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基因 · Metabolic

TTR

Transthyretin — Encodes a liver protein that carries thyroid hormone and vitamin A — and which, when it misfolds, forms the deposits of ATTR amyloidosis.

18q12.1 liveramyloidin vivo
染色体 18 TTR 18q12.1 p q

仅为示意图——染色体臂比例为近似值,条带细节未按比例绘制。细胞遗传学位置以 NCBI Gene 公布的数据为准。

这个基因的功能

The liver makes transthyretin as a transport protein, moving thyroid hormone and vitamin A around the body. It normally travels as a group of four joined together. If that group comes apart, the individual pieces misfold and clump into deposits that damage nerves and heart muscle. Because people who make very little transthyretin seem to do fine, switching the gene off is a reasonable treatment strategy.

TTR, at 18q12.1, encodes transthyretin, a homotetrameric transport protein for thyroxine and retinol-binding protein. Destabilising variants — over 130 are known, V30M and V122I among the most common — promote tetramer dissociation and amyloid fibril formation. Since circulating transthyretin is almost entirely hepatic and low levels appear well tolerated, hepatic knockout is a rational one-time strategy, pursued by in vivo CRISPR alongside approved stabilisers and RNA silencers.

Sources

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

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