不间断
核糖体
生物
遗传学
闪耀达尔加诺序列
线粒体核糖体
核糖体分析
翻译(生物学)
基因
起始密码子
信使核糖核酸
计算生物学
粒线体疾病
线粒体DNA
细胞生物学
核糖核酸
计算机科学
操作系统
作者
Kah Ying Ng,Guleycan Lutfullahoglu Bal,Uwe Richter,Omid Safronov,Lars Paulin,Cory D. Dunn,Ville O. Paavilainen,Julie Richer,William G. Newman,Robert W. Taylor,Brendan J. Battersby
标识
DOI:10.1126/sciadv.abq5234
摘要
A stop codon within the mRNA facilitates coordinated termination of protein synthesis, releasing the nascent polypeptide from the ribosome. This essential step in gene expression is impeded with transcripts lacking a stop codon, generating nonstop ribosome complexes. Here, we use deep sequencing to investigate sources of nonstop mRNAs generated from the human mitochondrial genome. We identify diverse types of nonstop mRNAs on mitochondrial ribosomes that are resistant to translation termination by canonical release factors. Failure to resolve these aberrations by the mitochondrial release factor in rescue (MTRFR) imparts a negative regulatory effect on protein synthesis that is associated with human disease. Our findings reveal a source of underlying noise in mitochondrial gene expression and the importance of responsive ribosome quality control mechanisms for cell fitness and human health.
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