Literature DB >> 16757948

Nonsense-mediated mRNA decay modulates clinical outcome of genetic disease.

Mehrdad Khajavi1, Ken Inoue, James R Lupski.   

Abstract

The nonsense-mediated decay (NMD) pathway is an mRNA surveillance system that typically degrades transcripts containing premature termination codons (PTCs) in order to prevent translation of unnecessary or aberrant transcripts. Failure to eliminate these mRNAs with PTCs may result in the synthesis of abnormal proteins that can be toxic to cells through dominant-negative or gain-of-function effects. Recent studies have expanded our understanding of the mechanism by which nonsense transcripts are recognized and targeted for decay. Here, we review the physiological role of this surveillance pathway, its implications for human diseases, and why knowledge of NMD is important to an understanding of genotype-phenotype correlations in various genetic disorders.

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Year:  2006        PMID: 16757948     DOI: 10.1038/sj.ejhg.5201649

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  170 in total

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3.  Transcobalamin deficiency caused by compound heterozygosity for two novel mutations in the TCN2 gene: a study of two affected siblings, their brother, and their parents.

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4.  Chediak-Higashi syndrome with early developmental delay resulting from paternal heterodisomy of chromosome 1.

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Journal:  Am J Med Genet A       Date:  2010-06       Impact factor: 2.802

Review 5.  Nonsense-mediated mRNA decay: an intricate machinery that shapes transcriptomes.

Authors:  Søren Lykke-Andersen; Torben Heick Jensen
Journal:  Nat Rev Mol Cell Biol       Date:  2015-09-23       Impact factor: 94.444

6.  FAM92A Underlies Nonsyndromic Postaxial Polydactyly in Humans and an Abnormal Limb and Digit Skeletal Phenotype in Mice.

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Journal:  J Bone Miner Res       Date:  2018-11-05       Impact factor: 6.741

7.  Stop-codon and C-terminal nonsense mutations are associated with a lower risk of cardiac events in patients with long QT syndrome type 1.

Authors:  Martin H Ruwald; Xiaorong Xu Parks; Arthur J Moss; Wojciech Zareba; Jayson Baman; Scott McNitt; Jorgen K Kanters; Wataru Shimizu; Arthur A Wilde; Christian Jons; Coeli M Lopes
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Review 8.  Therapeutics based on stop codon readthrough.

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Journal:  Annu Rev Genomics Hum Genet       Date:  2014-04-18       Impact factor: 8.929

Review 9.  Nonsense-mediated decay in genetic disease: friend or foe?

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Journal:  Mutat Res Rev Mutat Res       Date:  2014-05-28       Impact factor: 5.657

10.  CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta.

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Journal:  Hum Mutat       Date:  2008-12       Impact factor: 4.878

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