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    <link>https://scholar.dgist.ac.kr/handle/20.500.11750/13653</link>
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    <pubDate>Sat, 04 Apr 2026 13:35:10 GMT</pubDate>
    <dc:date>2026-04-04T13:35:10Z</dc:date>
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      <title>How does cohesin organize the 3D genome?</title>
      <link>https://scholar.dgist.ac.kr/handle/20.500.11750/17231</link>
      <description>Title: How does cohesin organize the 3D genome?
Author(s): Finkelstein, Ilya; Zhang, Hongshan; Shi, Zhubing; Kim, Yoori; Yu, Hongtao; Bai, Xiao-Chen
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.</description>
      <pubDate>Sat, 02 Apr 2022 15:00:00 GMT</pubDate>
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      <dc:date>2022-04-02T15:00:00Z</dc:date>
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