دورية أكاديمية

Increasing Notch signaling antagonizes PRC2-mediated silencing to promote reprograming of germ cells into neurons

التفاصيل البيبلوغرافية
العنوان: Increasing Notch signaling antagonizes PRC2-mediated silencing to promote reprograming of germ cells into neurons
المؤلفون: Seelk, Stefanie, Adrian-Kalchhauser, Irene, Hargitai, Balázs, Hajduskova, Martina, Gutnik, Silvia, Tursun, Baris, Ciosk, Rafal
بيانات النشر: eLife Sciences Publications
سنة النشر: 2016
المجموعة: University of Basel: edoc
الوصف: Cell-fate reprograming is at the heart of development, yet very little is known about the molecular mechanisms promoting or inhibiting reprograming in intact organisms. In the C. elegans germline, reprograming germ cells into somatic cells requires chromatin perturbation. Here, we describe that such reprograming is facilitated by GLP-1/Notch signaling pathway. This is surprising, since this pathway is best known for maintaining undifferentiated germline stem cells/progenitors. Through a combination of genetics, tissue-specific transcriptome analysis, and functional studies of candidate genes, we uncovered a possible explanation for this unexpected role of GLP-1/Notch. We propose that GLP-1/Notch promotes reprograming by activating specific genes, silenced by the Polycomb repressive complex 2 (PRC2), and identify the conserved histone demethylase UTX-1 as a crucial GLP-1/Notch target facilitating reprograming. These findings have wide implications, ranging from development to diseases associated with abnormal Notch signaling.
نوع الوثيقة: article in journal/newspaper
اللغة: unknown
تدمد: 2050-084X
العلاقة: Seelk, Stefanie and Adrian-Kalchhauser, Irene and Hargitai, Balázs and Hajduskova, Martina and Gutnik, Silvia and Tursun, Baris and Ciosk, Rafal. (2016) Increasing Notch signaling antagonizes PRC2-mediated silencing to promote reprograming of germ cells into neurons. eLife, 5. pp. 1-22.; info:isi/000385524500001; info:pmid/27602485; urn:ISSN:2050-084X
DOI: 10.7554/eLife.15477
الإتاحة: https://doi.org/10.7554/eLife.15477Test
https://edoc.unibas.ch/59636Test/
حقوق: info:eu-repo/semantics/closedAccess
رقم الانضمام: edsbas.677ABF94
قاعدة البيانات: BASE
الوصف
تدمد:2050084X
DOI:10.7554/eLife.15477