Repression-free utrophin-A 5'UTR variants.

Mol Biol Res Commun

Department of Molecular Biology and Biotechnology, University of Kalyani, Kalyani, Nadia, 741235 India.

Published: September 2019

Mutation in the dystrophin gene results Duchenne Muscular Dystrophy (DMD), an X-linked fatal neuromuscular disorder. Dystrophin deficiency can be compensated by upregulation of utrophin, an autosomal homologue of dystrophin. But the expression of utrophin in adults is restricted to myotendinous and neuromuscular junctions. Therefore utrophin upregulation throughout the muscle fiber can only be achieved if we understand regulatory mechanisms behind its expression. Utrophin-A 5'UTR mediated repression of translation was reported earlier. In this article, we present evidences of two transcript variants of utrophin-A that do not confer repression to the downstream reporter ORF in mouse myoblast C2C12 cells. These repression-free variants may be targeted for utrophin upregulation.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6802688PMC
http://dx.doi.org/10.22099/mbrc.2019.34240.1421DOI Listing

Publication Analysis

Top Keywords

utrophin-a 5'utr
8
utrophin upregulation
8
repression-free utrophin-a
4
5'utr variants
4
variants mutation
4
mutation dystrophin
4
dystrophin gene
4
gene duchenne
4
duchenne muscular
4
muscular dystrophy
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!