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Topological organization and dynamic regulation of human tRNA genes during macrophage differentiation

BACKGROUND: The human genome is hierarchically organized into local and long-range structures that help shape cell-type-specific transcription patterns. Transfer RNA (tRNA) genes (tDNAs), which are transcribed by RNA polymerase III (RNAPIII) and encode RNA molecules responsible for translation, are...

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Autores principales: Van Bortle, Kevin, Phanstiel, Douglas H., Snyder, Michael P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607496/
https://www.ncbi.nlm.nih.gov/pubmed/28931413
http://dx.doi.org/10.1186/s13059-017-1310-3
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author Van Bortle, Kevin
Phanstiel, Douglas H.
Snyder, Michael P.
author_facet Van Bortle, Kevin
Phanstiel, Douglas H.
Snyder, Michael P.
author_sort Van Bortle, Kevin
collection PubMed
description BACKGROUND: The human genome is hierarchically organized into local and long-range structures that help shape cell-type-specific transcription patterns. Transfer RNA (tRNA) genes (tDNAs), which are transcribed by RNA polymerase III (RNAPIII) and encode RNA molecules responsible for translation, are dispersed throughout the genome and, in many cases, linearly organized into genomic clusters with other tDNAs. Whether the location and three-dimensional organization of tDNAs contribute to the activity of these genes has remained difficult to address, due in part to unique challenges related to tRNA sequencing. We therefore devised integrated tDNA expression profiling, a method that combines RNAPIII mapping with biotin-capture of nascent tRNAs. We apply this method to the study of dynamic tRNA gene regulation during macrophage development and further integrate these data with high-resolution maps of 3D chromatin structure. RESULTS: Integrated tDNA expression profiling reveals domain-level and loop-based organization of tRNA gene transcription during cellular differentiation. tRNA genes connected by DNA loops, which are proximal to CTCF binding sites and expressed at elevated levels compared to non-loop tDNAs, change coordinately with tDNAs and protein-coding genes at distal ends of interactions mapped by in situ Hi-C. We find that downregulated tRNA genes are specifically marked by enhanced promoter-proximal binding of MAF1, a transcriptional repressor of RNAPIII activity, altogether revealing multiple levels of tDNA regulation during cellular differentiation. CONCLUSIONS: We present evidence of both local and coordinated long-range regulation of human tDNA expression, suggesting the location and organization of tRNA genes contribute to dynamic tDNA activity during macrophage development. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-017-1310-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-56074962017-09-24 Topological organization and dynamic regulation of human tRNA genes during macrophage differentiation Van Bortle, Kevin Phanstiel, Douglas H. Snyder, Michael P. Genome Biol Research BACKGROUND: The human genome is hierarchically organized into local and long-range structures that help shape cell-type-specific transcription patterns. Transfer RNA (tRNA) genes (tDNAs), which are transcribed by RNA polymerase III (RNAPIII) and encode RNA molecules responsible for translation, are dispersed throughout the genome and, in many cases, linearly organized into genomic clusters with other tDNAs. Whether the location and three-dimensional organization of tDNAs contribute to the activity of these genes has remained difficult to address, due in part to unique challenges related to tRNA sequencing. We therefore devised integrated tDNA expression profiling, a method that combines RNAPIII mapping with biotin-capture of nascent tRNAs. We apply this method to the study of dynamic tRNA gene regulation during macrophage development and further integrate these data with high-resolution maps of 3D chromatin structure. RESULTS: Integrated tDNA expression profiling reveals domain-level and loop-based organization of tRNA gene transcription during cellular differentiation. tRNA genes connected by DNA loops, which are proximal to CTCF binding sites and expressed at elevated levels compared to non-loop tDNAs, change coordinately with tDNAs and protein-coding genes at distal ends of interactions mapped by in situ Hi-C. We find that downregulated tRNA genes are specifically marked by enhanced promoter-proximal binding of MAF1, a transcriptional repressor of RNAPIII activity, altogether revealing multiple levels of tDNA regulation during cellular differentiation. CONCLUSIONS: We present evidence of both local and coordinated long-range regulation of human tDNA expression, suggesting the location and organization of tRNA genes contribute to dynamic tDNA activity during macrophage development. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-017-1310-3) contains supplementary material, which is available to authorized users. BioMed Central 2017-09-20 /pmc/articles/PMC5607496/ /pubmed/28931413 http://dx.doi.org/10.1186/s13059-017-1310-3 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Van Bortle, Kevin
Phanstiel, Douglas H.
Snyder, Michael P.
Topological organization and dynamic regulation of human tRNA genes during macrophage differentiation
title Topological organization and dynamic regulation of human tRNA genes during macrophage differentiation
title_full Topological organization and dynamic regulation of human tRNA genes during macrophage differentiation
title_fullStr Topological organization and dynamic regulation of human tRNA genes during macrophage differentiation
title_full_unstemmed Topological organization and dynamic regulation of human tRNA genes during macrophage differentiation
title_short Topological organization and dynamic regulation of human tRNA genes during macrophage differentiation
title_sort topological organization and dynamic regulation of human trna genes during macrophage differentiation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607496/
https://www.ncbi.nlm.nih.gov/pubmed/28931413
http://dx.doi.org/10.1186/s13059-017-1310-3
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