Computational Biology Program, Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Basic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Life Sci Alliance. 2021 Dec 8;5(3). doi: 10.26508/lsa.202101217. Print 2022 Mar.
Nonsense-mediated mRNA decay (NMD) is an essential, highly conserved quality control pathway that detects and degrades mRNAs containing premature termination codons. Although the essentiality of NMD is frequently ascribed to its prevention of truncated protein accumulation, the extent to which NMD actually suppresses proteins encoded by NMD-sensitive transcripts is less well-understood than NMD-mediated suppression of mRNA. Here, we describe a reporter system that permits accurate quantification of both mRNA and protein levels via stable integration of paired reporters encoding NMD-sensitive and NMD-insensitive transcripts into the AAVS1 safe harbor loci in human cells. We use this system to demonstrate that NMD suppresses proteins encoded by NMD-sensitive transcripts by up to eightfold more than the mRNA itself. Our data indicate that NMD limits the accumulation of proteins encoded by NMD substrates by mechanisms beyond mRNA degradation, such that even when NMD-sensitive mRNAs escape destruction, their encoded proteins are still effectively suppressed.
无意义介导的 mRNA 降解 (NMD) 是一种重要的、高度保守的质量控制途径,可检测和降解含有提前终止密码子的 mRNA。尽管 NMD 的必要性通常归因于其防止截断蛋白的积累,但 NMD 实际上抑制 NMD 敏感转录本编码的蛋白的程度,不如 NMD 对 mRNA 的抑制程度那么为人所知。在这里,我们描述了一种报告系统,通过将编码 NMD 敏感和 NMD 不敏感转录本的配对报告基因稳定整合到人类细胞的 AAVS1 安全港基因座中,可通过稳定整合来准确量化 mRNA 和蛋白水平。我们利用该系统证明,NMD 对 NMD 敏感转录本编码的蛋白的抑制作用比 mRNA 本身高出多达 8 倍。我们的数据表明,NMD 通过超越 mRNA 降解的机制来限制 NMD 底物编码蛋白的积累,即使 NMD 敏感的 mRNA 逃脱破坏,其编码的蛋白仍然被有效地抑制。