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August 1, 2002Journal of Cell Science242 citations

mRNA surveillance: the perfect persist

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EWEileen WagnerJLJens Lykke‐Andersen

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Abstract

In eukaryotes, an elaborate set of mechanisms has evolved to ensure that the multistep process of gene expression is accurately executed and adapted to cellular needs. The mRNA surveillance pathway works in this context by assessing the quality of mRNAs to ensure that they are suitable for translation. mRNA surveillance facilitates the detection and destruction of mRNAs that contain premature termination codons by a process called nonsense-mediated decay. Moreover, recent studies have shown that a distinct mRNA surveillance process, called nonstop decay, is responsible for depleting mRNAs that lack in-frame termination codons. mRNA surveillance thereby prevents the synthesis of truncated and otherwise aberrant proteins, which can have dominant-negative and other deleterious effects.

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Cite This Study

Wagner et al. (2002) studied this question.

synapsesocial.com/papers/6a1928ae2471b46e09d954f4https://doi.org/10.1242/jcs.115.15.3033
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Human Upf Proteins Target an mRNA for Nonsense-Mediated Decay When Bound Downstream of a Termination Codon2000 · 589 citations
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  4. 4The role of Upf proteins in modulating the translation read‐through of nonsense‐containing transcripts2001 · 218 citations
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