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Genome organization regulates nuclear pore complex formation and promotes differentiation during Drosophila oogenesis
Genome organization can regulate gene expression and promote cell fate transitions. The differentiation of germline stem cells (GSCs) to oocytes in Drosophila involves changes in genome organization mediated by heterochromatin and the nuclear pore complex (NPC). Heterochromatin represses germ-cell g...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10680722/ https://www.ncbi.nlm.nih.gov/pubmed/38014330 http://dx.doi.org/10.1101/2023.11.15.567233 |
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author | Kotb, Noor M. Ulukaya, Gulay Chavan, Ankita Nguyen, Son C. Proskauer, Lydia Joyce, Eric Hasson, Dan Jagannathan, Madhav Rangan, Prashanth |
author_facet | Kotb, Noor M. Ulukaya, Gulay Chavan, Ankita Nguyen, Son C. Proskauer, Lydia Joyce, Eric Hasson, Dan Jagannathan, Madhav Rangan, Prashanth |
author_sort | Kotb, Noor M. |
collection | PubMed |
description | Genome organization can regulate gene expression and promote cell fate transitions. The differentiation of germline stem cells (GSCs) to oocytes in Drosophila involves changes in genome organization mediated by heterochromatin and the nuclear pore complex (NPC). Heterochromatin represses germ-cell genes during differentiation and NPCs anchor these silenced genes to the nuclear periphery, maintaining silencing to allow for oocyte development. Surprisingly, we find that genome organization also contributes to NPC formation, mediated by the transcription factor Stonewall (Stwl). As GSCs differentiate, Stwl accumulates at boundaries between silenced and active gene compartments. Stwl at these boundaries plays a pivotal role in transitioning germ-cell genes into a silenced state and activating a group of oocyte genes and Nucleoporins (Nups). The upregulation of these Nups during differentiation is crucial for NPC formation and further genome organization. Thus, crosstalk between genome architecture and NPCs is essential for successful cell fate transitions. |
format | Online Article Text |
id | pubmed-10680722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-106807222023-11-27 Genome organization regulates nuclear pore complex formation and promotes differentiation during Drosophila oogenesis Kotb, Noor M. Ulukaya, Gulay Chavan, Ankita Nguyen, Son C. Proskauer, Lydia Joyce, Eric Hasson, Dan Jagannathan, Madhav Rangan, Prashanth bioRxiv Article Genome organization can regulate gene expression and promote cell fate transitions. The differentiation of germline stem cells (GSCs) to oocytes in Drosophila involves changes in genome organization mediated by heterochromatin and the nuclear pore complex (NPC). Heterochromatin represses germ-cell genes during differentiation and NPCs anchor these silenced genes to the nuclear periphery, maintaining silencing to allow for oocyte development. Surprisingly, we find that genome organization also contributes to NPC formation, mediated by the transcription factor Stonewall (Stwl). As GSCs differentiate, Stwl accumulates at boundaries between silenced and active gene compartments. Stwl at these boundaries plays a pivotal role in transitioning germ-cell genes into a silenced state and activating a group of oocyte genes and Nucleoporins (Nups). The upregulation of these Nups during differentiation is crucial for NPC formation and further genome organization. Thus, crosstalk between genome architecture and NPCs is essential for successful cell fate transitions. Cold Spring Harbor Laboratory 2023-11-16 /pmc/articles/PMC10680722/ /pubmed/38014330 http://dx.doi.org/10.1101/2023.11.15.567233 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Kotb, Noor M. Ulukaya, Gulay Chavan, Ankita Nguyen, Son C. Proskauer, Lydia Joyce, Eric Hasson, Dan Jagannathan, Madhav Rangan, Prashanth Genome organization regulates nuclear pore complex formation and promotes differentiation during Drosophila oogenesis |
title | Genome organization regulates nuclear pore complex formation and promotes differentiation during Drosophila oogenesis |
title_full | Genome organization regulates nuclear pore complex formation and promotes differentiation during Drosophila oogenesis |
title_fullStr | Genome organization regulates nuclear pore complex formation and promotes differentiation during Drosophila oogenesis |
title_full_unstemmed | Genome organization regulates nuclear pore complex formation and promotes differentiation during Drosophila oogenesis |
title_short | Genome organization regulates nuclear pore complex formation and promotes differentiation during Drosophila oogenesis |
title_sort | genome organization regulates nuclear pore complex formation and promotes differentiation during drosophila oogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10680722/ https://www.ncbi.nlm.nih.gov/pubmed/38014330 http://dx.doi.org/10.1101/2023.11.15.567233 |
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