Molecular Cell, volume 76, issue 3, pages 412-42200000
RNA Interactions Are Essential for CTCF-Mediated Genome Organization.
Ricardo Saldaña Meyer
1
,
Javier Rodriguez-Hernaez
2
,
Thelma Escobar
1
,
Mayilaadumveettil Nishana
2
,
Karina Jácome López
3
,
Elphège P. Nora
4, 5
,
Aristotelis Tsirigos
6, 7
,
Mayra Furlan-Magaril
3
,
Jane Skok
2
,
Danny Reinberg
1
2
Department of Pathology, NYULSoM, New York, NY, USA.
|
5
6
Department of Pathology, NYULSoM, New York, NY, USA
|
Publication type: Journal Article
Publication date: 2019-11-01
Journal:
Molecular Cell
scimago Q1
SJR: 9.332
CiteScore: 26.0
Impact factor: 14.5
ISSN: 10972765, 10974164
PubMed ID:
31522988
Molecular Biology
Cell Biology
Abstract
The function of the CCCTC-binding factor (CTCF) in the organization of the genome has become an important area of investigation, but the mechanisms by which CTCF dynamically contributes to genome organization are not clear. We previously discovered that CTCF binds to large numbers of endogenous RNAs, promoting its self-association. In this regard, we now report two independent features that disrupt CTCF association with chromatin: inhibition of transcription and disruption of CTCF-RNA interactions through mutations of 2 of its 11 zinc fingers that are not required for CTCF binding to its cognate DNA site: zinc finger 1 (ZF1) or zinc finger 10 (ZF10). These mutations alter gene expression profiles as CTCF mutants lose their ability to form chromatin loops and thus the ability to insulate chromatin domains and to mediate CTCF long-range genomic interactions. Our results point to the importance of CTCF-mediated RNA interactions as a structural component of genome organization.
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