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5W51

Pol II elongation complex with an N6-methyladenine-containing template and a matched UMPNPP

Summary for 5W51
Entry DOI10.2210/pdb5w51/pdb
Related5w4u
DescriptorDNA-directed RNA polymerase II subunit RPB1, DNA-directed RNA polymerases I, II, and III subunit RPABC4, 29mer template DNA, ... (16 entities in total)
Functional Keywordscomplex, dna binding protein, dna binding protein-rna-dna complex, dna binding protein/rna/dna
Biological sourceSaccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast)
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Total number of polymer chains13
Total formula weight486808.44
Authors
Wang, W.,Wang, D. (deposition date: 2017-06-13, release date: 2018-06-20, Last modification date: 2023-10-04)
Primary citationWang, W.,Xu, L.,Hu, L.,Chong, J.,He, C.,Wang, D.
Epigenetic DNA Modification N6-Methyladenine Causes Site-Specific RNA Polymerase II Transcriptional Pausing.
J.Am.Chem.Soc., 139:14436-14442, 2017
Cited by
PubMed Abstract: N-Methyladenine (N-mA or 6 mA) is an epigenetic DNA modification in eukaryotic genomes. In contrast to the well-established roles of 5-methylcytosine for epigenetic regulation of gene expression, the functional roles of N-mA remain elusive. In particular, the impact of N-mA modification of the DNA template on RNA polymerase II (pol II) transcription elongation is not known. In this work, using the Saccharomyces cerevisiae pol II transcriptional elongation system as a model, we investigated the molecular mechanism of pol II recognition and processing of N-mA sites via both biochemical and structural approaches. We found that N-mA causes site-specific pol II pausing/stalling. Structural analysis revealed that while N-mA can reach the +1 template position, the stability of the N-mA and UTP base pairing is compromised. Taken together, we reveal that the presence of the 6-methyl group on adenine reduces incorporation efficiency and promotes backtracking translocation. Our studies with yeast pol II provide molecular insights into understanding the impacts of N-mA on pol II transcription dynamics in different organisms.
PubMed: 28933854
DOI: 10.1021/jacs.7b06381
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.404 Å)
Structure validation

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