UCL Institute of Neurology, Queen Square, London WC1N, UK.
IRCCS San Raffaele Scientific Institute, DIBIT, Milan, Italy.
Hum Mol Genet. 2019 Jan 1;28(1):124-132. doi: 10.1093/hmg/ddy336.
Protein zero (P0) is the major structural protein in peripheral myelin, and mutations in the Myelin Protein Zero (Mpz) gene produce wide-ranging hereditary neuropathy phenotypes. To gain insight in the mechanisms underlying a particularly severe form, congenital hypomyelination (CH), we targeted mouse Mpz to encode P0Q215X, a nonsense mutation associated with the disease, that we show escapes nonsense mediated decay and is expressed in CH patient nerves. The knock-in mice express low levels of the resulting truncated protein, producing a milder phenotype when compared to patients, allowing to dissect the subtle pathogenic mechanisms occurring in otherwise very compromised peripheral myelin. We find that P0Q215X does not elicit an unfolded protein response, which is a key mechanism for other pathogenic MPZ mutations, but is instead in part aberrantly trafficked to non-myelin plasma membranes and induces defects in radial sorting of axons by Schwann cells. We show that the loss of the C-terminal Tyr-Ala-Met-Leu motif is responsible for P0 mislocalization, as its addition is able to restore correct P0Q215X trafficking in vitro. Lastly, we show that P0Q215X acts through dose-dependent gain of abnormal function, as wild-type P0 is unable to rescue the hypomyelination phenotype. Collectively, these data indicate that alterations at the premyelinating stage, linked to altered targeting of P0, may be responsible for CH, and that different types of gain of abnormal function produce the diverse neuropathy phenotypes associated with MPZ, supporting future allele-specific therapeutic silencing strategies.
蛋白零(P0)是周围髓鞘的主要结构蛋白,而髓鞘蛋白零(Mpz)基因的突变会产生广泛的遗传性神经病表型。为了深入了解一种特别严重形式——先天性髓鞘发育不良(CH)的发病机制,我们将小鼠 Mpz 靶向编码 P0Q215X,这是一种与该疾病相关的无义突变,我们发现它逃避了无义介导的衰变,并在 CH 患者神经中表达。敲入小鼠表达低水平的截短蛋白,与患者相比表现出较轻的表型,这使得我们能够剖析在其他非常受损的周围髓鞘中发生的微妙的致病机制。我们发现 P0Q215X 不会引发未折叠蛋白反应,这是其他致病性 MPZ 突变的关键机制,但部分异常地转运到非髓鞘质质膜,并诱导施万细胞对轴突的放射状分选缺陷。我们表明,C 端 Tyr-Ala-Met-Leu 基序的缺失是 P0 定位错误的原因,因为其添加能够在体外恢复正确的 P0Q215X 转运。最后,我们表明 P0Q215X 通过异常功能的剂量依赖性获得发挥作用,因为野生型 P0 无法挽救低髓鞘表型。总的来说,这些数据表明,在前期髓鞘形成阶段发生的改变,与 P0 靶向改变有关,可能是 CH 的原因,而不同类型的异常功能获得会产生与 MPZ 相关的各种神经病表型,支持未来针对特定等位基因的治疗性沉默策略。