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A unique surface on Pat1 C-terminal domain directly interacts with Dcp2 decapping enzyme and Xrn1 5′–3′ mRNA exonuclease in yeast

  • Clément Charenton
  • , Claudine Gaudon-Plesse
  • , Zaineb Fourati
  • , Valerio Taverniti
  • , Régis Back
  • , Olga Kolesnikova
  • , Bertrand Séraphin
  • , Marc Graille
  • Institut Polytechnique de Paris
  • Institut de Génétique et de Biologie Moléculaire et Cellulaire
  • Université de Strasbourg

Résultats de recherche: Contribution à un journal › Article › Revue par des pairs

38 Citations (Scopus)

Résumé

The Pat1 protein is a central player of eukaryotic mRNA decay that has also been implicated in translational control. It is commonly considered a central platform responsible for the recruitment of several RNA decay factors. We demonstrate here that a yeast-specific C-terminal region from Pat1 interacts with several short motifs, named helical leucine-rich motifs (HLMs), spread in the long C-terminal region of yeast Dcp2 decapping enzyme. Structures of Pat1–HLM complexes reveal the basis for HLM recognition by Pat1. We also identify a HLM present in yeast Xrn1, the main 5′–3′ exonuclease involved in mRNA decay. We show further that the ability of yeast Pat1 to bind HLMs is required for efficient growth and normal mRNA decay. Overall, our analyses indicate that yeast Pat1 uses a single binding surface to successively recruit several mRNA decay factors and show that interaction between those factors is highly polymorphic between species.

langue originaleAnglais
Pages (de - à)E9493-E9501
journalProceedings of the National Academy of Sciences of the United States of America
Volume114
Numéro de publication45
Les DOIs
étatPublié - 7 nov. 2017

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