Transient RNA-DNA Hybrids Are Required for Efficient Double-Strand Break Repair

Cell

Volumn 167, Issue 4, 2016, Pages 1001-1013.e7

  Ohle, Corina ^a   Tesorero, Rafael ^a   Schermann, Géza ^a   Dobrev, Nikolay ^a   Sinning, Irmgard ^a   Fischer, Tamás ^a,b  

^a UNIVERSITY OF HEIDELBERG   (Germany)

^b Australian National University   (Australia)

Author keywords

DNA repair; DSB repair; genome stability; homologous recombination; R loops; RNA DNA hybrids; RNase H; RPA

Indexed keywords

RIBONUCLEASE H; DNA; RIBONUCLEASE HI; RIBONUCLEASE HII; RNA; RNA POLYMERASE II;

ARTICLE; BINDING SITE; DNA BINDING; DNA DEGRADATION; DNA RNA HYBRIDIZATION; DNA STRAND BREAKAGE; ENZYME ACTIVITY; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; SCHIZOSACCHAROMYCES POMBE; DNA DAMAGE; ENZYMOLOGY; GENE EXPRESSION; GENETICS; GENOMIC INSTABILITY; METABOLISM; RECOMBINATION REPAIR; SCHIZOSACCHAROMYCES;

DNA; DNA DAMAGE; GENE EXPRESSION; GENOMIC INSTABILITY; RECOMBINATIONAL DNA REPAIR; RIBONUCLEASE H; RNA; RNA POLYMERASE II; SCHIZOSACCHAROMYCES;

EID: 84995654423     PISSN: 00928674     EISSN: 10974172     Source Type: Journal    
DOI: 10.1016/j.cell.2016.10.001     Document Type: Article

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