Department of Natural and Applied Sciences, University of Dubai, P.O.Box: 14143, Academic City, Dubai, United Arab Emirates.
Department of Pathology, College of Medicine and Health Sciences, United Arab Emirates University, Al-Ain, Abu Dhabi, United Arab Emirates.
Mol Med. 2019 Dec 31;26(1):4. doi: 10.1186/s10020-019-0129-7.
The ER is hub for protein folding. Proteins that harbor a Frizzled cysteine-rich domain (FZ-CRD) possess 10 conserved cysteine motifs held by a unique disulfide bridge pattern which attains a correct fold in the ER. Little is known about implications of disease-causing missense mutations within FZ-CRD families. Mutations in FZ-CRD of Frizzled class receptor 4 (FZD4) and Muscle, skeletal, receptor tyrosine kinase (MuSK) and Receptor tyrosine kinase-like orphan receptor 2 (ROR2) cause Familial Exudative Vitreoretinopathy (FEVR), Congenital Myasthenic Syndrome (CMS), and Robinow Syndrome (RS) respectively. We highlight reported pathogenic inherited missense mutations in FZ-CRD of FZD4, MuSK and ROR2 which misfold, and traffic abnormally in the ER, with ER-associated degradation (ERAD) as a common pathogenic mechanism for disease. Our review shows that all studied FZ-CRD mutants of RS, FEVR and CMS result in misfolded proteins and/or partially misfolded proteins with an ERAD fate, thus we coin them as "disorders of FZ-CRD". Abnormal trafficking was demonstrated in 17 of 29 mutants studied; 16 mutants were within and/or surrounding the FZ-CRD with two mutants distant from FZ-CRD. These ER-retained mutants were improperly N-glycosylated confirming ER-localization. FZD4 and MuSK mutants were tagged with polyubiquitin chains confirming targeting for proteasomal degradation. Investigating the cellular and molecular mechanisms of these mutations is important since misfolded protein and ER-targeted therapies are in development. The P344R-MuSK kinase mutant showed around 50% of its in-vitro autophosphorylation activity and P344R-MuSK increased two-fold on proteasome inhibition. M105T-FZD4, C204Y-FZD4, and P344R-MuSK mutants are thermosensitive and therefore, might benefit from extending the investigation to a larger number of chemical chaperones and/or proteasome inhibitors. Nonetheless, FZ-CRD ER-lipidation it less characterized in the literature and recent structural data sheds light on the importance of lipidation in protein glycosylation, proper folding, and ER trafficking. Current treatment strategies in-place for the conformational disease landscape is highlighted. From this review, we envision that disorders of FZ-CRD might be receptive to therapies that target FZ-CRD misfolding, regulation of fatty acids, and/or ER therapies; thus paving the way for a newly explored paradigm to treat different diseases with common defects.
内质网是蛋白质折叠的中心。含有卷曲螺旋富含半胱氨酸结构域(FZ-CRD)的蛋白质具有 10 个保守的半胱氨酸模体,由独特的二硫键模式维持,在 ER 中获得正确的折叠。关于 FZ-CRD 家族中致病错义突变的影响知之甚少。卷曲受体 4(FZD4)和肌肉、骨骼、受体酪氨酸激酶(MuSK)和受体酪氨酸激酶样孤儿受体 2(ROR2)的 FZ-CRD 中的突变分别导致家族性渗出性玻璃体视网膜病变(FEVR)、先天性肌无力综合征(CMS)和罗宾诺综合征(RS)。我们强调了报道的 FZD4、MuSK 和 ROR2 的 FZ-CRD 中致病性遗传错义突变,这些突变在内质网中错误折叠和异常运输,内质网相关降解(ERAD)是疾病的共同致病机制。我们的综述表明,所有研究的 RS、FEVR 和 CMS 的 FZ-CRD 突变体导致错误折叠的蛋白质和/或部分错误折叠的蛋白质具有 ERAD 命运,因此我们将它们命名为“FZ-CRD 疾病”。在研究的 29 个突变体中,有 17 个显示异常转运;16 个突变体位于 FZ-CRD 内和/或周围,两个突变体远离 FZ-CRD。这些在内质网中保留的突变体未正确进行 N-糖基化,证实了内质网定位。FZD4 和 MuSK 突变体被多聚泛素链标记,证实了针对蛋白酶体降解的靶向。研究这些突变的细胞和分子机制非常重要,因为错误折叠的蛋白质和内质网靶向治疗正在开发中。P344R-MuSK 激酶突变体显示约 50%的体外自身磷酸化活性,P344R-MuSK 在蛋白酶体抑制时增加两倍。M105T-FZD4、C204Y-FZD4 和 P344R-MuSK 突变体是热敏的,因此可能受益于将研究扩展到更多的化学伴侣和/或蛋白酶体抑制剂。尽管如此,FZ-CRD 在内质网中的脂化作用在文献中描述得较少,最近的结构数据揭示了脂化在蛋白质糖基化、正确折叠和内质网运输中的重要性。突出了目前针对构象疾病的治疗策略。从本综述中,我们设想 FZ-CRD 疾病可能对针对 FZ-CRD 错误折叠、脂肪酸调节和/或内质网治疗的治疗方法有反应;从而为用共同缺陷治疗不同疾病开辟了一个新的探索范式。