Evolutionary and functional insights into the Ski2-like helicase family in Archaea: a comparison of Thermococcales ASH-Ski2 and Hel308 activities

Author:

Batista Manon1,Langendijk-Genevaux Petra2,Kwapisz Marta1,Canal Isabelle1,Phung Duy Khanh1,Plassart Laura1,Capeyrou Régine1,Moalic Yann3,Jebbar Mohamed3,Flament Didier3,Fichant Gwennaele2,Bouvier Marie1,Clouet-d’Orval Béatrice1ORCID

Affiliation:

1. MCD, Centre de Biologie Intégrative (CBI), CNRS, Université de Toulouse , UT3, Toulouse, France

2. LMGM, Centre de Biologie Intégrative (CBI), CNRS, Université de Toulouse , UT3, Toulouse, France

3. Univ Brest, CNRS, Ifremer, UMR6197 Biologie et Ecologie des Ecosystèmes marins Profonds , F-29280 Plouzané, France

Abstract

Abstract RNA helicases perform essential housekeeping and regulatory functions in all domains of life by binding and unwinding RNA molecules. The Ski2-like proteins are primordial helicases that play an active role in eukaryotic RNA homeostasis pathways, with multiple homologs having specialized functions. The significance of the expansion and diversity of Ski2-like proteins in Archaea, the third domain of life, has not yet been established. Here, by studying the phylogenetic diversity of Ski2-like helicases among archaeal genomes and the enzymatic activities of those in Thermococcales, we provide further evidence of the function of this protein family in archaeal metabolism of nucleic acids. We show that, in the course of evolution, ASH-Ski2 and Hel308-Ski2, the two main groups of Ski2-like proteins, have diverged in their biological functions. Whereas Hel308 has been shown to mainly act on DNA, we show that ASH-Ski2, previously described to be associated with the 5′-3′ aRNase J exonuclease, acts on RNA by supporting an efficient annealing activity, but also an RNA unwinding with a 3′-5′ polarity. To gain insights into the function of Ski2, we also analyse the transcriptome of Thermococcus barophilus ΔASH-Ski2 mutant strain and provide evidence of the importance of ASH-Ski2 in cellular metabolism pathways related to translation.

Funder

Agence Nationale pour la Recherche

Publisher

Oxford University Press (OUP)

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