Department of Biochemistry an Molecular Genetics, University of Illinois at Chicago, Chicago, Illinois 60607, USA.
Laboratory of Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Sci Rep. 2016 Aug 31;6:32563. doi: 10.1038/srep32563.
Selenocysteine synthase (SepSecS) catalyzes the terminal reaction of selenocysteine, and is vital for human selenoproteome integrity. Autosomal recessive inheritance of mutations in SepSecS-Ala239Thr, Thr325Ser, Tyr334Cys and Tyr429*-induced severe, early-onset, neurological disorders in distinct human populations. Although harboring different mutant alleles, patients presented remarkably similar phenotypes typified by cerebellar and cerebral atrophy, seizures, irritability, ataxia, and extreme spasticity. However, it has remained unclear how these genetic alterations affected the structure of SepSecS and subsequently elicited the development of a neurological pathology. Herein, our biophysical and structural characterization demonstrates that, with the exception of Tyr429*, pathogenic mutations decrease protein stability and trigger protein misfolding. We propose that the reduced stability and increased propensity towards misfolding are the main causes for the loss of SepSecS activity in afflicted patients, and that these factors contribute to disease progression. We also suggest that misfolding of enzymes regulating protein synthesis should be considered in the diagnosis and study of childhood neurological disorders.
硒代半胱氨酸合酶(SepSecS)催化硒代半胱氨酸的末端反应,对人类硒蛋白组的完整性至关重要。SepSecS-Ala239Thr、Thr325Ser、Tyr334Cys 和 Tyr429*-诱导的突变以常染色体隐性遗传方式在不同人群中引起严重的早发性神经疾病。尽管携带不同的突变等位基因,但患者表现出明显相似的表型,特征为小脑和大脑萎缩、癫痫发作、易怒、共济失调和极度痉挛。然而,这些遗传改变如何影响 SepSecS 的结构并随后引发神经病理学的发展仍不清楚。在此,我们的生物物理和结构表征表明,除了 Tyr429*,致病性突变会降低蛋白质稳定性并引发蛋白质错误折叠。我们提出,在受影响的患者中,SepSecS 活性丧失的主要原因是稳定性降低和错误折叠倾向增加,这些因素导致疾病进展。我们还建议在儿童神经疾病的诊断和研究中应考虑调节蛋白质合成的酶的错误折叠。