RTEL1 influences the abundance and localization of TERRA RNA Journal Article


Authors: Ghisays, F.; Garzia, A.; Wang, H.; Canasto-Chibuque, C.; Hohl, M.; Savage, S. A.; Tuschl, T.; Petrini, J. H. J.
Article Title: RTEL1 influences the abundance and localization of TERRA RNA
Abstract: Telomere repeat containing RNAs (TERRAs) are a family of long non-coding RNAs transcribed from the subtelomeric regions of eukaryotic chromosomes. TERRA transcripts can form R-loops at chromosome ends; however the importance of these structures or the regulation of TERRA expression and retention in telomeric R-loops remain unclear. Here, we show that the RTEL1 (Regulator of Telomere Length 1) helicase influences the abundance and localization of TERRA in human cells. Depletion of RTEL1 leads to increased levels of TERRA RNA while reducing TERRA-containing R loops at telomeres. In vitro, RTEL1 shows a strong preference for binding G-quadruplex structures which form in TERRA. This binding is mediated by the C-terminal region of RTEL1, and is independent of the RTEL1 helicase domain. RTEL1 binding to TERRA appears to be essential for cell viability, underscoring the importance of this function. Degradation of TERRA-containing R-loops by overexpression of RNAse H1 partially recapitulates the increased TERRA levels and telomeric instability associated with RTEL1 deficiency. Collectively, these data suggest that regulation of TERRA is a key function of the RTEL1 helicase, and that loss of that function may contribute to the disease phenotypes of patients with RTEL1 mutations. © 2021, The Author(s).
Keywords: dna binding protein; genetics; mutation; dna-binding proteins; protein domain; chromosome; telomere; metabolism; gene expression; transcription factor; transcription factors; rna; chemistry; sequence alignment; eukaryota; dna helicases; dna helicase; protein domains; ribonuclease h; hek293 cells; gene knockout techniques; humans; human; hek293 cell line; gene knockout; dmrt2 protein, human; ribonuclease hi; rtel1 protein, human; r-loop structures
Journal Title: Nature Communications
Volume: 12
ISSN: 2041-1723
Publisher: Nature Publishing Group  
Date Published: 2021-05-21
Start Page: 3016
Language: English
DOI: 10.1038/s41467-021-23299-2
PUBMED: 34021146
PROVIDER: scopus
PMCID: PMC8140157
DOI/URL:
Notes: Article -- Export Date: 1 July 2021 -- Source: Scopus
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  1. John Petrini
    94 Petrini
  2. Marcel Hohl
    13 Hohl
  3. Hexiao Wang
    2 Wang