Prp43/DHX15 exemplify RNA helicase multifunctionality in the gene expression network

Author:

Bohnsack Katherine E1ORCID,Kanwal Nidhi1,Bohnsack Markus T12ORCID

Affiliation:

1. Department of Molecular Biology, University Medical Center Göttingen , Humboldtallee 23 , 37073 Göttingen , Germany

2. Göttingen Center for Molecular Biosciences, Georg August University of Göttingen , Justus-von-Liebig-Weg 11 , 37077 Göttingen , Germany

Abstract

Abstract Dynamic regulation of RNA folding and structure is critical for the biogenesis and function of RNAs and ribonucleoprotein (RNP) complexes. Through their nucleotide triphosphate-dependent remodelling functions, RNA helicases are key modulators of RNA/RNP structure. While some RNA helicases are dedicated to a specific target RNA, others are multifunctional and engage numerous substrate RNAs in different aspects of RNA metabolism. The discovery of such multitasking RNA helicases raises the intriguing question of how these enzymes can act on diverse RNAs but also maintain specificity for their particular targets within the RNA-dense cellular environment. Furthermore, the identification of RNA helicases that sit at the nexus between different aspects of RNA metabolism raises the possibility that they mediate cross-regulation of different cellular processes. Prominent and extensively characterized multifunctional DEAH/RHA-box RNA helicases are DHX15 and its Saccharomyces cerevisiae (yeast) homologue Prp43. Due to their central roles in key cellular processes, these enzymes have also served as prototypes for mechanistic studies elucidating the mode of action of this type of enzyme. Here, we summarize the current knowledge on the structure, regulation and cellular functions of Prp43/DHX15, and discuss the general concept and implications of RNA helicase multifunctionality.

Funder

Deutsche Forschungsgemeinschaft

Universitätsmedizin Göttingen

Publisher

Oxford University Press (OUP)

Subject

Genetics

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