Department of Dermatology and Allergology, University Hospital of the Paracelsus Medical University, 5020 Salzburg, Austria.
Department of Biosciences, University of Salzburg, 5020 Salzburg, Austria.
Int J Mol Sci. 2023 Mar 23;24(7):6101. doi: 10.3390/ijms24076101.
Nonsense mutations trigger premature translation termination and often give rise to prevalent and rare genetic diseases. Consequently, the pharmacological suppression of an unscheduled stop codon represents an attractive treatment option and is of high clinical relevance. At the molecular level, the ability of the ribosome to continue translation past a stop codon is designated stop codon readthrough (SCR). SCR of disease-causing premature termination codons (PTCs) is minimal but small molecule interventions, such as treatment with aminoglycoside antibiotics, can enhance its frequency. In this review, we summarize the current understanding of translation termination (both at PTCs and at cognate stop codons) and highlight recently discovered pathways that influence its fidelity. We describe the mechanisms involved in the recognition and readthrough of PTCs and report on SCR-inducing compounds currently explored in preclinical research and clinical trials. We conclude by reviewing the ongoing attempts of personalized nonsense suppression therapy in different disease contexts, including the genetic skin condition epidermolysis bullosa.
无义突变会引发过早的翻译终止,并常常导致常见和罕见的遗传疾病。因此,抑制无义密码子的药理学方法代表了一种有吸引力的治疗选择,具有很高的临床相关性。在分子水平上,核糖体继续翻译终止密码子的能力被指定为终止密码子通读(SCR)。导致疾病的终止密码子(PTC)的 SCR 很少,但小分子干预,如使用氨基糖苷类抗生素治疗,可以提高其频率。在这篇综述中,我们总结了目前对翻译终止(包括 PTC 和同源终止密码子)的理解,并强调了最近发现的影响其保真度的途径。我们描述了 PTC 识别和通读所涉及的机制,并报告了目前在临床前研究和临床试验中探索的 SCR 诱导化合物。最后,我们回顾了在不同疾病背景下进行的个性化无义抑制治疗的持续尝试,包括遗传皮肤疾病大疱性表皮松解症。