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We are analyzing https://link.springer.com/article/10.1186/s13059-016-1079-9.

Title:
Extensive RNA editing and splicing increase immune self-representation diversity in medullary thymic epithelial cells | Genome Biology
Description:
Background In order to become functionally competent but harmless mediators of the immune system, T cells undergo a strict educational program in the thymus, where they learn to discriminate between self and non-self. This educational program is, to a large extent, mediated by medullary thymic epithelial cells that have a unique capacity to express, and subsequently present, a large fraction of body antigens. While the scope of promiscuously expressed genes by medullary thymic epithelial cells is well-established, relatively little is known about the expression of variants that are generated by co-transcriptional and post-transcriptional processes. Results Our study reveals that in comparison to other cell types, medullary thymic epithelial cells display significantly higher levels of alternative splicing, as well as A-to-I and C-to-U RNA editing, which thereby further expand the diversity of their self-antigen repertoire. Interestingly, Aire, the key mediator of promiscuous gene expression in these cells, plays a limited role in the regulation of these transcriptional processes. Conclusions Our results highlight RNA processing as another layer by which the immune system assures a comprehensive self-representation in the thymus which is required for the establishment of self-tolerance and prevention of autoimmunity.
Website Age:
28 years and 1 months (reg. 1997-05-29).

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  • Science
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Custom-built

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🌠 Phenomenal Traffic: 5M - 10M visitors per month


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Keywords {πŸ”}

mtecs, pubmed, editing, article, google, scholar, tissues, gene, expressed, cas, expression, sites, rna, genes, cells, reads, central, high, number, tissue, levels, fig, analysis, cell, sample, genome, thymic, splice, splicing, epithelial, brain, tra, examined, ctou, rnaediting, rate, junctions, level, data, results, types, rnaseq, mtechi, mature, population, edited, alternative, aire, protein, thymus,

Topics {βœ’οΈ}

poly-a-selected transcriptome libraries central t-cell tolerance tissue-restricted rna-splicing products article download pdf aire-dependent tissue-restricted antigen single-cell genomics reveal article danan-gotthold specific pathogen-free conditions high-throughput sequencing data replicate rna-seq data thymic medulla rna-editing site conservation mtecs vis-Γ -vis thymic epithelial cells paris-descartes ethical committee escaped central tolerance rna-seq read uniquely tissue-specific gene signature central immunological tolerance full size image low mhc-ii [mteclo] central tolerance mechanisms high mhc-ii [mtechi] tissue-restricted splice junctions mhc-ii low mtecs mhc-ii high mtecs single transcriptional regulator extensive rna processing global rna-editing rate tissue-restricted splice variants full access aire-deficient mtecs displayed extensive rna editing unique hyper-editing sites european research council tissue-restricted antigen genes rna-seq datasets obtained high rna-editing levels tissue-specific splice variants apobec-1-mediated rna editing highest rna-editing capacity highest rna-editing levels high rna-editing rate transcriptome-wide regulation synonymous rna-editing sites privacy choices/manage cookies global transcriptome analysis white rectangle denotes high-throughput sequencing high rna-editing level

Schema {πŸ—ΊοΈ}

WebPage:
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         headline:Extensive RNA editing and splicing increase immune self-representation diversity in medullary thymic epithelial cells
         description:In order to become functionally competent but harmless mediators of the immune system, T cells undergo a strict educational program in the thymus, where they learn to discriminate between self and non-self. This educational program is, to a large extent, mediated by medullary thymic epithelial cells that have a unique capacity to express, and subsequently present, a large fraction of body antigens. While the scope of promiscuously expressed genes by medullary thymic epithelial cells is well-established, relatively little is known about the expression of variants that are generated by co-transcriptional and post-transcriptional processes. Our study reveals that in comparison to other cell types, medullary thymic epithelial cells display significantly higher levels of alternative splicing, as well as A-to-I and C-to-U RNA editing, which thereby further expand the diversity of their self-antigen repertoire. Interestingly, Aire, the key mediator of promiscuous gene expression in these cells, plays a limited role in the regulation of these transcriptional processes. Our results highlight RNA processing as another layer by which the immune system assures a comprehensive self-representation in the thymus which is required for the establishment of self-tolerance and prevention of autoimmunity.
         datePublished:2016-10-24T00:00:00Z
         dateModified:2016-10-24T00:00:00Z
         pageStart:1
         pageEnd:13
         license:http://creativecommons.org/publicdomain/zero/1.0/
         sameAs:https://doi.org/10.1186/s13059-016-1079-9
         keywords:
            Medullary thymic epithelial cells (mTECs)
            Thymus
            Alternative splicing
            RNA editing
            RNA sequencing
            Self-tolerance
            Animal Genetics and Genomics
            Human Genetics
            Plant Genetics and Genomics
            Microbial Genetics and Genomics
            Bioinformatics
            Evolutionary Biology
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            issn:
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         author:
               name:Miri Danan-Gotthold
               url:http://orcid.org/0000-0002-6819-6308
               affiliation:
                     name:Bar-Ilan University
                     address:
                        name:The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel
                        type:PostalAddress
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               name:Clotilde Guyon
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                     address:
                        name:Department of Infection Immunity and Inflammation, Cochin Institute, Paris, France
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Matthieu Giraud
               affiliation:
                     name:Department of Infection Immunity and Inflammation, Cochin Institute
                     address:
                        name:Department of Infection Immunity and Inflammation, Cochin Institute, Paris, France
                        type:PostalAddress
                     type:Organization
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               name:Erez Y. Levanon
               affiliation:
                     name:Bar-Ilan University
                     address:
                        name:The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel
                        type:PostalAddress
                     type:Organization
               email:[email protected]
               type:Person
               name:Jakub Abramson
               affiliation:
                     name:Weizmann Institute of Science
                     address:
                        name:Department of Immunology, Weizmann Institute of Science, Rehovot, Israel
                        type:PostalAddress
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ScholarlyArticle:
      headline:Extensive RNA editing and splicing increase immune self-representation diversity in medullary thymic epithelial cells
      description:In order to become functionally competent but harmless mediators of the immune system, T cells undergo a strict educational program in the thymus, where they learn to discriminate between self and non-self. This educational program is, to a large extent, mediated by medullary thymic epithelial cells that have a unique capacity to express, and subsequently present, a large fraction of body antigens. While the scope of promiscuously expressed genes by medullary thymic epithelial cells is well-established, relatively little is known about the expression of variants that are generated by co-transcriptional and post-transcriptional processes. Our study reveals that in comparison to other cell types, medullary thymic epithelial cells display significantly higher levels of alternative splicing, as well as A-to-I and C-to-U RNA editing, which thereby further expand the diversity of their self-antigen repertoire. Interestingly, Aire, the key mediator of promiscuous gene expression in these cells, plays a limited role in the regulation of these transcriptional processes. Our results highlight RNA processing as another layer by which the immune system assures a comprehensive self-representation in the thymus which is required for the establishment of self-tolerance and prevention of autoimmunity.
      datePublished:2016-10-24T00:00:00Z
      dateModified:2016-10-24T00:00:00Z
      pageStart:1
      pageEnd:13
      license:http://creativecommons.org/publicdomain/zero/1.0/
      sameAs:https://doi.org/10.1186/s13059-016-1079-9
      keywords:
         Medullary thymic epithelial cells (mTECs)
         Thymus
         Alternative splicing
         RNA editing
         RNA sequencing
         Self-tolerance
         Animal Genetics and Genomics
         Human Genetics
         Plant Genetics and Genomics
         Microbial Genetics and Genomics
         Bioinformatics
         Evolutionary Biology
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         name:BioMed Central
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            type:ImageObject
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      author:
            name:Miri Danan-Gotthold
            url:http://orcid.org/0000-0002-6819-6308
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                  address:
                     name:The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Clotilde Guyon
            affiliation:
                  name:Department of Infection Immunity and Inflammation, Cochin Institute
                  address:
                     name:Department of Infection Immunity and Inflammation, Cochin Institute, Paris, France
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Matthieu Giraud
            affiliation:
                  name:Department of Infection Immunity and Inflammation, Cochin Institute
                  address:
                     name:Department of Infection Immunity and Inflammation, Cochin Institute, Paris, France
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Erez Y. Levanon
            affiliation:
                  name:Bar-Ilan University
                  address:
                     name:The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel
                     type:PostalAddress
                  type:Organization
            email:[email protected]
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            name:Jakub Abramson
            affiliation:
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                  address:
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      address:
         name:Department of Infection Immunity and Inflammation, Cochin Institute, Paris, France
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      name:Department of Infection Immunity and Inflammation, Cochin Institute
      address:
         name:Department of Infection Immunity and Inflammation, Cochin Institute, Paris, France
         type:PostalAddress
      name:Bar-Ilan University
      address:
         name:The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel
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      url:http://orcid.org/0000-0002-6819-6308
      affiliation:
            name:Bar-Ilan University
            address:
               name:The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel
               type:PostalAddress
            type:Organization
      name:Clotilde Guyon
      affiliation:
            name:Department of Infection Immunity and Inflammation, Cochin Institute
            address:
               name:Department of Infection Immunity and Inflammation, Cochin Institute, Paris, France
               type:PostalAddress
            type:Organization
      name:Matthieu Giraud
      affiliation:
            name:Department of Infection Immunity and Inflammation, Cochin Institute
            address:
               name:Department of Infection Immunity and Inflammation, Cochin Institute, Paris, France
               type:PostalAddress
            type:Organization
      name:Erez Y. Levanon
      affiliation:
            name:Bar-Ilan University
            address:
               name:The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel
               type:PostalAddress
            type:Organization
      email:[email protected]
      name:Jakub Abramson
      affiliation:
            name:Weizmann Institute of Science
            address:
               name:Department of Immunology, Weizmann Institute of Science, Rehovot, Israel
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel
      name:Department of Infection Immunity and Inflammation, Cochin Institute, Paris, France
      name:Department of Infection Immunity and Inflammation, Cochin Institute, Paris, France
      name:The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel
      name:Department of Immunology, Weizmann Institute of Science, Rehovot, Israel

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