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Discovery of Triplet Stabilizing Factor Fans Hope for Huntington’s and Other...

New research has identified a mechanism in the DNA mismatch repair pathway that stops the abnormal trinucleotide repeat expansion and the progression of Huntington’s disease. Scientists at the University College of London (UCL) and the University of Cambridge show FAN1, a genetic modifier of Huntington’s disease stabilizes CAG repeats by binding MLH1 to restrict its binding to MSH3, thus inhibiting the assembly of a functional mismatch repair complex. This pivotal role of FAN1 highlights a potential avenue for HD therapeutics since mimicking or enhancing FAN1 mediated blocking of mismatch repair would alter the course of the disease.

Triplet’s New Huntington Disease Drug May Also Treat Other Repeat Expansion...

Triplet Therapeutics presented preclinical data on their new antisense oligonucleotide drug for Huntington’s Disease at the CHDI Foundation’s 16th Annual HD Therapeutics Conference. The drug that targets MSH3 in the DDR pathway may also be applicable for other repeat expansion disorders. Highlighting its long-term commitment to patients, the company pledged 1% equity in a trust fund for patients.