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Nonsense-mediated mRNA decay in Tetrahymena is EJC independent and requires a protozoa-specific nuclease

机译:无意义的介导的mRNA衰减在四环塞中是EJC独立的,需要一种特异性特异性核酸酶

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Nonsense-mediated mRNA decay (NMD) is essential for removing premature termination co-doncontaining transcripts from cells. Studying the NMD pathway in model organisms can help to elucidate the NMD mechanism in humans and improve our understanding of how this biologically important process has evolved. Ciliates are among the earliest branching eukaryotes; their NMD mechanism is poorly understood and may be primordial. We demonstrate that highly conserved Upf proteins (Upf1a, Upf2 and Upf3) are involved in the NMD pathway of the ciliate, Tetrahymena thermophila. We further show that a novel protozoa-specific nuclease, Smg6L, is responsible for destroying many NMD-targeted transcripts. Transcriptome-wide identification and characterization of NMD-targeted transcripts in vegetative Tetrahymena cells showed that many have exon-exon junctions downstream of the termination codon. However, Tetrahymena may lack a functional exon junction complex (EJC), and the Tetrahymena ortholog of an EJC core component, Mago nashi (Mag1), is dispensable for NMD. Therefore, NMD is EJC independent in this early branching eukaryote.
机译:无意义介导的mRNA衰减(NMD)对于从细胞中去除过早终止转录转录物至关重要。研究模型生物中的NMD途径可以帮助阐明人类的NMD机制,提高我们对这种生物学重要的过程如何发展的理解。 Ciliates是最早的分支真核区之一;他们的NMD机制很差,可能是原始的。我们证明高度保守的UPF蛋白(UPF1A,UPF2和UPF3)涉及CiLiate,Tetrahymena Thermophila的NMD途径。我们进一步表明,一种新型原生动物特异性核酸酶SMG6L,负责破坏许多NMD靶向的转录物。在营养四氢钠细胞中的NMD靶向转录物的转录物覆盖和表征显示,许多终止密码子下游的外显子连接。然而,Tetrahymena可能缺乏功能性外显子结综合体(EJC),并且EJC核心组分的Tetrahymena Ortholog Mago Nashi(Mag1)可用于NMD。因此,NMD在这种早期分支的真核生物中独立于EJC。

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