| Literature DB >> 34098113 |
Eric Fields1, Erik Vaughan1, Deepika Tripu1, Isabelle Lim1, Katherine Shrout1, Jessica Conway1, Nicole Salib1, Yubin Lee1, Akash Dhamsania1, Michael Jacobsen1, Ashley Woo1, Huijing Xue2, Kan Cao3.
Abstract
Huntington's disease (HD) is an autosomal neurodegenerative disorder caused by extended trinucleotide CAG repetition in the HTT gene. Wild-type huntingtin protein (HTT) is essential, involved in a variety of crucial cellular functions such as vesicle transportation, cell division, transcription regulation, autophagy, and tissue maintenance. The mutant HTT (mHTT) proteins in the body interfere with HTT's normal cellular functions and cause additional detrimental effects. In this review, we discuss multiple approaches targeting DNA and RNA to reduce mHTT expression. These approaches are categorized into non-allele-specific silencing and allele-specific-silencing using Single Nucleotide Polymorphisms (SNPs) and haplogroup analysis. Additionally, this review discusses a potential application of recent CRISPR prime editing technology in targeting HD.Entities:
Keywords: Allele-specific targeting; Huntington’s disease; Prime editing; SNPs
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Year: 2021 PMID: 34098113 PMCID: PMC8373677 DOI: 10.1016/j.arr.2021.101385
Source DB: PubMed Journal: Ageing Res Rev ISSN: 1568-1637 Impact factor: 11.788