RNA polymerase II stalled at a thymine dimer: footprint and effect on excision repair. - Wikidata - awgldk - TriplyDB

RNA polymerase II stalled at a thymine dimer: footprint and effect on excision repair.

RNA polymerase II stalled at a thymine dimer: footprint and effect on excision repair.

http://www.wikidata.org/entity/Q39719255

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DNA repair: dynamic defenders against cancer and aging The ATPase domain but not the acidic region of Cockayne syndrome group B gene product is essential for DNA repair A human RNA polymerase II transcription termination factor is a SWI2/SNF2 family member Cockayne syndrome group B protein enhances elongation by RNA polymerase II Structure-function studies of the RNA polymerase II elongation complex A cryptochrome/photolyase class of enzymes with single-stranded DNA-specific photolyase activity Functional TFIIH is required for UV-induced translocation of CSA to the nuclear matrix Mammalian transcription-coupled excision repair Mechanism of Translesion Transcription by RNA Polymerase II and Its Role in Cellular Resistance to DNA Damage A new connection of mRNP biogenesis and export with transcription-coupled repair ELA1 and CUL3 are required along with ELC1 for RNA polymerase II polyubiquitylation and degradation in DNA-damaged yeast cells Human transcription release factor 2 dissociates RNA polymerases I and II stalled at a cyclobutane thymine dimer RNA polymerase II elongation complexes containing the Cockayne syndrome group B protein interact with a molecular complex containing the transcription factor IIH components xeroderma pigmentosum B and p62 An in vitro method for detecting genetic toxicity based on inhibition of RNA synthesis by DNA lesions Transcription-coupled DNA repair: two decades of progress and surprises Damaged DNA-binding protein DDB stimulates the excision of cyclobutane pyrimidine dimers in vitro in concert with XPA and replication protein A.Detection and determination of oligonucleotide triplex formation-mediated transcription-coupled DNA repair in HeLa nuclear extracts.Base pair opening in a deoxynucleotide duplex containing a cis-syn thymine cyclobutane dimer lesion.DNA damage in the nucleosome core is refractory to repair by human excision nuclease.Recognition and repair of the cyclobutane thymine dimer, a major cause of skin cancers, by the human excision nuclease.Convergent transcription through a long CAG tract destabilizes repeats and induces apoptosis Transcription-dependent cytosine deamination is a novel mechanism in ultraviolet light-induced mutagenesis.Accessing DNA damage in chromatin: insights from transcription.Nucleosome structure and positioning modulate nucleotide excision repair in the non-transcribed strand of an active gene Thymine dimer-induced structural changes to the DNA duplex examined with reactive probes (†).UVB induces a genome-wide acting negative regulatory mechanism that operates at the level of transcription initiation in human cells.Recombinational repair and restart of damaged replication forks.Roles for the transcription elongation factor NusA in both DNA repair and damage tolerance pathways in Escherichia coli Yeast RAD26, a homolog of the human CSB gene, functions independently of nucleotide excision repair and base excision repair in promoting transcription through damaged bases The stalling of transcription at abasic sites is highly mutagenic.Transcription bypass of DNA lesions enhances cell survival but attenuates transcription coupled DNA repair.Reduced RNA polymerase II transcription in extracts of cockayne syndrome and xeroderma pigmentosum/Cockayne syndrome cells.RNA polymerase II transcription inhibits DNA repair by photolyase in the transcribed strand of active yeast genes.H2A.Z nucleosomes enriched over active genes are homotypic.ATP-dependent chromatin remodeling by Cockayne syndrome protein B and NAP1-like histone chaperones is required for efficient transcription-coupled DNA repair Nucleotide excision repair and photolyase preferentially repair the nontranscribed strand of RNA polymerase III-transcribed genes in Saccharomyces cerevisiae Evaluation of sgRNA target sites for CRISPR-mediated repression of TP53 Genome-wide analysis of human global and transcription-coupled excision repair of UV damage at single-nucleotide resolution RNA polymerase: the most specific damage recognition protein in cellular responses to DNA damage?Structural characterization of RNA polymerase II complexes arrested by a cyclobutane pyrimidine dimer in the transcribed strand of template DNA.

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P2860

RNA polymerase II stalled at a thymine dimer: footprint and effect on excision repair.

http://www.wikidata.org/entity/Q39719255

description

1997 nî lūn-bûn

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1997年論文

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1997年論文

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1997年论文

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1997年论文

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1997年论文

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name

RNA polymerase II stalled at a thymine dimer: footprint and effect on excision repair.

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RNA polymerase II stalled at a thymine dimer: footprint and effect on excision repair.

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type

label

RNA polymerase II stalled at a thymine dimer: footprint and effect on excision repair.

@en

RNA polymerase II stalled at a thymine dimer: footprint and effect on excision repair.

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prefLabel

RNA polymerase II stalled at a thymine dimer: footprint and effect on excision repair.

@en

RNA polymerase II stalled at a thymine dimer: footprint and effect on excision repair.

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Nucleic Acids Research

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RNA polymerase II stalled at a thymine dimer: footprint and effect on excision repair.

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Reinberg D

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Sancar A

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Selby CP

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P2860

Human cyclin-dependent kinase-activating kinase exists in three distinct complexes

Human transcription-repair coupling factor CSB/ERCC6 is a DNA-stimulated ATPase but is not a helicase and does not disrupt the ternary transcription complex of stalled RNA polymerase II

Interactions involving the human RNA polymerase II transcription/nucleotide excision repair complex TFIIH, the nucleotide excision repair protein XPG, and Cockayne syndrome group B (CSB) protein

Association of human protein-tyrosine phosphatase kappa with members of the armadillo family

ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes

Transcript cleavage by RNA polymerase II arrested by a cyclobutane pyrimidine dimer in the DNA template

Recycling of the general transcription factors during RNA polymerase II transcription

Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene

The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA.

RNA polymerase II elongation complexes paused after the synthesis of 15- or 35-base transcripts have different structures

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10.1093/NAR/25.4.787

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