Results 41 to 50 of about 270,897 (278)

Synthetic Approach to Stop-Codon Scanning Mutagenesis [PDF]

open access: yesJournal of the American Chemical Society, 2011
A general combinatorial mutagenesis strategy using common dimethoxytrityl-protected mononucleotide phosphoramidites and a single orthogonally protected trinucleotide phosphoramidite (Fmoc-TAG; Fmoc = 9-fluorenylmethoxycarbonyl) was developed to scan a gene with the TAG amber stop codon with complete synthetic control.
Lihua, Nie   +4 more
openaire   +2 more sources

Selection for tandem stop codons in ciliate species with reassigned stop codons

open access: yesPLOS ONE, 2019
The failure of mRNA translation machinery to recognize a stop codon as a termination signal and subsequent translation of the 3' untranslated region (UTR) is referred to as stop codon readthrough, the frequency of which is related to the length, composition, and structure of mRNA sequences downstream of end-of-gene stop codons.
Ira Fleming, Andre R. O. Cavalcanti
openaire   +4 more sources

Stop codon reassignments in the wild

open access: yesScience, 2014
The canonical genetic code is assumed to be deeply conserved across all domains of life with very few exceptions. By scanning 5.6 trillion base pairs of metagenomic data for stop codon reassignment events, we detected recoding in a substantial fraction of the >1700 environmental samples examined. We observed extensive opal
ivanova, Natalia   +9 more
openaire   +3 more sources

Karyorelict ciliates use an ambiguous genetic code with context-dependent stop/sense codons

open access: yesPeer Community Journal, 2022
In ambiguous stop/sense genetic codes, the stop codon(s) not only terminate translation but can also encode amino acids. Such codes have evolved at least four times in eukaryotes, twice among ciliates (Condylostoma magnum and Parduczia sp.).
Seah, Brandon Kwee Boon   +2 more
doaj   +1 more source

Directional Next-Generation RNA Sequencing and Examination of Premature Termination Codon Mutations in Endoglin/Hereditary Haemorrhagic Telangiectasia [PDF]

open access: yes, 2012
Hereditary haemorrhagic telangiectasia (HHT) is a disease characterised by abnormal vascular structures, and most commonly caused by mutations in ENG, ACVRL1 or SMAD4 encoding endothelial cell-expressed proteins involved in TGF-β superfamily signalling ...
Begbie, ME   +6 more
core   +1 more source

Evolutionary Dynamics of Abundant Stop Codon Readthrough [PDF]

open access: yesMolecular Biology and Evolution, 2016
Translational stop codon readthrough emerged as a major regulatory mechanism affecting hundreds of genes in animal genomes, based on recent comparative genomics and ribosomal profiling evidence, but its evolutionary properties remain unknown. Here, we leverage comparative genomic evidence across 21 Anopheles mosquitoes to systematically annotate ...
Fields, Gabriel   +5 more
openaire   +5 more sources

Versatile dual reporter gene systems for investigating stop codon readthrough in plants. [PDF]

open access: yesPLoS ONE, 2009
Translation is most often terminated when a ribosome encounters the first in-frame stop codon (UAA, UAG or UGA) in an mRNA. However, many viruses (and some cellular mRNAs) contain "stop" codons that cause a proportion of ribosomes to terminate and others
Nga T Lao   +3 more
doaj   +1 more source

Codon-biased translation can be regulated by wobble-base tRNA modification systems during cellular stress responses [PDF]

open access: yes, 2014
tRNA (tRNA) is a key molecule used for protein synthesis, with multiple points of stress-induced regulation that can include transcription, transcript processing, localization and ribonucleoside base modification.
Begley, Thomas J.   +2 more
core   +1 more source

Selection Shapes Synonymous Stop Codon Use in Mammals [PDF]

open access: yesJournal of Molecular Evolution, 2019
AbstractPhylogenetic models of the evolution of protein-coding sequences can provide insights into the selection pressures that have shaped them. In the application of these models synonymous nucleotide substitutions, which do not alter the encoded amino acid, are often assumed to have limited functional consequences and used as a proxy for the neutral
Seoighe, Cathal   +4 more
openaire   +4 more sources

Statistical analysis of readthrough levels for nonsense mutations in mammalian cells reveals a major determinant of response to gentamicin. [PDF]

open access: yesPLoS Genetics, 2012
The efficiency of translation termination depends on the nature of the stop codon and the surrounding nucleotides. Some molecules, such as aminoglycoside antibiotics (gentamicin), decrease termination efficiency and are currently being evaluated for ...
Célia Floquet   +3 more
doaj   +1 more source

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