Biology subjects

Garcia-Corzo, L.

Publications and source records attributed to Garcia-Corzo, L..

3 recordsLinked to original sources

bioRxiv2026

Prevalent phenotypic mutation impairs binding of broadly neutralizing antibodies to influenza hemagglutinin

Mistakes during protein synthesis, such as transcription errors, occur often and lead to non-inheritable amino acid replacements generally known as phenotypic mutations. We recently used a consensus approach in high-throughput sequencing to determine the error landscape for influenza-hemagglutinin mRNA. We found single-site errors to occur with widely different frequencies. Here we show that the most prevalent transcription error encodes a phenotypic mutation that impairs binding of broadly neutralizing antibodies. The error occurs in 0.2-0.5% of mRNA molecules and, consequently, many virions will expose hemagglutinin variants bearing the encoded amino acid replacement. Our results point to a mechanism of antibody evasion, akin to programmed recoding, in which evading mutations are encoded by transcription errors promoted by inheritable RNA sequence/structure patterns.

microbiology↗

bioRxiv2026

Influenza evolution/adaptation samples a highly non-random error landscape for hemagglutinin-encoding RNA

Natural selection acts on diversity generated by errors in the biosynthesis of the genetic material. Previous work has shown, however, that such errors are not necessarily fully random. We have used a model influenza strain and a unique-molecular-identifier-based high-throughput sequencing approach to assess the error landscape for hemagglutinin-encoding RNA. Single-site errors occur at highly variable frequencies, with differences that span several orders of magnitude, plausibly reflecting specific RNA sequence/structure patterns. Remarkably, influenza evolution/adaptation preferentially selects mutations encoded by the higher frequency errors, as shown by analyses of mutations fixed in natural strains over many decades and by analyses of antibody-escape mutations found in laboratory experiments on strains of the 2009 pandemics. Our results support that RNA error landscapes may provide information useful for predicting influenza evolution and point to high-frequency errors encoding antibody-evading mutations as potential contributors to the rapid evolution of influenza viruses.

microbiology↗

bioRxiv2023

COQ4 is required for the oxidative decarboxylation of the C1 carbon of Coenzyme Q in eukaryotic cells

Coenzyme Q (CoQ) is a redox lipid that fulfills critical functions in cellular bioenergetics and homeostasis. CoQ is synthesized by a multi-step pathway that involves several COQ proteins. Two steps of the eukaryotic pathway, the decarboxylation and hydroxylation of position C1, have remained uncharacterized. Here, we provide evidence that these two reactions occur in a single oxidative decarboxylation step catalyzed by COQ4. We demonstrate that COQ4 complements an Escherichia coli strain deficient for C1 decarboxylation and hydroxylation and that COQ4 displays oxidative decarboxylation activity in the non-CoQ producer Corynebacterium glutamicum. Overall, our results substantiate that COQ4 contributes to CoQ biosynthesis, not only via its previously proposed structural role, but also via oxidative decarboxylation of CoQ precursors. These findings fill a major gap in the knowledge of eukaryotic CoQ biosynthesis, and shed new light on the pathophysiology of human primary CoQ deficiency due to COQ4 mutations.

biochemistry↗