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      Locked nucleic acids (LNAs) reveal sequence requirements and kinetics of Xist RNA localization to the X chromosome.

      Proceedings of the National Academy of Sciences of the United States of America

      RNA, Long Noncoding, Animals, Histones, Polycomb-Group Proteins, metabolism, RNA Stability, Mice, Epigenesis, Genetic, RNA, Untranslated, genetics, Gene Knockdown Techniques, X Chromosome, Repressor Proteins, Kinetics, physiology, Cell Line, Transformed

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          Abstract

          A large fraction of the mammalian genome is transcribed into long noncoding RNAs. The RNAs remain largely uncharacterized as the field awaits new technologies to aid functional analysis. Here, we describe a unique use of locked nucleic acids (LNAs) for studying nuclear long noncoding RNA, an RNA subclass that has been less amenable to traditional knockdown techniques. We target LNAs at Xist RNA and show displacement from the X chromosome with fast kinetics. Xist transcript stability is not affected. By targeting different Xist regions, we identify a localization domain and show that polycomb repressive complex 2 (PRC2) is displaced together with Xist. Thus, PRC2 depends on RNA for both initial targeting to and stable association with chromatin. H3K27-trimethyl marks and gene silencing remain stable. Time-course analysis of RNA relocalization suggests that Xist and PRC2 bind to different regions of the X at the same time but do not reach saturating levels immediately. Thus, LNAs provide a tool for studying an emerging class of regulatory RNA and offer a window of opportunity to target epigenetic modifications with possible therapeutic applications.

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          Author and article information

          Journal
          21135235
          3009817
          10.1073/pnas.1009785107

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