转录物可以重新延伸到损伤位点,这表明停滞的复合物是稳定的,并且有能力恢复延伸。这些结果表明,转录DNA链中顺铂诱导的损伤对RNA聚合酶的前进构成了强大的物理障碍,并且它们支持当前的转录停滞和转录偶联修复起始模型。