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Component analysis of nucleolar protein compartments using Xenopus laevis oocytes
The nucleolus is a multi‐compartment, non‐membrane‐bound organelle within the nucleus. Nucleolar assembly is influenced by proteins capable of phase separation. Xenopus laevis oocytes contain hundreds of large nucleoli that provide experimental access for nucleoli that is unavailable in other system...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9474603/ https://www.ncbi.nlm.nih.gov/pubmed/35607824 http://dx.doi.org/10.1111/dgd.12794 |
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author | Lavering, Emily D. Petros, Irini N. Weeks, Daniel L. |
author_facet | Lavering, Emily D. Petros, Irini N. Weeks, Daniel L. |
author_sort | Lavering, Emily D. |
collection | PubMed |
description | The nucleolus is a multi‐compartment, non‐membrane‐bound organelle within the nucleus. Nucleolar assembly is influenced by proteins capable of phase separation. Xenopus laevis oocytes contain hundreds of large nucleoli that provide experimental access for nucleoli that is unavailable in other systems. Here we detail methods to streamline the in vivo analysis of the compartmentalization of nucleolar proteins that are suspected of phase separation. The nucleolus is the main hub of ribosome biogenesis and here we present data supporting the division of proteins into nucleolar domains based on their function in ribosome biogenesis. We also describe the use of vital dyes such as Hoechst 33342 and Thioflavin T in nucleolar staining. Additionally, we quantify nucleolar morphology changes induced by heat shock and actinomycin D treatments. We suggest these approaches will be valuable in a variety of studies that seek to better understand the nucleolus, particularly those regarding phase separation. These approaches may also be instructive for other studies on phase separation, especially in the nucleus. |
format | Online Article Text |
id | pubmed-9474603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94746032022-10-14 Component analysis of nucleolar protein compartments using Xenopus laevis oocytes Lavering, Emily D. Petros, Irini N. Weeks, Daniel L. Dev Growth Differ Versatile Utilities of Amphibians (Part 1) The nucleolus is a multi‐compartment, non‐membrane‐bound organelle within the nucleus. Nucleolar assembly is influenced by proteins capable of phase separation. Xenopus laevis oocytes contain hundreds of large nucleoli that provide experimental access for nucleoli that is unavailable in other systems. Here we detail methods to streamline the in vivo analysis of the compartmentalization of nucleolar proteins that are suspected of phase separation. The nucleolus is the main hub of ribosome biogenesis and here we present data supporting the division of proteins into nucleolar domains based on their function in ribosome biogenesis. We also describe the use of vital dyes such as Hoechst 33342 and Thioflavin T in nucleolar staining. Additionally, we quantify nucleolar morphology changes induced by heat shock and actinomycin D treatments. We suggest these approaches will be valuable in a variety of studies that seek to better understand the nucleolus, particularly those regarding phase separation. These approaches may also be instructive for other studies on phase separation, especially in the nucleus. John Wiley and Sons Inc. 2022-06-12 2022-08 /pmc/articles/PMC9474603/ /pubmed/35607824 http://dx.doi.org/10.1111/dgd.12794 Text en © 2022 The Authors. Development, Growth & Differentiation published by John Wiley & Sons Australia, Ltd on behalf of Japanese Society of Developmental Biologists. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Versatile Utilities of Amphibians (Part 1) Lavering, Emily D. Petros, Irini N. Weeks, Daniel L. Component analysis of nucleolar protein compartments using Xenopus laevis oocytes |
title | Component analysis of nucleolar protein compartments using Xenopus laevis oocytes |
title_full | Component analysis of nucleolar protein compartments using Xenopus laevis oocytes |
title_fullStr | Component analysis of nucleolar protein compartments using Xenopus laevis oocytes |
title_full_unstemmed | Component analysis of nucleolar protein compartments using Xenopus laevis oocytes |
title_short | Component analysis of nucleolar protein compartments using Xenopus laevis oocytes |
title_sort | component analysis of nucleolar protein compartments using xenopus laevis oocytes |
topic | Versatile Utilities of Amphibians (Part 1) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9474603/ https://www.ncbi.nlm.nih.gov/pubmed/35607824 http://dx.doi.org/10.1111/dgd.12794 |
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