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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...

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Autores principales: Kotb, Noor M., Ulukaya, Gulay, Chavan, Ankita, Nguyen, Son C., Proskauer, Lydia, Joyce, Eric, Hasson, Dan, Jagannathan, Madhav, Rangan, Prashanth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
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.
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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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