In vitro mechanism for the repair of muscle differentiation in DM1

WPRE element induces nuclear export of Myotonic Dystrophy transcripts and mediate the repair of muscle differentiation

79,00 €
(inkl. MwSt.)
In den Warenkorb

Lieferbar innerhalb 1 - 2 Wochen

Bibliografische Daten
ISBN/EAN: 9783659275524
Sprache: Englisch
Umfang: 200 S.
Format (T/L/B): 1.2 x 22 x 15 cm
Auflage: 1. Auflage 2012
Einband: kartoniertes Buch

Beschreibung

The woodchuck post-transcriptional regulatory element (WPRE) can naturally accumulate hepatitis transcripts in the cytoplasm, and has been recently exploited as an enhancer of transgene expression. The retention of mutant myotonic dystrophy protein kinase (DMPK) transcripts in the nucleus of myotonic dystrophy (DM) cells has an important pathogenic role in the disease, resulting in pleiotropic effects including delayed myoblast differentiation. In this study, we report the first use of WPRE as a tool to enhance nuclear export of an aberrantly retained messenger RNA. Stable cell lines expressing the normal and mutant DMPK 3' UTR (3' untranslated region) complementary DNA, with or without WPRE, were produced. It is noteworthy that WPRE stimulated extensive transport of mutant transcripts to the cytoplasm. This was associated with repair of the defective cellular MyoD levels and a subsequent increase in myoblast differentiation. These results provide the basis for a cellular model that can be exploited in DM and in the study of RNA transport mechanisms.

Autorenportrait

Dr. Mastroyiannopoulos received his BSc degree in Biomedical Sciences and his PhD degree from the University of Bristol. As from 2006, Dr. Mastroyiannopoulos has been appointed as a post-doctoral fellow at the Cyprus Institute of Neurology and Genetics and a Lecturer at the Cyprus School of Molecular Medicine.