Substrate Requirements for a Novel Archaeal Endonuclease That Cleaves Within the 5' External Transcribed Spacer of Sulfolobus acidocaldarius Precursor rRNA

Corresponding author: Patrick P. Dennis, Department of Biochemistry and Molecular Biology, University of British Columbia, 2146 Health Sciences Mall, Vancouver, BC V6T 1Z3, Canada., patrickp.dennis{at}ubc.ca (E-mail)

Communicating editor: P. BLUM

During ribosome biogenesis in the hyperthermophilic archaeon Sulfolobus acidocaldarius, at least three separate precursor endonucleolytic cleavages occur within the 144-nucleotide-long 5' external transcribed spacer (5' ETS) region of the rRNA operon primary transcript. The 5' ETS sequence contains three regions of very stable helical structure. One cleavage (5' to position -98) is in the single-stranded region between the 5' and the central helical domains; a second cleavage (5' to position -31) is in the single-stranded region between the central and the 3' helical domains; and a third cleavage is at the 5' ETS-16S junction (5' to position +1). The three sites share a common consensus sequence around the position of cleavage. We have used an in vitro pre-RNA processing assay to define some of the sequence and structural recognition elements necessary for the two precursor cleavages 5' to positions -98 and -31. Surprisingly, none of the three predominant helical domains are required for recognition or targeting of the cleavages, although their removal reduces the rate of cleavage site utilization. We show that the sequence AAG (CA)UU encompassing each site contains at least some of the essential features for recognition and efficient targeting of the cleavages. Cleavage depends on the presence of a purine 5' and a uracil two nucleotides 3' to the scissile phosphodiester bond. Mutations to other bases at these critical positions are either not cleaved or cleaved very poorly. Finally, on the basis of intermediates that are produced during a processing reaction, we can conclude that the cleavages at positions 98 and 31 are not ordered in vitro.

This article has been cited by other articles:

				S. Hundt, A. Zaigler, C. Lange, J. Soppa, and G. Klug Global Analysis of mRNA Decay in Halobacterium salinarum NRC-1 at Single-Gene Resolution Using DNA Microarrays J. Bacteriol., October 1, 2007; 189(19): 6936 - 6944. [Abstract] [Full Text] [PDF]

				A. Jager, R. Samorski, F. Pfeifer, and G. Klug Individual gvp transcript segments in Haloferax mediterranei exhibit varying half-lives, which are differentially affected by salt concentration and growth phase Nucleic Acids Res., December 15, 2002; 30(24): 5436 - 5443. [Abstract] [Full Text] [PDF]

				T. H. Tang, T. S. Rozhdestvensky, B. C. d'Orval, M.-L. Bortolin, H. Huber, B. Charpentier, C. Branlant, J.-P. Bachellerie, J. Brosius, and A. Huttenhofer RNomics in Archaea reveals a further link between splicing of archaeal introns and rRNA processing Nucleic Acids Res., February 15, 2002; 30(4): 921 - 930. [Abstract] [Full Text] [PDF]

				A. Ciammaruconi and P. Londei In Vitro Processing of the 16S rRNA of the Thermophilic Archaeon Sulfolobus solfataricus J. Bacteriol., July 1, 2001; 183(13): 3866 - 3874. [Abstract] [Full Text] [PDF]

				W. B. Whitman, F. Pfeifer, P. Blum, and A. Klein What Archaea Have to Tell Biologists Genetics, August 1, 1999; 152(4): 1245 - 1248. [Full Text]