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      Psip1/p52 regulates posterior Hoxa genes through activation of lncRNA Hottip

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          Abstract

          Long noncoding RNAs (lncRNAs) have been implicated in various biological functions including the regulation of gene expression, however, the functionality of lncRNAs is not clearly understood and conflicting conclusions have often been reached when comparing different methods to investigate them. Moreover, little is known about the upstream regulation of lncRNAs. Here we show that the short isoform (p52) of a transcriptional co-activator—PC4 and SF2 interacting protein (Psip1), which is known to be involved in linking transcription to RNA processing, specifically regulates the expression of the lncRNA Hottip–located at the 5’ end of the Hoxa locus. Using both knockdown and knockout approaches we show that Hottip expression is required for activation of the 5’ Hoxa genes ( Hoxa13 and Hoxa10/11) and for retaining Mll1 at the 5’ end of Hoxa. Moreover, we demonstrate that artificially inducing Hottip expression is sufficient to activate the 5’ Hoxa genes and that Hottip RNA binds to the 5’ end of Hoxa. By engineering premature transcription termination, we show that it is the Hottip lncRNA molecule itself, not just Hottip transcription that is required to maintains active expression of posterior Hox genes. Our data show a direct role for a lncRNA molecule in regulating the expression of developmentally-regulated mRNA genes in cis.

          Author summary

          Long noncoding RNAs (lncRNAs) have been implicated in various biological functions including regulation of gene expression. However, the mechanism through which they regulate gene expression is not clearly understood. Here we show that a transcriptional co activator—Psip1 specifically regulates the expression of the lncRNA Hottip. Moreover, using multiple approaches, including lncRNA depletion, genetic manipulation of Hottip locus, transcriptional activation and premature termination of lncRNA transcript along with RNA localization, we demonstrate that Hottip lncRNA regulates expression of neighbouring Hoxa genes.

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          Most cited references38

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          The evolution of lncRNA repertoires and expression patterns in tetrapods.

          Only a very small fraction of long noncoding RNAs (lncRNAs) are well characterized. The evolutionary history of lncRNAs can provide insights into their functionality, but the absence of lncRNA annotations in non-model organisms has precluded comparative analyses. Here we present a large-scale evolutionary study of lncRNA repertoires and expression patterns, in 11 tetrapod species. We identify approximately 11,000 primate-specific lncRNAs and 2,500 highly conserved lncRNAs, including approximately 400 genes that are likely to have originated more than 300 million years ago. We find that lncRNAs, in particular ancient ones, are in general actively regulated and may function predominantly in embryonic development. Most lncRNAs evolve rapidly in terms of sequence and expression levels, but tissue specificities are often conserved. We compared expression patterns of homologous lncRNA and protein-coding families across tetrapods to reconstruct an evolutionarily conserved co-expression network. This network suggests potential functions for lncRNAs in fundamental processes such as spermatogenesis and synaptic transmission, but also in more specific mechanisms such as placenta development through microRNA production.
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            The H19 lincRNA is a developmental reservoir of miR-675 which suppresses growth and Igf1r

            The H19 large intergenic noncoding RNA (lincRNA) is one of the most highly abundant and conserved transcripts in mammalian development, being expressed in both embryonic and extraembryonic cell lineages, yet its physiological function is unknown. Here we show that miR-675, a microRNA (miRNA) embedded within H19’s first exon, is expressed exclusively in the placenta from the gestational time point when placental growth normally ceases, and placentas that lack H19 continue to grow. Overexpression of miR-675 in a range of embryonic and extraembryonic cell lines results in their reduced proliferation; targets of the miRNA are upregulated in the H19 null placenta, including the growth promoting Insulin-like growth factor 1 receptor (Igf1r). Moreover, the excision of miR-675 from H19 is dynamically regulated by the stress response RNA binding protein HuR. These results suggest that H19’s main physiological role is in limiting growth of the placenta prior to birth, by regulated processing of miR-675. The controlled release of miR-675 from H19 may also allow rapid inhibition of cell proliferation in response to cellular stress or oncogenic signals.
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              Transcribed enhancers lead waves of coordinated transcription in transitioning mammalian cells.

              Although it is generally accepted that cellular differentiation requires changes to transcriptional networks, dynamic regulation of promoters and enhancers at specific sets of genes has not been previously studied en masse. Exploiting the fact that active promoters and enhancers are transcribed, we simultaneously measured their activity in 19 human and 14 mouse time courses covering a wide range of cell types and biological stimuli. Enhancer RNAs, then messenger RNAs encoding transcription factors, dominated the earliest responses. Binding sites for key lineage transcription factors were simultaneously overrepresented in enhancers and promoters active in each cellular system. Our data support a highly generalizable model in which enhancer transcription is the earliest event in successive waves of transcriptional change during cellular differentiation or activation. Copyright © 2015, American Association for the Advancement of Science.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS Genet
                PLoS Genet
                plos
                plosgen
                PLoS Genetics
                Public Library of Science (San Francisco, CA USA )
                1553-7390
                1553-7404
                6 April 2017
                April 2017
                : 13
                : 4
                : e1006677
                Affiliations
                [1 ]MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine at University of Edinburgh, Edinburgh, United Kingdom
                [2 ]School of biological sciences, University of Essex, Colchester, United Kingdom
                Stanford University School of Medicine, UNITED STATES
                Author notes

                The authors have declared that no competing interests exist.

                • Conceptualization: MMP WAB.

                • Data curation: MMP GRG.

                • Formal analysis: MMP GRG.

                • Funding acquisition: MMP WAB.

                • Investigation: MMP FM.

                • Methodology: MMP GCAT SB HB AJW.

                • Project administration: MMP WAB.

                • Supervision: MMP.

                • Validation: MMP.

                • Visualization: MMP WAB.

                • Writing – original draft: MMP.

                • Writing – review & editing: MMP WAB.

                Author information
                http://orcid.org/0000-0002-3370-8326
                http://orcid.org/0000-0002-0653-2070
                http://orcid.org/0000-0001-6660-7735
                Article
                PGENETICS-D-16-01455
                10.1371/journal.pgen.1006677
                5383017
                28384324
                a83d46d6-8a50-4097-b886-304ec5cea815
                © 2017 Pradeepa et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 5 July 2016
                : 9 March 2017
                Page count
                Figures: 5, Tables: 0, Pages: 18
                Funding
                Funded by: Medical Research Council (GB)
                Award Recipient :
                This work was supported by a unit programme grant – 4127527202 from the Medical Research Council, UK. http://www.mrc.ac.uk/. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and life sciences
                Biochemistry
                Nucleic acids
                RNA
                Non-coding RNA
                Long non-coding RNAs
                Biology and Life Sciences
                Genetics
                Gene Expression
                Biology and Life Sciences
                Genetics
                Genetic Loci
                Biology and Life Sciences
                Biochemistry
                Proteins
                Protein Domains
                Homeobox
                Biology and Life Sciences
                Genetics
                Genomics
                Animal Genomics
                Mammalian Genomics
                Biology and Life Sciences
                Genetics
                Gene Expression
                Gene Regulation
                Biology and Life Sciences
                Developmental Biology
                Embryology
                Embryos
                Biology and life sciences
                Genetics
                Gene expression
                DNA transcription
                Custom metadata
                All data are available from GEO using the following URLs: https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GPL13276, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE95064

                Genetics
                Genetics

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