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- W1976913448 abstract "Polycomb group (PcG) proteins are key chromatin regulators implicated in multiple processes including embryonic development, tissue homeostasis, genomic imprinting, X-chromosome inactivation, and germ cell differentiation. The PcG proteins recognize target genomic loci through cis DNA sequences known as Polycomb Response Elements (PREs), which are well characterized in Drosophila. However, mammalian PREs have been elusive until two groups reported putative mammalian PREs recently. Consistent with the existence of mammalian PREs, here we report the identification and characterization of a potential PRE from human T cells. The putative human PRE has enriched binding of PcG proteins, and such binding is dependent on a key PcG component SUZ12. We demonstrate that the putative human PRE carries both genetic and molecular features of Drosophila PRE in transgenic flies, implying that not only the trans PcG proteins but also certain features of the cis PREs are conserved between mammals and Drosophila." @default.
- W1976913448 created "2016-06-24" @default.
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- W1976913448 date "2012-05-03" @default.
- W1976913448 modified "2023-10-14" @default.
- W1976913448 title "A Novel Human Polycomb Binding Site Acts As a Functional Polycomb Response Element in Drosophila" @default.
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- W1976913448 doi "https://doi.org/10.1371/journal.pone.0036365" @default.
- W1976913448 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3343078" @default.
- W1976913448 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/22570707" @default.
- W1976913448 hasPublicationYear "2012" @default.
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