Abstract
Damage-induced long non-coding RNAs (dilncRNA) synthesized at DNA double-strand breaks (DSBs) by RNA polymerase II are necessary for DNA-damage-response (DDR) focus formation. We demonstrate that induction of DSBs results in the assembly of functional promoters that include a complete RNA polymerase II preinitiation complex, MED1 and CDK9. Absence or inactivation of these factors causes a reduction in DDR foci both in vivo and in an in vitro system that reconstitutes DDR events on nucleosomes. We also show that dilncRNAs drive molecular crowding of DDR proteins, such as 53BP1, into foci that exhibit liquid-liquid phase-separation condensate properties. We propose that the assembly of DSB-induced transcriptional promoters drives RNA synthesis, which stimulates phase separation of DDR factors in the shape of foci.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Ataxia Telangiectasia Mutated Proteins / genetics
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Ataxia Telangiectasia Mutated Proteins / metabolism
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Cell Line, Tumor
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Cyclin-Dependent Kinase 9 / genetics*
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Cyclin-Dependent Kinase 9 / metabolism
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DNA / genetics*
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DNA / metabolism
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DNA Breaks, Double-Stranded
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DNA Repair*
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Gene Expression Regulation
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HEK293 Cells
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HeLa Cells
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Histones / genetics
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Histones / metabolism
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Humans
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Mediator Complex Subunit 1 / genetics
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Mediator Complex Subunit 1 / metabolism*
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Osteoblasts / cytology
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Osteoblasts / metabolism
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Promoter Regions, Genetic
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RNA Polymerase II / genetics
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RNA Polymerase II / metabolism
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RNA, Long Noncoding / genetics
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RNA, Long Noncoding / metabolism
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Signal Transduction
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Transcription, Genetic*
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Tumor Suppressor p53-Binding Protein 1 / genetics
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Tumor Suppressor p53-Binding Protein 1 / metabolism
Substances
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H2AX protein, human
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Histones
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MED1 protein, human
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Mediator Complex Subunit 1
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RNA, Long Noncoding
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TP53BP1 protein, human
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Tumor Suppressor p53-Binding Protein 1
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DNA
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ATM protein, human
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Ataxia Telangiectasia Mutated Proteins
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CDK9 protein, human
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Cyclin-Dependent Kinase 9
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RNA Polymerase II