Repository logo
Log in(current)
Repository logoMIT Open ScholarshipDSpace@MIT
  1. Home
  2. MIT Open Access Articles
  3. MIT Open Access Articles
  4. Topological organization of multi-chromosomal regions by Firre

Topological organization of multi-chromosomal regions by Firre

Thumbnail Image
Download
Name

Lander_Topological organization.pdf

Size

4.04 MB

Format

Adobe PDF

Checksum (MD5)

768748bbcd3b3241f96a9380213518a4

Author(s)
Hacisuleyman, Ezgi
•
Trapnell, Cole
•
Williams, Adam
•
Henao-Mejia, Jorge
•
Sun, Lei
•
McClanahan, Patrick
•
Hendrickson, David G.
•
Sauvageau, Martin
•
Kelley, David R.
•
Morse, Michael
more
Alternative Title
Topological organization of multichromosomal regions by the long intergenic noncoding RNA Firre
Date Issued
January 2014
Journal
Nature Structural & Molecular Biology
Publisher
Nature Publishing Group
Citation
Hacisuleyman, Ezgi, Loyal A Goff, Cole Trapnell, Adam Williams, Jorge Henao-Mejia, Lei Sun, Patrick McClanahan, et al. “Topological Organization of Multichromosomal Regions by the Long Intergenic Noncoding RNA Firre.” Nature Structural & Molecular Biology 21, no. 2 (January 26, 2014): 198–206.
Version
Author's final manuscript
Abstract
RNA, including long noncoding RNA (lncRNA), is known to be an abundant and important structural component of the nuclear matrix. However, the molecular identities, functional roles and localization dynamics of lncRNAs that influence nuclear architecture remain poorly understood. Here, we describe one lncRNA, ​Firre, that interacts with the nuclear-matrix factor ​hnRNPU through a 156-bp repeating sequence and localizes across an ~5-Mb domain on the X chromosome. We further observed ​Firre localization across five distinct trans-chromosomal loci, which reside in spatial proximity to the ​Firre genomic locus on the X chromosome. Both genetic deletion of the ​Firre locus and knockdown of ​hnRNPU resulted in loss of colocalization of these trans-chromosomal interacting loci. Thus, our data suggest a model in which lncRNAs such as ​Firre can interface with and modulate nuclear architecture across chromosomes.
MIT Department
Massachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory
Massachusetts Institute of Technology. Department of Biological Engineering
Massachusetts Institute of Technology. Department of Biology
Terms of Use
Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
Persistent DSpace Link
http://hdl.handle.net/1721.1/96679
DOI of Published Version
https://doi.org/10.1038/nsmb.2764
Repository logo
PrivacyPermissionsAccessibilityContact us
Repository logo
Notify us about copyright concerns.