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dc.contributor.author Finkelstein, Ilya -
dc.contributor.author Zhang, Hongshan -
dc.contributor.author Shi, Zhubing -
dc.contributor.author Kim, Yoori -
dc.contributor.author Yu, Hongtao -
dc.contributor.author Bai, Xiao-Chen -
dc.date.accessioned 2022-12-07T10:40:12Z -
dc.date.available 2022-12-07T10:40:12Z -
dc.date.created 2022-12-07 -
dc.date.issued 2022-04-03 -
dc.identifier.issn 0892-6638 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/17231 -
dc.description.abstract Cohesin and CCCTC-binding factor (CTCF) are key regulatory proteins of three-dimensional (3D) genome organization. I will present direct evidence that cohesin extrudes DNA loops that are anchored by CTCF proteins in specific orientations. CTCF binding polarity controls cohesin-mediated DNA looping. Using single-molecule imaging of CTCF-cohesin collisions, we demonstrate that the N-terminus of CTCF must be oriented towards cohesin to block its ability to compact DNA. C-terminally oriented CTCF accelerates DNA compaction by cohesin. Oriented inactive Cas9 and Cas12a ribonucleoproteins exhibit similar polar effects on DNA compaction by cohesin. RNA-DNA hybrids (R-loops), such as those that occur at highly transcribed genes, efficiently block cohesin-mediated DNA compaction. Our results explain long-standing puzzles regarding how CTCF and transcription shape the 3D genome. © FASEB. -
dc.language English -
dc.publisher Federation of American Societies for Experimental Biology -
dc.title How does cohesin organize the 3D genome? -
dc.type Conference Paper -
dc.identifier.doi 10.1096/fasebj.2022.36.S1.0I131 -
dc.identifier.bibliographicCitation Experimental Biology 2022 -
dc.identifier.url https://www.eventscribe.net/2022/EB2022/biography.asp?pfp=Speakers -
dc.citation.conferencePlace US -
dc.citation.conferencePlace Philadelphia -
dc.citation.title Experimental Biology 2022 -
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Department of New Biology Molecular Epigenetics Lab 2. Conference Papers

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