Molecular Basis of Transcriptional Mutagenesis at 8-Oxoguanine

被引:56
作者
Damsma, Gerke E.
Cramer, Patrick [1 ]
机构
[1] Univ Munich, Dept Chem & Biochem, Gene Ctr, D-81377 Munich, Germany
关键词
RNA-POLYMERASE-II; FIDELITY DNA-POLYMERASE; STRUCTURAL BASIS; DAMAGED DNA; ELONGATION; BYPASS; LESION; TRANSLOCATION; REPLICATION; COMPLEXES;
D O I
10.1074/jbc.M109.022764
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
Structure-function analysis has revealed the mechanism of yeast RNA polymerase II transcription at 8-oxoguanine (8-oxoG), the major DNA lesion resulting from oxidative stress. When polymerase II encounters 8-oxoG in the DNA template strand, it can misincorporate adenine, which forms a Hoogsteen bp with 8-oxoG at the active center. This requires rotation of the 8-oxoG base from the standard anti- to an uncommon syn-conformation, which likely occurs during 8-oxoG loading into the active site. The misincorporated adenine escapes intrinsic proofreading, resulting in transcriptional mutagenesis that is observed directly by mass spectrometric RNA analysis.
引用
收藏
页码:31658 / 31663
页数:6
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