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The Tug1 lncRNA locus is essential for male fertility

BACKGROUND: Several long noncoding RNAs (lncRNAs) have been shown to function as components of molecular machines that play fundamental roles in biology. While the number of annotated lncRNAs in mammalian genomes has greatly expanded, studying lncRNA function has been a challenge due to their divers...

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Autores principales: Lewandowski, Jordan P., Dumbović, Gabrijela, Watson, Audrey R., Hwang, Taeyoung, Jacobs-Palmer, Emily, Chang, Nydia, Much, Christian, Turner, Kyle M., Kirby, Christopher, Rubinstein, Nimrod D., Groff, Abigail F., Liapis, Steve C., Gerhardinger, Chiara, Bester, Assaf, Pandolfi, Pier Paolo, Clohessy, John G., Hoekstra, Hopi E., Sauvageau, Martin, Rinn, John L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7487648/
https://www.ncbi.nlm.nih.gov/pubmed/32894169
http://dx.doi.org/10.1186/s13059-020-02081-5
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author Lewandowski, Jordan P.
Dumbović, Gabrijela
Watson, Audrey R.
Hwang, Taeyoung
Jacobs-Palmer, Emily
Chang, Nydia
Much, Christian
Turner, Kyle M.
Kirby, Christopher
Rubinstein, Nimrod D.
Groff, Abigail F.
Liapis, Steve C.
Gerhardinger, Chiara
Bester, Assaf
Pandolfi, Pier Paolo
Clohessy, John G.
Hoekstra, Hopi E.
Sauvageau, Martin
Rinn, John L.
author_facet Lewandowski, Jordan P.
Dumbović, Gabrijela
Watson, Audrey R.
Hwang, Taeyoung
Jacobs-Palmer, Emily
Chang, Nydia
Much, Christian
Turner, Kyle M.
Kirby, Christopher
Rubinstein, Nimrod D.
Groff, Abigail F.
Liapis, Steve C.
Gerhardinger, Chiara
Bester, Assaf
Pandolfi, Pier Paolo
Clohessy, John G.
Hoekstra, Hopi E.
Sauvageau, Martin
Rinn, John L.
author_sort Lewandowski, Jordan P.
collection PubMed
description BACKGROUND: Several long noncoding RNAs (lncRNAs) have been shown to function as components of molecular machines that play fundamental roles in biology. While the number of annotated lncRNAs in mammalian genomes has greatly expanded, studying lncRNA function has been a challenge due to their diverse biological roles and because lncRNA loci can contain multiple molecular modes that may exert function. RESULTS: We previously generated and characterized a cohort of 20 lncRNA loci knockout mice. Here, we extend this initial study and provide a more detailed analysis of the highly conserved lncRNA locus, taurine-upregulated gene 1 (Tug1). We report that Tug1-knockout male mice are sterile with underlying defects including a low number of sperm and abnormal sperm morphology. Because lncRNA loci can contain multiple modes of action, we wanted to determine which, if any, potential elements contained in the Tug1 genomic region have any activity. Using engineered mouse models and cell-based assays, we provide evidence that the Tug1 locus harbors two distinct noncoding regulatory activities, as a cis-DNA repressor that regulates neighboring genes and as a lncRNA that can regulate genes by a trans-based function. We also show that Tug1 contains an evolutionary conserved open reading frame that when overexpressed produces a stable protein which impacts mitochondrial membrane potential, suggesting a potential third coding function. CONCLUSIONS: Our results reveal an essential role for the Tug1 locus in male fertility and uncover evidence for distinct molecular modes in the Tug1 locus, thus highlighting the complexity present at lncRNA loci.
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spelling pubmed-74876482020-09-15 The Tug1 lncRNA locus is essential for male fertility Lewandowski, Jordan P. Dumbović, Gabrijela Watson, Audrey R. Hwang, Taeyoung Jacobs-Palmer, Emily Chang, Nydia Much, Christian Turner, Kyle M. Kirby, Christopher Rubinstein, Nimrod D. Groff, Abigail F. Liapis, Steve C. Gerhardinger, Chiara Bester, Assaf Pandolfi, Pier Paolo Clohessy, John G. Hoekstra, Hopi E. Sauvageau, Martin Rinn, John L. Genome Biol Research BACKGROUND: Several long noncoding RNAs (lncRNAs) have been shown to function as components of molecular machines that play fundamental roles in biology. While the number of annotated lncRNAs in mammalian genomes has greatly expanded, studying lncRNA function has been a challenge due to their diverse biological roles and because lncRNA loci can contain multiple molecular modes that may exert function. RESULTS: We previously generated and characterized a cohort of 20 lncRNA loci knockout mice. Here, we extend this initial study and provide a more detailed analysis of the highly conserved lncRNA locus, taurine-upregulated gene 1 (Tug1). We report that Tug1-knockout male mice are sterile with underlying defects including a low number of sperm and abnormal sperm morphology. Because lncRNA loci can contain multiple modes of action, we wanted to determine which, if any, potential elements contained in the Tug1 genomic region have any activity. Using engineered mouse models and cell-based assays, we provide evidence that the Tug1 locus harbors two distinct noncoding regulatory activities, as a cis-DNA repressor that regulates neighboring genes and as a lncRNA that can regulate genes by a trans-based function. We also show that Tug1 contains an evolutionary conserved open reading frame that when overexpressed produces a stable protein which impacts mitochondrial membrane potential, suggesting a potential third coding function. CONCLUSIONS: Our results reveal an essential role for the Tug1 locus in male fertility and uncover evidence for distinct molecular modes in the Tug1 locus, thus highlighting the complexity present at lncRNA loci. BioMed Central 2020-09-07 /pmc/articles/PMC7487648/ /pubmed/32894169 http://dx.doi.org/10.1186/s13059-020-02081-5 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research
Lewandowski, Jordan P.
Dumbović, Gabrijela
Watson, Audrey R.
Hwang, Taeyoung
Jacobs-Palmer, Emily
Chang, Nydia
Much, Christian
Turner, Kyle M.
Kirby, Christopher
Rubinstein, Nimrod D.
Groff, Abigail F.
Liapis, Steve C.
Gerhardinger, Chiara
Bester, Assaf
Pandolfi, Pier Paolo
Clohessy, John G.
Hoekstra, Hopi E.
Sauvageau, Martin
Rinn, John L.
The Tug1 lncRNA locus is essential for male fertility
title The Tug1 lncRNA locus is essential for male fertility
title_full The Tug1 lncRNA locus is essential for male fertility
title_fullStr The Tug1 lncRNA locus is essential for male fertility
title_full_unstemmed The Tug1 lncRNA locus is essential for male fertility
title_short The Tug1 lncRNA locus is essential for male fertility
title_sort tug1 lncrna locus is essential for male fertility
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7487648/
https://www.ncbi.nlm.nih.gov/pubmed/32894169
http://dx.doi.org/10.1186/s13059-020-02081-5
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