Skip to main content
Cellular and Molecular Life Sciences: CMLS logoLink to Cellular and Molecular Life Sciences: CMLS
. 2000 Jun;57(6):914–931. doi: 10.1007/PL00000734

DNA repeat expansions and human disease

K Usdin* 1, E Grabczyk 1
PMCID: PMC11146815  PMID: 10950307

Abstract.

The repeat expansion diseases are genetic disorders caused by intergenerational expansions of a specific tandem DNA repeat. These disorders range from mildly to severely debilitating or fatal, and all have limited treatment options. How expansion occurs and causes disease is only now beginning to be understood. Efforts to model expansion in mice have so far met with only limited success, perhaps due to a requirement for specific cis- or trans-acting factors. In vitro studies and data from bacteria and yeast suggest that in addition to secondary structures formed by the repeats, components of the DNA replication and recombination machinery are important determinants of instability. The consequences of expansion differ depending on where in the gene the repeat tract is located, and range from reduction of transcription initiation to protein toxicity. Recent advances are beginning to make rational approaches to the development of therapies possible.

Keywords: Key words. Repeat expansion; DNA instability; DNA structure; triplet repeats; polyglutamine toxicity.

Footnotes

Received 13 December 1999; received after revision 3 February 2000; accepted 7 February 2000

Change history

8/31/2024

An Erratum to this paper has been published: 10.1007/PL00000648


Articles from Cellular and Molecular Life Sciences: CMLS are provided here courtesy of Springer

RESOURCES