Department of Pediatrics, University of Wisconsin-Madison , Madison, Wisconsin.
Department of Cell and Regenerative Biology, University of Wisconsin-Madison , Madison, Wisconsin.
Am J Physiol Heart Circ Physiol. 2018 Jun 1;314(6):H1179-H1191. doi: 10.1152/ajpheart.00686.2017. Epub 2018 Feb 16.
Cardiac myosin-binding protein C (cMyBP-C) is a functional sarcomeric protein that regulates contractility in response to contractile demand, and many mutations in cMyBP-C lead to hypertrophic cardiomyopathy (HCM). To gain insight into the effects of disease-causing cMyBP-C missense mutations on contractile function, we expressed the pathogenic W792R mutation (substitution of a highly conserved tryptophan residue by an arginine residue at position 792) in mouse cardiomyocytes lacking endogenous cMyBP-C and studied the functional effects using three-dimensional engineered cardiac tissue constructs (mECTs). Based on complete conservation of tryptophan at this location in fibronectin type II (FnIII) domains, we hypothesized that the W792R mutation affects folding of the C6 FnIII domain, destabilizing the mutant protein. Adenoviral transduction of wild-type (WT) and W792R cDNA achieved equivalent mRNA transcript abundance, but not equivalent protein levels, with W792R compared with WT controls. mECTs expressing W792R demonstrated abnormal contractile kinetics compared with WT mECTs that were nearly identical to cMyBP-C-deficient mECTs. We studied whether common pathways of protein degradation were responsible for the rapid degradation of W792R cMyBP-C. Inhibition of both ubiquitin-proteasome and lysosomal degradation pathways failed to increase full-length mutant protein abundance to WT equivalence, suggesting rapid cytosolic degradation. Bacterial expression of WT and W792R protein fragments demonstrated decreased mutant stability with altered thermal denaturation and increased susceptibility to trypsin digestion. These data suggest that the W792R mutation destabilizes the C6 FnIII domain of cMyBP-C, resulting in decreased full-length protein expression. This study highlights the vulnerability of FnIII-like domains to mutations that alter domain stability and further indicates that missense mutations in cMyBP-C can cause disease through a mechanism of haploinsufficiency. NEW & NOTEWORTHY This study is one of the first to describe a disease mechanism for a missense mutation in cardiac myosin-binding protein C linked to hypertrophic cardiomyopathy. The mutation decreases stability of the fibronectin type III domain and results in substantially reduced mutant protein expression dissonant to transcript abundance.
心肌肌球蛋白结合蛋白 C(cMyBP-C)是一种功能性肌节蛋白,可响应收缩需求调节收缩性,许多 cMyBP-C 突变可导致肥厚型心肌病(HCM)。为了深入了解致病的 cMyBP-C 错义突变对收缩功能的影响,我们在缺乏内源性 cMyBP-C 的小鼠心肌细胞中表达了致病性 W792R 突变(在位置 792 处用精氨酸取代高度保守的色氨酸残基),并使用三维工程心脏组织构建体(mECT)研究了功能影响。基于纤维连接蛋白 II 型(FnIII)结构域中色氨酸的完全保守性,我们假设 W792R 突变影响 C6 FnIII 结构域的折叠,使突变蛋白不稳定。野生型(WT)和 W792R cDNA 的腺病毒转导实现了相当的 mRNA 转录丰度,但与 WT 对照相比,W792R 的蛋白水平并不相当。与 WT mECT 相比,表达 W792R 的 mECT 显示出异常的收缩动力学,几乎与缺乏 cMyBP-C 的 mECT 相同。我们研究了是否常见的蛋白降解途径导致 W792R cMyBP-C 的快速降解。抑制泛素-蛋白酶体和溶酶体降解途径都未能使全长突变蛋白的丰度增加到 WT 等效水平,表明存在快速的细胞质降解。WT 和 W792R 蛋白片段的细菌表达显示突变体稳定性降低,热变性改变,对胰蛋白酶消化的敏感性增加。这些数据表明,W792R 突变使 cMyBP-C 的 C6 FnIII 结构域不稳定,导致全长蛋白表达减少。这项研究强调了 FnIII 样结构域对改变结构域稳定性的突变的脆弱性,并进一步表明 cMyBP-C 中的错义突变可以通过杂合不足的机制导致疾病。本研究是首次描述与肥厚型心肌病相关的心肌肌球蛋白结合蛋白 C 中的错义突变的疾病机制之一。该突变降低了纤维连接蛋白 III 结构域的稳定性,导致突变蛋白的表达显著减少,与转录丰度不一致。