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      DNMT1-interacting RNAs block gene specific DNA methylation

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          Summary

          DNA methylation was described almost a century ago. However, the rules governing its establishment and maintenance remain elusive. Here, we present data demonstrating that active transcription regulates levels of genomic methylation. We identified a novel RNA arising from the CEBPA gene locus critical in regulating the local DNA methylation profile. This RNA binds to DNMT1 and prevents CEBPA gene locus methylation. Deep sequencing of transcripts associated with DNMT1 combined with genome-scale methylation and expression profiling extended the generality of this finding to numerous gene loci. Collectively, these results delineate the nature of DNMT1-RNA interactions and suggest strategies for gene selective demethylation of therapeutic targets in disease.

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          Most cited references42

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          A coding-independent function of gene and pseudogene mRNAs regulates tumour biology

          The canonical role of messenger RNA (mRNA) is to deliver protein-coding information to sites of protein synthesis. However, given that microRNAs bind to RNAs, we hypothesized that RNAs possess a biological role in cancer cells that relies upon their ability to compete for microRNA binding and is independent of their protein-coding function. As a paradigm for the protein-coding-independent role of RNAs, we describe the functional relationship between the mRNAs produced by the PTEN tumour suppressor gene and its pseudogene (PTENP1) and the critical consequences of this interaction. We find that PTENP1 is biologically active as determined by its ability to regulate cellular levels of PTEN, and that it can exert a growth-suppressive role. We also show that PTENP1 locus is selectively lost in human cancer. We extend our analysis to other cancer-related genes that possess pseudogenes, such as oncogenic KRAS. Further, we demonstrate that the transcripts of protein coding genes such as PTEN are also biologically active. Together, these findings attribute a novel biological role to expressed pseudogenes, as they can regulate coding gene expression, and reveal a non-coding function for mRNAs.
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            Vienna RNA secondary structure server.

            The Vienna RNA secondary structure server provides a web interface to the most frequently used functions of the Vienna RNA software package for the analysis of RNA secondary structures. It currently offers prediction of secondary structure from a single sequence, prediction of the consensus secondary structure for a set of aligned sequences and the design of sequences that will fold into a predefined structure. All three services can be accessed via the Vienna RNA web server at http://rna.tbi.univie.ac.at/.
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              RNA regulons: coordination of post-transcriptional events.

              Jack Keene (2007)
              Recent findings demonstrate that multiple mRNAs are co-regulated by one or more sequence-specific RNA-binding proteins that orchestrate their splicing, export, stability, localization and translation. These and other observations have given rise to a model in which mRNAs that encode functionally related proteins are coordinately regulated during cell growth and differentiation as post-transcriptional RNA operons or regulons, through a ribonucleoprotein-driven mechanism. Here I describe several recently discovered examples of RNA operons in budding yeast, fruitfly and mammalian cells, and their potential importance in processes such as immune response, oxidative metabolism, stress response, circadian rhythms and disease. I close by considering the evolutionary wiring and rewiring of these combinatorial post-transcriptional gene-expression networks.
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                Author and article information

                Journal
                0410462
                6011
                Nature
                Nature
                Nature
                0028-0836
                1476-4687
                19 November 2013
                09 October 2013
                21 November 2013
                21 May 2014
                : 503
                : 7476
                : 10.1038/nature12598
                Affiliations
                [1 ]Harvard Stem Cell Institute, Harvard Medical School, Boston, MA, 02115, USA
                [2 ]Beth Israel Deaconess Medical Center, Boston, MA, 02115, USA
                [3 ]Policlinico A. Gemelli, Catholic University, School of Medicine and Surgery, Rome, Italy
                [4 ]Cancer Science Institute, National University of Singapore, 117599, Singapore
                [5 ]Department of Stem Cell and Regenerative Biology, Harvard University, 7 Divinity Ave, Cambridge, MA, 02138
                [6 ]Broad Institute of MIT and Harvard, 7 Cambridge Center, Cambridge MA, 02142
                [7 ]Computer Science and Artificial Intelligence Lab, Massachusetts Institute of Technology, 32 Vassar St., Cambridge, MA 02139
                [8 ]University of Michigan, Department of Pathology, Ann Arbor, MI 48109-2200
                [9 ]New England Biolabs, 240 County Road, Ipswich, Massachusetts 01938-2723
                [10 ]Dept of Medicine, Hematology-Oncology, C-620 Weill Cornell Medical College 1300 York Avenue, New York, NY 10021
                Author notes
                [§ ]Contact: Daniel G. Tenen, Center for Life Sciences, 3 Blackfan Circle, Room 437, Boston, MA 02115, Tel: 617-735-2235, FAX: 617-735-2222, daniel.tenen@ 123456nus.edu.sg
                [*]

                These two authors equally contributed to the work;

                Article
                NIHMS517921
                10.1038/nature12598
                3870304
                24107992
                209fbdd7-247d-4008-9fd3-8ada554882ea

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                History
                Funding
                Funded by: National Heart, Lung, and Blood Institute : NHLBI
                Award ID: R01 HL112719 || HL
                Funded by: National Heart, Lung, and Blood Institute : NHLBI
                Award ID: R01 HL056745 || HL
                Funded by: National Cancer Institute : NCI
                Award ID: R01 CA118316 || CA
                Funded by: National Cancer Institute : NCI
                Award ID: P01 CA066996 || CA
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