The universal Kae1 protein and the associated Bud32 kinase (PRPK), a mysterious protein couple probably essential for genome maintenance in Archaea and Eukarya. (20th January 2009)

• Record Type: Journal Article
• Authors: Hecker, Arnaud; Graille, Marc; Madec, Edwige; Gadelle, Danièle; Le Cam, Eric; van Tilbergh, Herman; Forterre, Patrick
• Is Part Of: Biochemical Society transactions. Volume 37:Number 1(2009)
• Page Start: 29
• Page End: 35
• Publication Date: 2009-01-20
• Subjects: Bud32 -- endopeptidase-like kinase chromatin-associated (EKC) -- kinase-associated endopeptidase 1 (Kae1) -- kinase -- endopeptidase and other proteins of small size (KEOPS) -- O-sialoglycoprotein endopeptidase (OSGEP) -- p53-related protein kinase (PRPK); Biochemistry -- Congresses; 572
• DOI: 10.1042/BST0370029
• Languages: English
• ISSNs: 0300-5127

Abstract

Abstract : The similarities between essential molecular mechanisms in Archaea and Eukarya make it possible to discover, using comparative genomics, new fundamental mechanisms conserved between these two domains. We are studying a complex of two proteins conserved in Archaea and Eukarya whose precise biological role and biochemical function remain unknown. One of them is a universal protein known as Kae1 (kinase-asociated endopeptidase 1). The second protein is a serine/threonine kinase corresponding to the proteins Bud32 in Saccharomyces cerevisiae and PRPK (p53-related protein kinase) in humans. The genes encoding the archaeal orthologues of Kae1 and PRPK are either contiguous or even fused in many archaeal genomes. In S. cerevisiae, Kae1 and Bud32 (PRPK) belong to a chromatin-associated complex [KEOPS (kinase, endopeptidase and other proteins of small size)/EKC (endopeptidase-like kinase chromatin-associated)] that is essential for telomere elongation and transcription of essential genes. Although Kae1 is annotated as O-sialoglycoprotein endopeptidase in most genomes, we found that the Kae1 protein from Pyrococcus abyssi has no protease activity, but is an atypical DNA-binding protein with an AP (apurinic) lyase activity. The structure of the fusion protein from Methanocaldococcus jannaschii revealed that Kae1 maintains the ATP-binding site of Kae1 in an inactive configuration. We have in fact found that Kae1 inhibits the kinase activity of Bud32 (PRPK) in vitro . Understanding the precise biochemical function and biological role of these two proteins (which are probably essential for genome maintenance) remains a major challenge.