Laboratori of Neuromuscular and Mitochondrial Disorders, Universitat Autònoma de Barcelona, Barcelona, Spain.
Hum Mutat. 2011 Apr;32(4):E2061-8. doi: 10.1002/humu.21447. Epub 2011 Jan 18.
The cellular quality control systems enable surveillance and selective degradation of nonsense, nonstop, and no-go mRNAs. In the case of nonstop mRNA, different mechanisms of nonstop-mediated decay (NSD) have been described for bacteria, yeast and mammals, but the molecular consequences of nonstop mutations have been examined in only few cases of human disease. We describe a novel homozygous nonstop mRNA mutation (c.1416delC) in the TYMP gene encoding thymidine phosphorylase, in a patient with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE). In contrast to previous reports showing selective decay of pathogenic nonstop mRNAs, quantitative real-time PCR and 3'-RACE-RFLP analysis revealed unreduced nonstop mRNA levels in our patient and 2 heterozygous carriers of the mutation. The absence of thymidine phosphorylase protein in the homozygous patient, together with the partial decrease in levels of this protein in 2 carriers suggest that the main control system in this case resides at the translational or post-translational levels rather than through NSD. This is the first report showing an absence of NSD in a human disease, revealing that this surveillance mechanism has exceptions in vivo.
细胞质量控制系统能够监控和选择性降解无义、无终止和无意义的 mRNA。在无终止 mRNA 的情况下,细菌、酵母和哺乳动物已经描述了不同的无终止介导的降解 (NSD) 机制,但无终止突变的分子后果仅在少数人类疾病病例中进行了研究。我们描述了一种新的纯合无终止 mRNA 突变 (c.1416delC),位于编码胸苷磷酸化酶的 TYMP 基因中,该突变存在于一名患有线粒体神经胃肠脑肌病 (MNGIE) 的患者中。与先前的报告显示致病性无终止 mRNA 选择性降解不同,定量实时 PCR 和 3'-RACE-RFLP 分析显示我们的患者和 2 名突变杂合携带者的无终止 mRNA 水平没有减少。纯合子患者中缺乏胸苷磷酸化酶蛋白,而 2 名携带者中该蛋白水平部分下降表明,在这种情况下,主要的控制机制位于翻译或翻译后水平,而不是通过 NSD。这是第一个报告显示在人类疾病中不存在 NSD 的报告,揭示了这种监控机制在体内存在例外。