lncRNA Panct1 Maintains Mouse Embryonic Stem Cell Identity by Regulating TOBF1 Recruitment to Oct-Sox Sequences in Early G1

Debojyoti Chakraborty, Maciej Paszkowski-Rogacz, Nicolas Berger, Li Ding, Jovan Mircetic, Jun Fu, Vytautas Iesmantavicius, Chunaram Choudhary, Konstantinos Anastassiadis, A Francis Stewart, Frank Buchholz

    15 Citations (Scopus)
    105 Downloads (Pure)

    Abstract

    Long noncoding RNAs (lncRNAs) have been implicated in diverse biological processes, including embryonic stem cell (ESC) maintenance. However, their functional mechanisms remain largely undefined. Here, we show that the lncRNA Panct1 regulates the transient recruitment of a putative X-chromosome-encoded protein A830080D01Rik, hereafter referred to as transient octamer binding factor 1 (TOBF1), to genomic sites resembling the canonical Oct-Sox motif. TOBF1 physically interacts with Panct1 and exhibits a cell-cycle-specific punctate localization in ESCs. At the chromatin level, this correlates with its recruitment to promoters of pluripotency genes. Strikingly, mutating an octamer-like motif in Panct1 RNA abrogates the strength of TOBF1 localization and recruitment to its targets. Taken together, our data reveal a tightly controlled spatial and temporal pattern of lncRNA-mediated gene regulation in a cell-cycle-dependent manner and suggest that lncRNAs might function as barcodes for identifying genomic addresses for maintaining cellular states. Chakraborty et al. molecularly characterize the lncRNA Panct1 in the maintenance of ESC identity. Their study reveals the tightly controlled, cell-cycle-dependent modulation of gene expression cooperatively mediated by Panct1 and the DNA-interacting protein TOBF1. Hence, lncRNAs might serve as barcodes for identifying genomic addresses that regulate cellular states.

    Original languageEnglish
    JournalCell Reports
    Volume21
    Issue number11
    Pages (from-to)3012-3021
    Number of pages10
    ISSN2211-1247
    DOIs
    Publication statusPublished - 12 Dec 2017

    Keywords

    • Journal Article

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