Literature DB >> 32773039

Differentiating Drosophila female germ cells initiate Polycomb silencing by regulating PRC2-interacting proteins.

Steven Z DeLuca1, Megha Ghildiyal1, Liang-Yu Pang1, Allan C Spradling1.   

Abstract

Polycomb silencing represses gene expression and provides a molecular memory of chromatin state that is essential for animal development. We show that Drosophila female germline stem cells (GSCs) provide a powerful system for studying Polycomb silencing. GSCs have a non-canonical distribution of PRC2 activity and lack silenced chromatin like embryonic progenitors. As GSC daughters differentiate into nurse cells and oocytes, nurse cells, like embryonic somatic cells, silence genes in traditional Polycomb domains and in generally inactive chromatin. Developmentally controlled expression of two Polycomb repressive complex 2 (PRC2)-interacting proteins, Pcl and Scm, initiate silencing during differentiation. In GSCs, abundant Pcl inhibits PRC2-dependent silencing globally, while in nurse cells Pcl declines and newly induced Scm concentrates PRC2 activity on traditional Polycomb domains. Our results suggest that PRC2-dependent silencing is developmentally regulated by accessory proteins that either increase the concentration of PRC2 at target sites or inhibit the rate that PRC2 samples chromatin.
© 2020, DeLuca et al.

Entities:  

Keywords:  D. melanogaster; PRC2; chromatin; chromosomes; differentiation; epigenetic; gene expression; nurse cell; polycomb

Mesh:

Substances:

Year:  2020        PMID: 32773039      PMCID: PMC7438113          DOI: 10.7554/eLife.56922

Source DB:  PubMed          Journal:  Elife        ISSN: 2050-084X            Impact factor:   8.140


  130 in total

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6.  Differentiating Drosophila female germ cells initiate Polycomb silencing by regulating PRC2-interacting proteins.

Authors:  Steven Z DeLuca; Megha Ghildiyal; Liang-Yu Pang; Allan C Spradling
Journal:  Elife       Date:  2020-08-10       Impact factor: 8.140

7.  Three classes of epigenomic regulators converge to hyperactivate the essential maternal gene deadhead within a heterochromatin mini-domain.

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  7 in total

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