RTEL1 (regulator of telomere length helicase 1) is a DNA helicase that has been identified more than 10 years ago. Many works since, mainly in the nematode Caenorhabditis elegans and the mouse, have highlighted its role in chromosomal stability, maintenance of telomere length, and DNA repair. Recently, four laboratories have characterized RTEL1 mutations in patients with dyskeratosis congenita (DC) and Hoyeraal-Hreidarsson (HH) syndrome, a rare and severe variant of DC. We here summarize the current knowledge on RTEL1 and discuss the possible other functions that RTEL1 could play. © 2013 médecine/ sciences-Inserm.
CITATION STYLE
Le Guen, T., Jullien, L., Schertzer, M., Lefebvre, A., Kermasson, L., De Villartay, J. P., … Revy, P. (2013). RTEL1, une hélicase de l’ADN essentielle à la stabilité du génome. Medecine/Sciences. Editions EDK. https://doi.org/10.1051/medsci/20132912018
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