NFIB influences progenitor competence in maturation of GABAergic neurons in mice

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Publicat a:bioRxiv (Jan 8, 2025)
Autor principal: Ann Rose Bright
Altres autors: Kotlyarenko, Yana, Neuhaus, Florian, Rodrigues, Diana, Chao, Feng, Peters, Christian, Vitali, Ilaria, Doenmez, Elif, Myoga, Michael H, Dvoretskova, Elena, Mayer, Christian
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Cold Spring Harbor Laboratory Press
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Accés en línia:Citation/Abstract
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LEADER 00000nab a2200000uu 4500
001 3152785505
003 UK-CbPIL
022 |a 2692-8205 
024 7 |a 10.1101/2024.03.18.585524  |2 doi 
035 |a 3152785505 
045 0 |b d20250108 
100 1 |a Ann Rose Bright 
245 1 |a NFIB influences progenitor competence in maturation of GABAergic neurons in mice 
260 |b Cold Spring Harbor Laboratory Press  |c Jan 8, 2025 
513 |a Working Paper 
520 3 |a Diverse types of GABAergic projection neurons and interneurons of the telencephalon derive from progenitors in a ventral germinal zone, called the ganglionic eminence. Using single-cell transcriptomics, chromatin accessibility profiling, lineage tracing, birthdating, heterochronic transplantation, and perturbation sequencing in mouse embryos, we investigated how progenitor competence influences the maturation and differentiation of these neurons. We found that the progression of neurogenesis over developmental time shapes maturation competence in ganglionic eminence progenitors, how they progress into mature states. In contrast, dierentiation competence, which defines the ability to produce diverse transcriptomic identities, remains largely unaffected by the stages of neurogenesis. Chromatin remodeling alongside a NFIB-driven regulatory gene module influences maturation competence in late-born neurons. These findings provide key insights into how transcriptional programs and chromatin accessibility govern neuronal maturation and the diversification of GABAergic neuron subtypes during neurodevelopment.Competing Interest StatementThe authors have declared no competing interest.Footnotes* The new version of the manuscript contains additional experiments, including CUT&RUN, in vivo overexpression, and tCROP-seq perturbation sequencing, providing functional validation and further supporting our conclusions on the role of NFIB in neuronal progenitor regulation.* http://141.5.108.55:3838/mind_shiny/ 
610 4 |a National Federation of Independent Business 
653 |a Neural stem cells 
653 |a Embryos 
653 |a Neurons 
653 |a Neurogenesis 
653 |a Maturation 
653 |a Interneurons 
653 |a γ-Aminobutyric acid 
653 |a Telencephalon 
653 |a Chromatin remodeling 
653 |a Transcriptomics 
653 |a Progenitor cells 
653 |a Developmental stages 
700 1 |a Kotlyarenko, Yana 
700 1 |a Neuhaus, Florian 
700 1 |a Rodrigues, Diana 
700 1 |a Chao, Feng 
700 1 |a Peters, Christian 
700 1 |a Vitali, Ilaria 
700 1 |a Doenmez, Elif 
700 1 |a Myoga, Michael H 
700 1 |a Dvoretskova, Elena 
700 1 |a Mayer, Christian 
773 0 |t bioRxiv  |g (Jan 8, 2025) 
786 0 |d ProQuest  |t Biological Science Database 
856 4 1 |3 Citation/Abstract  |u https://www.proquest.com/docview/3152785505/abstract/embedded/6A8EOT78XXH2IG52?source=fedsrch 
856 4 0 |3 Full text outside of ProQuest  |u https://www.biorxiv.org/content/10.1101/2024.03.18.585524v2