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              <classCode scheme="mesh">Transcription Factors, TFII</classCode>
              <classCode scheme="mesh">Transcription, Genetic</classCode>
              <classCode scheme="mesh">Transcriptional Elongation Factors</classCode>
              <classCode scheme="mesh">Uracil</classCode>
              <classCode scheme="mesh">DNA Repair</classCode>
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              <classCode scheme="mesh">Guanine</classCode>
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              <classCode scheme="mesh">Humans</classCode>
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              <p>Oxidative lesions represent the most abundant DNA lesions within the cell. In the present study, we investigated the impact of the oxidative lesions 8-oxoguanine, thymine glycol and 5-hydroxyuracil on RNA polymerase II (RNA pol II) transcription using a well-defined in vitro transcription system. We found that in a purified, reconstituted transcription system, these lesions block elongation by RNA pol II to different extents, depending on the type of lesion. Suggesting the presence of a bypass activity, the block to elongation is alleviated when transcription is carried out in HeLa cell nuclear extracts. By purifying this activity, we discovered that TFIIF could promote elongation through a thymine glycol lesion. The elongation factors Elongin and CSB, but not TFIIS, can also stimulate bypass of thymine glycol lesions, whereas Elongin, CSB and TFIIS can all enhance bypass of an 8-oxoguanine lesion. By increasing the efficiency with which RNA pol II reads through oxidative lesions, elongation factors can contribute to transcriptional mutagenesis, an activity that could have implications for the generation or progression of human diseases.</p>
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