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Review
, 20 (14), 3617-22

Small Nucleolar RNA-guided Post-Transcriptional Modification of Cellular RNAs

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Review

Small Nucleolar RNA-guided Post-Transcriptional Modification of Cellular RNAs

T Kiss. EMBO J.

Figures

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Fig. 1. Structure and function of (A) 2′-O-methylation and (B) pseudouridylation guide snoRNAs. The consensus sequences of boxes C, C′, D, D′, H and ACA are indicated (R is a purine and N stands for any nucleotide). Models for molecular selection of 2′-O-methylated nucleotides and pseudouridine were adopted from Kiss-László et al. (1998) and Ganot et al. (1997a), respectively.
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Fig. 2. Biogenesis and function of 2′-O-methylation and pseudouridylation guide snoRNAs. In mammalian cells, all guide RNAs are synthesized within introns of pre-mRNAs in the nucleoplasm. Most intronic snoRNAs are processed from the removed and debranched host intron by exonucleolytic activities. It remains unclear whether 5′ and 3′ end processing of snoRNAs occurs already in the nucleoplasm, or later in the nucleolus. Guide snoRNAs accumulating in the nucleolus direct 2′-O-methylation and pseudouridylation of the 18S, 5.8S and 28S rRNAs, the U6 snRNA and perhaps other cellular RNAs, including tRNAs, the signal recognition particle (SRP) and telomerase RNAs. It seems that box C/D, but not box H/ACA snoRNAs, transiently appear in the Cajal body before accumulating in the nucleolus. Some guide RNAs (scaRNAs) directing modification of the pol II-transcribed spliceosomal snRNAs accumulate in the Cajal body (CB). For other details, see the text.

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