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Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC)

Reactome ID: R-HSA-975956

中文名称

无义介导的降解(NMD),与外显子连接复合物(EJC)无关

通路描述

观察到无义介导的降解(NMD)发生在没有终止密码子下游外显子连接复合物(EJC)的mRNA上(参见Isken和Maquat, 2007; Chang等, 2007; Behm-Ansmant等, 2007; Rebbapragada和Lykke-Andersen, 2009; Nicholson等, 2010)。在这些情况下,触发机制尚不清楚,但有时观察到3' UTR长度的相关性。当前模型认为PABP和UPF1在终止核糖体处竞争以访问eRF3(Ivanov等, 2008; Singh等, 2008,参见Bhuvanagiri等, 2010)。异常长的3' UTR可能阻止PABP与eRF3高效相互作用,允许UPF1结合eRF3。带有发夹环的长UTR可能将PABP带得更近于eRF3,并帮助逃避NMD(Eberle等, 2008)。EJC无关NMD的降解途径尚未阐明。认为UPF1的磷酸化由SMG1介导,SMG6或SMG5和SMG7的招募参与其中,这与EJC增强型NMD类似,但尚未证明。
英文描述
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) Nonsense-mediated decay has been observed with mRNAs that do not have an exon junction complex (EJC) downstream of the termination codon (reviewed in Isken and Maquat 2007, Chang et al. 2007, Behm-Ansmant et al. 2007, Rebbapragada and Lykke-Andersen 2009, Nicholson et al. 2010). In these cases the trigger is unknown but a correlation with the length of the 3' UTR has sometimes been seen. The current model posits a competition between PABP and UPF1 for access to eRF3 at the terminating ribosome (Ivanov et al. 2008, Singh et al. 2008, reviewed in Bhuvanagiri et al. 2010). Abnormally long 3' UTRs may prevent PABP from efficiently interacting with eRF3 and allow UPF1 to bind eRF3 instead. Long UTRs with hairpin loops may bring PABP closer to eRF3 and help evade NMD (Eberle et al. 2008).
The pathway of degradation taken during EJC-independent NMD has not been elucidated. It is thought that phosphorylation of UPF1 by SMG1 and recruitment of SMG6 or SMG5 and SMG7 are involved, as with EJC-enhanced NMD, but this has not yet been shown.

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