Cargando…

Phase transitioned nuclear Oskar promotes cell division of Drosophila primordial germ cells

Germ granules are non-membranous ribonucleoprotein granules deemed the hubs for post-transcriptional gene regulation and functionally linked to germ cell fate across species. Little is known about the physical properties of germ granules and how these relate to germ cell function. Here we study two...

Descripción completa

Detalles Bibliográficos
Autores principales: Kistler, Kathryn E, Trcek, Tatjana, Hurd, Thomas R, Chen, Ruoyu, Liang, Feng-Xia, Sall, Joseph, Kato, Masato, Lehmann, Ruth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191285/
https://www.ncbi.nlm.nih.gov/pubmed/30260314
http://dx.doi.org/10.7554/eLife.37949
_version_ 1783363698421661696
author Kistler, Kathryn E
Trcek, Tatjana
Hurd, Thomas R
Chen, Ruoyu
Liang, Feng-Xia
Sall, Joseph
Kato, Masato
Lehmann, Ruth
author_facet Kistler, Kathryn E
Trcek, Tatjana
Hurd, Thomas R
Chen, Ruoyu
Liang, Feng-Xia
Sall, Joseph
Kato, Masato
Lehmann, Ruth
author_sort Kistler, Kathryn E
collection PubMed
description Germ granules are non-membranous ribonucleoprotein granules deemed the hubs for post-transcriptional gene regulation and functionally linked to germ cell fate across species. Little is known about the physical properties of germ granules and how these relate to germ cell function. Here we study two types of germ granules in the Drosophila embryo: cytoplasmic germ granules that instruct primordial germ cells (PGCs) formation and nuclear germ granules within early PGCs with unknown function. We show that cytoplasmic and nuclear germ granules are phase transitioned condensates nucleated by Oskar protein that display liquid as well as hydrogel-like properties. Focusing on nuclear granules, we find that Oskar drives their formation in heterologous cell systems. Multiple, independent Oskar protein domains synergize to promote granule phase separation. Deletion of Oskar’s nuclear localization sequence specifically ablates nuclear granules in cell systems. In the embryo, nuclear germ granules promote germ cell divisions thereby increasing PGC number for the next generation.
format Online
Article
Text
id pubmed-6191285
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-61912852018-10-21 Phase transitioned nuclear Oskar promotes cell division of Drosophila primordial germ cells Kistler, Kathryn E Trcek, Tatjana Hurd, Thomas R Chen, Ruoyu Liang, Feng-Xia Sall, Joseph Kato, Masato Lehmann, Ruth eLife Cell Biology Germ granules are non-membranous ribonucleoprotein granules deemed the hubs for post-transcriptional gene regulation and functionally linked to germ cell fate across species. Little is known about the physical properties of germ granules and how these relate to germ cell function. Here we study two types of germ granules in the Drosophila embryo: cytoplasmic germ granules that instruct primordial germ cells (PGCs) formation and nuclear germ granules within early PGCs with unknown function. We show that cytoplasmic and nuclear germ granules are phase transitioned condensates nucleated by Oskar protein that display liquid as well as hydrogel-like properties. Focusing on nuclear granules, we find that Oskar drives their formation in heterologous cell systems. Multiple, independent Oskar protein domains synergize to promote granule phase separation. Deletion of Oskar’s nuclear localization sequence specifically ablates nuclear granules in cell systems. In the embryo, nuclear germ granules promote germ cell divisions thereby increasing PGC number for the next generation. eLife Sciences Publications, Ltd 2018-09-27 /pmc/articles/PMC6191285/ /pubmed/30260314 http://dx.doi.org/10.7554/eLife.37949 Text en © 2018, Kistler et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Kistler, Kathryn E
Trcek, Tatjana
Hurd, Thomas R
Chen, Ruoyu
Liang, Feng-Xia
Sall, Joseph
Kato, Masato
Lehmann, Ruth
Phase transitioned nuclear Oskar promotes cell division of Drosophila primordial germ cells
title Phase transitioned nuclear Oskar promotes cell division of Drosophila primordial germ cells
title_full Phase transitioned nuclear Oskar promotes cell division of Drosophila primordial germ cells
title_fullStr Phase transitioned nuclear Oskar promotes cell division of Drosophila primordial germ cells
title_full_unstemmed Phase transitioned nuclear Oskar promotes cell division of Drosophila primordial germ cells
title_short Phase transitioned nuclear Oskar promotes cell division of Drosophila primordial germ cells
title_sort phase transitioned nuclear oskar promotes cell division of drosophila primordial germ cells
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191285/
https://www.ncbi.nlm.nih.gov/pubmed/30260314
http://dx.doi.org/10.7554/eLife.37949
work_keys_str_mv AT kistlerkathryne phasetransitionednuclearoskarpromotescelldivisionofdrosophilaprimordialgermcells
AT trcektatjana phasetransitionednuclearoskarpromotescelldivisionofdrosophilaprimordialgermcells
AT hurdthomasr phasetransitionednuclearoskarpromotescelldivisionofdrosophilaprimordialgermcells
AT chenruoyu phasetransitionednuclearoskarpromotescelldivisionofdrosophilaprimordialgermcells
AT liangfengxia phasetransitionednuclearoskarpromotescelldivisionofdrosophilaprimordialgermcells
AT salljoseph phasetransitionednuclearoskarpromotescelldivisionofdrosophilaprimordialgermcells
AT katomasato phasetransitionednuclearoskarpromotescelldivisionofdrosophilaprimordialgermcells
AT lehmannruth phasetransitionednuclearoskarpromotescelldivisionofdrosophilaprimordialgermcells