Pat1 globally activates deadenylation-dependent decapping to clear inefficiently translated oligo(A)-tailed transcripts
Lucie Labeauvie, Jackson Peter, Hélène Zuber, Bertrand Séraphin
bioRxiv · Oct 23, 2026 · PreprintMolecular Biology
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Centre National de la Recherche ScientifiqueORCID 0000-0002-4094-5258Unclaimed ORCID profile · follow to get notified of new preprints
6 papers
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Lucie Labeauvie, Jackson Peter, Hélène Zuber, Bertrand Séraphin
bioRxiv · Oct 23, 2026 · PreprintMolecular Biology
Jackson Peter, Jeanne Roignant, Sebastian Sacharowski, Élodie Ubrig, Benjamin Lefèvre, Szymon Świeżewski, Dominique Gagliardi, Hélène Zuber
This study identifies URT1 as the main enzyme for mRNA uridylation in Arabidopsis, showing its role in shaping the seed transcriptome and regulating primary dormancy.
The Plant Cell · Feb 1, 2026Peer-reviewedPlant Biology
Philippe Johann to Berens, Jackson Peter, Sandrine Koechler, Mathieu Bruggeman, Sébastien Staerck, Jean Molinier
This study identifies JMJ27 as a histone demethylase that modulates H3K9me2 levels during UV-induced photodamage repair in plants.
Nature Plants · Oct 4, 2024Peer-reviewedPlant Biology
Téo Fournier, Omar Abou Saada, Jing Hou, Jackson Peter, Élodie Caudal, Joseph Schacherer
The paper shows low-frequency genetic variants contribute significantly to phenotypic variation in a yeast population using a diallel cross experiment and GWAS.
eLife · Oct 24, 2019Peer-reviewedGenomics
Christian Brion, Sylvain Legrand, Jackson Peter, Claudia Caradec, David Pflieger, Jing Hou, Anne Friedrich, Bertrand Llorente, Joseph Schacherer
The paper examines meiotic recombination differences between Saccharomyces cerevisiae and Lachancea kluyveri, finding significant variations in recombination rates, crossover patterns, and hotspot conservation across evolutionary distances.
PLoS Genetics · Aug 1, 2017Peer-reviewedGenomics
Jing Hou, Anastasie Sigwalt, David Pflieger, Jackson Peter, Jacky de Montigny, Maitreya Dunham, Joseph Schacherer
The paper investigates Mendelian traits in yeast, finding that most are caused by common variants with stable inheritance, while a rare variant shows complex, context-dependent expression.
bioRxiv · Feb 15, 2016Genomics