The definitive guide to gene editing.
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Gene · Neurological

HTT

Huntingtin — Encodes huntingtin; an expanded CAG repeat in it causes Huntington's disease through a toxic gain of function.

4p16.3 brainrepeat expansion
Chromosome 4 HTT 4p16.3 p q

Schematic only — arm proportions are approximate and band detail is not drawn to scale. Cytogenetic location as published by NCBI Gene.

What this gene does

Near the start of the HTT gene is a short sequence — CAG — repeated over and over. Most people have fewer than 27 repeats. If the number grows past about 40, the protein made from the gene acquires a harmful new property and slowly kills brain cells. The more repeats, the earlier symptoms tend to begin.

HTT, at 4p16.3, encodes huntingtin, a large scaffolding protein with roles in vesicle transport and development. Expansion of the exon 1 CAG tract above roughly 40 repeats produces a polyglutamine tract conferring toxic gain of function, with an inverse relationship between repeat length and age of onset. Because wild-type huntingtin is essential, allele-selective strategies are preferred over total lowering.

Sources

  • MedlinePlus Genetics, U.S. National Library of Medicine
    HTT gene ↗

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