Nucleic Acids Research, Vol 26, Issue 7 1775-1783, Copyright © 1998 by Oxford University Press
A Levitan, Yx Xu, C Ben-Dov, H Ben-Shlomo, Y Zhang and S Michaeli
Trypanosomes possess unique RNA processing mechanisms including trans-
splicing of pre-mRNA and RNA editing of mitochondrial transcripts. The
previous finding of a trimethylguanosine (TMG) capped U3 homologue in
trypanosomes suggests that rRNA processing may be related to the processing
in other eukaryotes. In this study, we describe the first trypanosomatid
snoRNA that belongs to the snoRNAs that were shown to guide ribose
methylation of rRNA. The RNA, identified in the monogenetic trypanosomatid
Leptomonas collosoma, was termed snoRNA-2 and is encoded by a multi-copy
gene. SnoRNA-2 is 85 nt long, it lacks a 5' cap and possesses the C and D
boxes characteristic to all snoRNAs that bind fibrillarin. Computer
analysis indicates a potential for base- pairing between snoRNA-2 and 5.8S
rRNA, and 18S rRNA. The putative interaction domains obey the rules
suggested for the interaction of guide snoRNA with its rRNA target for
directing ribose methylation on the rRNA. However, mapping the methylated
sites on the 5.8S rRNA and 18S rRNA indicates that the expected site on the
5.8S is methylated, whereas the site on the 18S is not. The proposed
interaction with 5.8S rRNA is further supported by the presence of psoralen
cross-link sites on snoRNA-2. GenBank search suggests that snoRNA-2 is not
related to any published snoRNAs. Because of the early divergence of the
Trypanosomatidae from the eukaryotic lineage, the presence of a methylating
snoRNA that is encoded by a multi-copy gene suggests that methylating
snoRNAs may have evolved in evolution from self-transcribed genes.
ARTICLES
Characterization of a novel trypanosomatid small nucleolar RNA
Department of Biological Chemistry, The Weizmann Institute of Science, Rehovot 76100, Israel.
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