Three Small Nucleolar RNAs Identified from the Spliced Leader-Associated RNA Locus in Kinetoplastid Protozoans

Author:

Roberts T. Guy1,Sturm Nancy R.1,Yee Billy K.1,Yu Michael C.1,Hartshorne Toinette2,Agabian Nina3,Campbell David A.1

Affiliation:

1. Department of Microbiology and Immunology, UCLA School of Medicine, Los Angeles, California 90095-1747 1 ;

2. Biochemistry & Molecular Biology, Albany Medical College, Albany, New York 12208 2 ; and

3. Program in Molecular Pathogenesis, University of California, San Francisco, California 94143-04223

Abstract

ABSTRACT First characterized in Trypanosoma brucei , the spliced leader-associated (SLA) RNA gene locus has now been isolated from the kinetoplastids Leishmania tarentolae and Trypanosoma cruzi . In addition to the T. brucei SLA RNA, both L. tarentolae and T. cruzi SLA RNA repeat units also yield RNAs of 75 or 76 nucleotides (nt), 92 or 94 nt, and ∼450 or ∼350 nt, respectively, each with significant sequence identity to transcripts previously described from the T. brucei SLA RNA locus. Cell fractionation studies localize the three additional RNAs to the nucleolus; the presence of box C/D-like elements in two of the transcripts suggests that they are members of a class of small nucleolar RNAs (snoRNAs) that guide modification and cleavage of rRNAs. Candidate rRNA-snoRNA interactions can be found for one domain in each of the C/D element-containing RNAs. The putative target site for the 75/76-nt RNA is a highly conserved portion of the small subunit rRNA that contains 2′- O -ribose methylation at a conserved position (Gm1830) in L. tarentolae and in vertebrates. The 92/94-nt RNA has the potential to form base pairs near a conserved methylation site in the large subunit rRNA, which corresponds to position Gm4141 of small rRNA 2 in T. brucei . These data suggest that trypanosomatids do not obey the general 5-bp rule for snoRNA-mediated methylation.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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