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C. elegans germ granules sculpt both germline and somatic RNAome
Germ granules are membrane-less organelles essential for small RNA biogenesis and germline development. Among the conserved properties of germ granules is their association with the nuclear membrane. Recent studies demonstrated that LOTUS domain proteins, EGGD-1 and EGGD-2 (also known as MIP-1 and M...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10520050/ https://www.ncbi.nlm.nih.gov/pubmed/37749091 http://dx.doi.org/10.1038/s41467-023-41556-4 |
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author | Price, Ian F. Wagner, Jillian A. Pastore, Benjamin Hertz, Hannah L. Tang, Wen |
author_facet | Price, Ian F. Wagner, Jillian A. Pastore, Benjamin Hertz, Hannah L. Tang, Wen |
author_sort | Price, Ian F. |
collection | PubMed |
description | Germ granules are membrane-less organelles essential for small RNA biogenesis and germline development. Among the conserved properties of germ granules is their association with the nuclear membrane. Recent studies demonstrated that LOTUS domain proteins, EGGD-1 and EGGD-2 (also known as MIP-1 and MIP-2 respectively), promote the formation of perinuclear germ granules in C. elegans. This finding presents a unique opportunity to evaluate the significance of perinuclear localization of germ granules. Here we show that loss of eggd-1 causes the coalescence of germ granules and formation of abnormal cytoplasmic aggregates. Impairment of perinuclear granules affects certain germline classes of small RNAs including Piwi-interacting RNAs. Transcriptome profiling reveals overexpression of spermatogenic and cuticle-related genes in eggd-1 hermaphrodites. We further demonstrate that disruption of germ granules activates HLH-30-mediated transcriptional program in somatic tissues. Collectively, our findings underscore the essential role of EGGD-1 in germ granule organization and reveal an unexpected germ granule-to-soma communication. |
format | Online Article Text |
id | pubmed-10520050 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105200502023-09-27 C. elegans germ granules sculpt both germline and somatic RNAome Price, Ian F. Wagner, Jillian A. Pastore, Benjamin Hertz, Hannah L. Tang, Wen Nat Commun Article Germ granules are membrane-less organelles essential for small RNA biogenesis and germline development. Among the conserved properties of germ granules is their association with the nuclear membrane. Recent studies demonstrated that LOTUS domain proteins, EGGD-1 and EGGD-2 (also known as MIP-1 and MIP-2 respectively), promote the formation of perinuclear germ granules in C. elegans. This finding presents a unique opportunity to evaluate the significance of perinuclear localization of germ granules. Here we show that loss of eggd-1 causes the coalescence of germ granules and formation of abnormal cytoplasmic aggregates. Impairment of perinuclear granules affects certain germline classes of small RNAs including Piwi-interacting RNAs. Transcriptome profiling reveals overexpression of spermatogenic and cuticle-related genes in eggd-1 hermaphrodites. We further demonstrate that disruption of germ granules activates HLH-30-mediated transcriptional program in somatic tissues. Collectively, our findings underscore the essential role of EGGD-1 in germ granule organization and reveal an unexpected germ granule-to-soma communication. Nature Publishing Group UK 2023-09-25 /pmc/articles/PMC10520050/ /pubmed/37749091 http://dx.doi.org/10.1038/s41467-023-41556-4 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Price, Ian F. Wagner, Jillian A. Pastore, Benjamin Hertz, Hannah L. Tang, Wen C. elegans germ granules sculpt both germline and somatic RNAome |
title | C. elegans germ granules sculpt both germline and somatic RNAome |
title_full | C. elegans germ granules sculpt both germline and somatic RNAome |
title_fullStr | C. elegans germ granules sculpt both germline and somatic RNAome |
title_full_unstemmed | C. elegans germ granules sculpt both germline and somatic RNAome |
title_short | C. elegans germ granules sculpt both germline and somatic RNAome |
title_sort | c. elegans germ granules sculpt both germline and somatic rnaome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10520050/ https://www.ncbi.nlm.nih.gov/pubmed/37749091 http://dx.doi.org/10.1038/s41467-023-41556-4 |
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