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The molecular dynamics of long noncoding RNA control of transcription in PTEN and its pseudogene.


ABSTRACT: RNA has been found to interact with chromatin and modulate gene transcription. In human cells, little is known about how long noncoding RNAs (lncRNAs) interact with target loci in the context of chromatin. We find here, using the phosphatase and tensin homolog (PTEN) pseudogene as a model system, that antisense lncRNAs interact first with a 5' UTR-containing promoter-spanning transcript, which is then followed by the recruitment of DNA methyltransferase 3a (DNMT3a), ultimately resulting in the transcriptional and epigenetic control of gene expression. Moreover, we find that the lncRNA and promoter-spanning transcript interaction are based on a combination of structural and sequence components of the antisense lncRNA. These observations suggest, on the basis of this one example, that evolutionary pressures may be placed on RNA structure more so than sequence conservation. Collectively, the observations presented here suggest a much more complex and vibrant RNA regulatory world may be operative in the regulation of gene expression.

SUBMITTER: Lister N 

PROVIDER: S-EPMC5603994 | biostudies-literature | 2017 Sep

REPOSITORIES: biostudies-literature

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The molecular dynamics of long noncoding RNA control of transcription in PTEN and its pseudogene.

Lister Nicholas N   Shevchenko Galina G   Walshe James L JL   Groen Jessica J   Johnsson Per P   Vidarsdóttir Linda L   Grander Dan D   Ataide Sandro F SF   Morris Kevin V KV  

Proceedings of the National Academy of Sciences of the United States of America 20170828 37


RNA has been found to interact with chromatin and modulate gene transcription. In human cells, little is known about how long noncoding RNAs (lncRNAs) interact with target loci in the context of chromatin. We find here, using the phosphatase and tensin homolog (PTEN) pseudogene as a model system, that antisense lncRNAs interact first with a 5' UTR-containing promoter-spanning transcript, which is then followed by the recruitment of DNA methyltransferase 3a (DNMT3a), ultimately resulting in the t  ...[more]

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