Présentation des projets sur le site web

Chaque projet soutenu par Gebert Rüf Stiftung est présenté sur le site web de la fondation avec en particulier les données de base du projet. Par cette publication, la fondation informe sur les résultats du soutien accordé et contribue à la communication scientifique au sein de la société.


Treating Myotonic Dystrophy – Rare Diseases 2014


Für den Inhalt der Angaben zeichnet die Projektleitung verantwortlich.


This project is co-funded by UNISCIENTIA STIFTUNG and is one of the five winners of the call 2014 «Rare Diseases - New Approaches» Project partners: University of Basel

Données de projet

  • Numéro du projet: GRS-060/14 
  • Subside accordé: CHF 420'000 
  • Consentement: 06.11.2014 
  • Durée: 02.2015 - 10.2018 
  • Champs d'activité:  Rare Diseases, 2009 - 2014

Direction du projet

Description du projet

There is currently no cure for myotonic dystrophy type 1 (DM1). The disease affects about 1 in 8000 individuals world-wide and patients develop problems with muscle relaxation (myotonia), muscle weakness and wasting, as well as cardiac abnormalities. Patients also develop cataracts and diabetes in addition to experiencing decreased motivation and daytime sleepiness.

DM1 is results from the expansion of a trinucleotide repeat in an unstranslated region of the mRNA coding for the myotonic dystrophy protein kinase (DMPK). Importantly, the longer the repeat tract, the more severe the symptoms are. It has therefore been proposed that reducing – referred to as contracting – the repeat tract down to a normal length would effectively remove the underlying cause of the disease and provide a therapeutic avenue. The goal of this project is to test this idea and provide the proof-of-concept that this is a viable option to treat patients.

Quelles sont les particularités de ce projet?

Most treatments currently being developed, predominantly based on pharmaceutical molecules, aim to reduce the symptoms of the disease and are meant to be administered throughout a patient’s life, which brings up issues of long term toxicity. An alternative could include treatments designed to tackle the cause rather than the symptoms of DM1.

The correlation between repeat length and the severity of the symptoms was noticed over 20 years ago, yet repeat contraction has never been tested for its potential beneficial effects. This is mainly due to the lack of approaches that can specifically induce contractions. This is a limitation because if expansions are also caused by the treatment, then the disease symptoms would worsen. Here are testing a new customizable system, CRISPR-Cas9, for the ability to induce contractions.

DM1 is part of a family of neurodegenerative, neuromuscular, and neurological diseases caused by the expansion of trinucleotide repeats. While these diseases are phenotypically distinct, they all share a common cause: the expanded repeat. We therefore anticipate the approach tested here for DM1 will also be applicable to a wide variety of devastating diseases.

Etat/résultats intermédiaires

We now have shown that using a variant of the CRISPR-Cas9 enzyme (Cas9 D10A) that makes nicks on the DNA rather than cutting both strands, we can specifically induce contractions in human cell lines. This effect is specific for the expanded allele, leaving the essential normal allele that patients also carry intact. Furthermore, we were unable to detect off-target mutations using this approach, which could target all 14 different diseases caused by the expansion of CAG/CTG repeats. We are now turning our attention to the question of whether repeat contraction can reverse the cellular phenotypes in patient-derived cells and in murine models for multiple expanded repeat diseases.


Cinzia Cinesi, Lorène Aeschbach, Bin Yang, and Vincent Dion. Contracting CAG/CTG repeats using the CRISPR-Cas9 nickase. Nat. Commun. 7, 13272 doi: 10.1038/ncomms13272 (2016).

Personnes participant au projet

Dernière mise à jour de cette présentation du projet  26.11.2020