Document Type
Article
Journal Title
Journal of biosciences
Publication Date
Winter 2-1-2002
Volume
27
Abstract
Fourteen genetic neurodegenerative diseases and three fragile sites have been associated with the expansion of (CTG)n (CAG)n, (CGG)n (CCG)n, or (GAA)n (TTC)n repeat tracts. Different models have been proposed for the expansion of triplet repeats, most of which presume the formation of alternative DNA structures in repeat tracts. One of the most likely structures, slipped strand DNA, may stably and reproducibly form within triplet repeat sequences. The propensity to form slipped strand DNA is proportional to the length and homogeneity of the repeat tract. The remarkable stability of slipped strand DNA may, in part, be due to loop-loop interactions facilitated by the sequence complementarity of the loops and the dynamic structure of three-way junctions formed at the loop-outs.
MeSH Headings
DNA, Humans, Microscopy, Atomic Force, Models, Genetic, Mutation, Neurodegenerative Diseases, Nucleic Acid Conformation, Trinucleotide Repeat Expansion, Trinucleotide Repeats
DOI Link
ISSN
0250-5991
Rights
The Indian Academy of Sciences owns the copyright in all articles and Academy-provided commentary contained in the journal.
Recommended Citation
Sinden, Richard R.; Potaman, Vladimir N.; Oussatcheva, Elena A.; Pearson, Christopher E.; Lyubchenko, Yuri L.; and Shlyakhtenko, Luda S., "Triplet repeat DNA structures and human genetic disease: dynamic mutations from dynamic DNA." (2002). Journal Articles: Pharmaceutical Sciences. 11.
https://digitalcommons.unmc.edu/cop_pharmsci_articles/11