Alternative splicing, a molecular process that’s crucial for genes being “read” to produce proteins, is dysregulated in Huntington’s disease from the early stages of neuronal development, as indicated in a recent study published in eBioMedicine. Notably, splicing changes were found to be dependent on the length of CAG repeats in the HTT gene — the cause of Huntington’s.
“We identified several molecular processes that are enriched in [alterative splicing] events and may represent feedback loops of RNA processing dysregulation,” according to scientists behind the report. Click here to learn more.
|