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When a ribosome encounters a premature termination codon

Journal

BMB REPORTS
Volume 46, Issue 1, Pages 9-16

Publisher

KOREAN SOCIETY BIOCHEMISTRY & MOLECULAR BIOLOGY
DOI: 10.5483/BMBRep.2013.46.1.002

Keywords

NAS; NMD; NMTGS; NMTR; PTC

Funding

  1. National Research Foundation of Korea (NRF)
  2. Ministry of Education, Science and Technology [2012R1A2A1A01002469]
  3. Hanyang University [HY-2011-N]
  4. National Research Foundation of Korea [2012R1A2A1A01002469] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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In mammalian cells, aberrant transcripts harboring a premature termination codon (PTC) can be generated by abnormal or inefficient biogenesis of mRNAs or by somatic mutation. Truncated polypeptides synthesized from these aberrant transcripts could be toxic to normal cellular functions. However, mammalian cells have evolved sophisticated mechanisms for monitoring the quality of mRNAs. The faulty transcripts harboring PTC are subject to nonsense-mediated mRNA decay (NMD), nonsense-mediated translational repression (NMTR), nonsense-associated alternative splicing (NAS), or nonsense-mediated transcriptional gene silencing (NMTGS). In this review, we briefly outline the molecular characteristics of each pathway and suggest mRNA quality control mechanisms as a means to regulate normal gene expression. [BMB Reports 2013; 46(1): 9-16]

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