The Xist lncRNA Exploits Three-Dimensional Genome Architecture to Spread Across the X Chromosome

Author:

Engreitz Jesse M.12,Pandya-Jones Amy3,McDonel Patrick1,Shishkin Alexander1,Sirokman Klara1,Surka Christine1,Kadri Sabah1,Xing Jeffrey1,Goren Alon1,Lander Eric S.145,Plath Kathrin3,Guttman Mitchell1

Affiliation:

1. Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA.

2. Division of Health Sciences and Technology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

3. Department of Biological Chemistry, Jonsson Comprehensive Cancer Center, Molecular Biology Institute, and Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, David Geffen School of Medicine, University of California, Los Angeles, CA 90095, USA.

4. Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

5. Department of Systems Biology, Harvard Medical School, Boston, MA 02114, USA.

Abstract

Understanding Xist-ance Large noncoding RNAs (lncRNAs) are increasingly appreciated to play important roles in the cell. A number of lncRNAs act to target chromatin regulatory complexes to their sites of action. Engreitz et al. (p. 10.1126/science.1237973 , published online 4 July; see the Perspective by Dimond and Fraser ) found that the mouse Xist lncRNA, which initiates X-chromosome inactivation, was transferred from its site of transcription to distant sites on the X chromosome purely through their close three-dimensional proximity to the Xist gene. Xist initially localized to the periphery of active genes on the X chromosome but gradually spread across them using its A-repeat domain, until the Xist RNA bound broadly across the inactive X chromosome in differentiated female cells.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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