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A nuclear architecture screen in Drosophila identifies Stonewall as a link between chromatin position at the nuclear periphery and germline stem cell fate

The association of genomic loci to the nuclear periphery is proposed to facilitate cell-type specific gene repression and influence cell fate decisions. However, the interplay between gene position and expression remains incompletely understood, in part because the proteins that position genomic loc...

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Autores principales: Chavan, Ankita, Isenhart, Randi, Nguyen, Son C., Kotb, Noor, Harke, Jailynn, Sintsova, Anna, Ulukaya, Gulay, Uliana, Federico, Ashiono, Caroline, Kutay, Ulrike, Pegoraro, Gianluca, Rangan, Prashanth, Joyce, Eric F., Jagannathan, Madhav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10680830/
https://www.ncbi.nlm.nih.gov/pubmed/38014085
http://dx.doi.org/10.1101/2023.11.17.567611
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author Chavan, Ankita
Isenhart, Randi
Nguyen, Son C.
Kotb, Noor
Harke, Jailynn
Sintsova, Anna
Ulukaya, Gulay
Uliana, Federico
Ashiono, Caroline
Kutay, Ulrike
Pegoraro, Gianluca
Rangan, Prashanth
Joyce, Eric F.
Jagannathan, Madhav
author_facet Chavan, Ankita
Isenhart, Randi
Nguyen, Son C.
Kotb, Noor
Harke, Jailynn
Sintsova, Anna
Ulukaya, Gulay
Uliana, Federico
Ashiono, Caroline
Kutay, Ulrike
Pegoraro, Gianluca
Rangan, Prashanth
Joyce, Eric F.
Jagannathan, Madhav
author_sort Chavan, Ankita
collection PubMed
description The association of genomic loci to the nuclear periphery is proposed to facilitate cell-type specific gene repression and influence cell fate decisions. However, the interplay between gene position and expression remains incompletely understood, in part because the proteins that position genomic loci at the nuclear periphery remain unidentified. Here, we used an Oligopaint-based HiDRO screen targeting ~1000 genes to discover novel regulators of nuclear architecture in Drosophila cells. We identified the heterochromatin-associated protein, Stonewall (Stwl), as a factor promoting perinuclear chromatin positioning. In female germline stem cells (GSCs), Stwl binds and positions chromatin loci, including GSC differentiation genes, at the nuclear periphery. Strikingly, Stwl-dependent perinuclear positioning is associated with transcriptional repression, highlighting a likely mechanism for Stwl’s known role in GSC maintenance and ovary homeostasis. Thus, our study identifies perinuclear anchors in Drosophila and demonstrates the importance of gene repression at the nuclear periphery for cell fate.
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spelling pubmed-106808302023-11-27 A nuclear architecture screen in Drosophila identifies Stonewall as a link between chromatin position at the nuclear periphery and germline stem cell fate Chavan, Ankita Isenhart, Randi Nguyen, Son C. Kotb, Noor Harke, Jailynn Sintsova, Anna Ulukaya, Gulay Uliana, Federico Ashiono, Caroline Kutay, Ulrike Pegoraro, Gianluca Rangan, Prashanth Joyce, Eric F. Jagannathan, Madhav bioRxiv Article The association of genomic loci to the nuclear periphery is proposed to facilitate cell-type specific gene repression and influence cell fate decisions. However, the interplay between gene position and expression remains incompletely understood, in part because the proteins that position genomic loci at the nuclear periphery remain unidentified. Here, we used an Oligopaint-based HiDRO screen targeting ~1000 genes to discover novel regulators of nuclear architecture in Drosophila cells. We identified the heterochromatin-associated protein, Stonewall (Stwl), as a factor promoting perinuclear chromatin positioning. In female germline stem cells (GSCs), Stwl binds and positions chromatin loci, including GSC differentiation genes, at the nuclear periphery. Strikingly, Stwl-dependent perinuclear positioning is associated with transcriptional repression, highlighting a likely mechanism for Stwl’s known role in GSC maintenance and ovary homeostasis. Thus, our study identifies perinuclear anchors in Drosophila and demonstrates the importance of gene repression at the nuclear periphery for cell fate. Cold Spring Harbor Laboratory 2023-11-17 /pmc/articles/PMC10680830/ /pubmed/38014085 http://dx.doi.org/10.1101/2023.11.17.567611 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Chavan, Ankita
Isenhart, Randi
Nguyen, Son C.
Kotb, Noor
Harke, Jailynn
Sintsova, Anna
Ulukaya, Gulay
Uliana, Federico
Ashiono, Caroline
Kutay, Ulrike
Pegoraro, Gianluca
Rangan, Prashanth
Joyce, Eric F.
Jagannathan, Madhav
A nuclear architecture screen in Drosophila identifies Stonewall as a link between chromatin position at the nuclear periphery and germline stem cell fate
title A nuclear architecture screen in Drosophila identifies Stonewall as a link between chromatin position at the nuclear periphery and germline stem cell fate
title_full A nuclear architecture screen in Drosophila identifies Stonewall as a link between chromatin position at the nuclear periphery and germline stem cell fate
title_fullStr A nuclear architecture screen in Drosophila identifies Stonewall as a link between chromatin position at the nuclear periphery and germline stem cell fate
title_full_unstemmed A nuclear architecture screen in Drosophila identifies Stonewall as a link between chromatin position at the nuclear periphery and germline stem cell fate
title_short A nuclear architecture screen in Drosophila identifies Stonewall as a link between chromatin position at the nuclear periphery and germline stem cell fate
title_sort nuclear architecture screen in drosophila identifies stonewall as a link between chromatin position at the nuclear periphery and germline stem cell fate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10680830/
https://www.ncbi.nlm.nih.gov/pubmed/38014085
http://dx.doi.org/10.1101/2023.11.17.567611
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