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基因 · Muscle

DMD

Dystrophin — The largest gene in the human genome, encoding dystrophin — the shock absorber that keeps muscle fibres intact as they contract.

Xp21.2-p21.1 musclelargest gene
染色体 X DMD Xp21.2-p21.1 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

DMD is the biggest gene humans have, spanning over two million letters of DNA. It makes dystrophin, a long springy protein that anchors the inside of a muscle cell to its outer membrane. Without it, every contraction tears the cell a little, and muscle is gradually lost. Its enormous size is a large part of why treating it is so hard: it will not fit into standard delivery vehicles.

DMD, at Xp21.2-p21.1, spans approximately 2.2 million base pairs with 79 exons and encodes dystrophin, which links the actin cytoskeleton to the extracellular matrix through the dystrophin-glycoprotein complex. Out-of-frame mutations abolish the protein and cause Duchenne muscular dystrophy; in-frame deletions produce a truncated but partly functional protein and the milder Becker phenotype — the observation that underlies exon-skipping strategies.

Sources

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

Connected in the Atlas

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