Attenuated Codon Optimality Contributes to Neural-Specific mRNA Decay in Drosophila
Cell Reports, ISSN: 2211-1247, Vol: 24, Issue: 7, Page: 1704-1712
2018
- 47Citations
- 87Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations47
- Citation Indexes47
- 47
- CrossRef44
- Captures87
- Readers87
- 87
Article Description
Tissue-specific mRNA stability is important for cell fate and physiology, but the mechanisms involved are not fully understood. We found that zygotic mRNA stability in Drosophila correlates with codon content: optimal codons are enriched in stable transcripts associated with metabolic functions like translation, while non-optimal codons are enriched in unstable transcripts, including those associated with neural development. Bioinformatic analyses and reporter assays revealed that similar codons stabilize or destabilize mRNAs in the nervous system and other tissues, but the link between codon content and stability is attenuated in the nervous system. We confirmed that optimal codons are decoded by abundant tRNAs while non-optimal codons are decoded by less abundant tRNAs in embryos and in the nervous system. We conclude that codon optimality is a general determinant of zygotic mRNA stability, and attenuation of codon optimality allows trans -acting factors to exert greater influence over mRNA decay in the nervous system.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S221112471831129X; http://dx.doi.org/10.1016/j.celrep.2018.07.039; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85051029744&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/30110627; https://linkinghub.elsevier.com/retrieve/pii/S221112471831129X; https://dx.doi.org/10.1016/j.celrep.2018.07.039
Elsevier BV
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