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Charles, B.

Publications and source records attributed to Charles, B..

3 recordsLinked to original sources

Varied forms of mutant tRNA mistranslation produce distinct phenotypes across multiple model organisms

Mutant tRNA mistranslation is a phenomena in which specific tRNA gene mutations cause translational errors wherein amino acids incorporated during translation differ from those coded by mRNA sequences. The biological consequences of mutant tRNA mistranslation are highly complex and contextual, but are often deleterious. Importantly, many variables exist that are likely to affect the outcomes of any one mutant mistranslating tRNA; biochemical characteristics of the exchanged amino acids, frequency of use, identity of mistranslated products, and so on. Here, we generate a carefully curated array of tRNA mutants to assess which characteristics of mistranslating tRNA variants are most predictive of deleterious phenotypes. We find that toxicity often arises from mutant tRNAs that induce dramatic changes in biochemical properties between exchanged amino acids, as well as mistranslation that occurs more frequently. Importantly, exceptions are also observed to each of these general rules, implying instead that some deliriousness may arise from more granular, product-specific mechanisms. Additionally, quantification of mistranslation via mass spectrometry demonstrates a weak relationship between quantity of mistranslated products and severity of toxic phenotypes. Lastly, despite previous establishment of mutant mistranslating tRNA models in Drosophila melanogaster, incorporation of higher frequency mistranslating tRNA variants was largely unsuccessful, and incorporation of lower frequency mistranslating tRNA variants produces no detectable developmental phenotypes. These experiments support the notion that although general rules may be capable of reasonably predicting their consequences, each mistranslating tRNA variant warrants individual consideration and investigation for thorough understanding of its biological outcomes and precise mechanisms of toxicity.

genetics↗

Mistranslating tRNA variants have anticodon- and sex-specific impacts on Drosophila melanogaster

Transfer RNAs (tRNAs) are vital in determining the specificity of translation. Mutations in tRNA genes can result in the misincorporation of amino acids into nascent polypeptides in a process known as mistranslation. Since mistranslation has different impacts, depending on the type of amino acid substitution, our goal here was to compare the impact of different mistranslating tRNASer variants on fly development, lifespan, and behaviour. We established two mistranslating fly lines, one with a tRNASer variant that misincorporates serine at valine codons (VS) and the other that misincorporates serine at threonine codons (TaS). While both mistranslating tRNAs increased development time and developmental lethality, the severity of the impacts differed depending on amino acid substitution and sex. The VS variant extended embryonic, larval, and pupal development whereas the TS only extended larval and pupal development. Females, but not males, containing either mistranslating tRNA presented with significantly more anatomical deformities than controls. Mistranslating females also experienced extended lifespan whereas mistranslating male lifespan was unaffected. In addition, mistranslating flies from both sexes showed improved locomotion as they aged, suggesting delayed neurodegeneration. Therefore, although mistranslation causes detrimental effects, we demonstrate that mistranslation also has positive effects on complex traits such as lifespan and locomotion. This has important implications for human health given the prevalence of tRNA variants in humans. PLAIN LANGUAGE SUMMARYMutant tRNA genes can cause mistranslation, the misincorporation of amino acids into proteins, and are associated with several human diseases. This study investigated the role of two tRNA variants that cause threonine-to-serine (TS) or valine-to-serine (VS) substitution. Both variants caused developmental delays and lethality in both sexes and increase prevalence of deformities in females. Surprisingly, female TS and VS flies experienced increased lifespan and mistranslating males and females showed improved locomotion. These results suggest that mistranslation has both positive and negative effects that depend on the tRNA variant and sex of the fly.

genetics↗

Hsp90 and its co-chaperone Sti1 control TDP-43 misfolding and toxicity

Protein misfolding is a central feature of most neurodegenerative diseases. Molecular chaperones can modulate the toxicity associated with protein misfolding, but it remains elusive which molecular chaperones and co-chaperones interact with specific misfolded proteins. TDP-43 misfolding and inclusion formation is a hallmark of amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases. Using yeast and mammalian neuronal cells we find that Hsp90 and its co-chaperones have a strong capacity to alter TDP-43 misfolding, inclusion formation, aggregation, and cellular toxicity. Our data also demonstrate that impaired Hsp90 function sensitizes cells to TDP-43 toxicity. We further show that the co-chaperone Sti1 specifically interacts with and modulates TDP-43 toxicity in a dose-dependent manner. Our study thus uncovers a previously unrecognized tie between Hsp90, Sti1, TDP-43 misfolding, and its cellular toxicity.

cell biology↗