Genome organization regulates nuclear pore complex formation and promotes differentiation duringDrosophilaoogenesis
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Published:2024-06-12
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ISSN:0890-9369
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Container-title:Genes & Development
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language:en
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Short-container-title:Genes Dev.
Author:
Kotb Noor M.,
Ulukaya Gulay,
Chavan Ankita,
Nguyen Son C.,
Proskauer Lydia,
Joyce Eric F.,
Hasson Dan,
Jagannathan MadhavORCID,
Rangan Prashanth
Abstract
Genome organization can regulate gene expression and promote cell fate transitions. The differentiation of germline stem cells (GSCs) to oocytes inDrosophilainvolves 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 found 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, cross-talk between genome architecture and NPCs is essential for successful cell fate transitions.
Funder
NIH/NIGMS
Clinical and Translational Science Awards
National Center for Advancing Translational Sciences
Office of Research Infrastructure of the
National Institutes of Health
Publisher
Cold Spring Harbor Laboratory