Abstract

BackgroundSmall nucleolar RNAs (snoRNAs) are a large group of non-coding RNAs (ncRNAs) that mainly guide 2'-O-methylation (C/D RNAs) and pseudouridylation (H/ACA RNAs) of ribosomal RNAs. The pattern of rRNA modifications and the set of snoRNAs that guide these modifications are conserved in vertebrates. Nearly all snoRNA genes in vertebrates are localized in introns of other genes and are processed from pre-mRNAs. Thus, the same promoter is used for the transcription of snoRNAs and host genes.ResultsThe series of studies by Dahai Zhu and coworkers on snoRNAs and their genes were critically considered. We present evidence that dozens of species-specific snoRNAs that they described in vertebrates are experimental artifacts resulting from the improper use of Northern hybridization. The snoRNA genes with putative intrinsic promoters that were supposed to be transcribed independently proved to contain numerous substitutions and are, most likely, pseudogenes. In some cases, they are localized within introns of overlooked host genes. Finally, an increased number of snoRNA genes in mammalian genomes described by Zhu and coworkers is also an artifact resulting from two mistakes. First, numerous mammalian snoRNA pseudogenes were considered as genes, whereas most of them are localized outside of host genes and contain substitutions that question their functionality. Second, Zhu and coworkers failed to identify many snoRNA genes in non-mammalian species. As an illustration, we present 1352 C/D snoRNA genes that we have identified and annotated in vertebrates.ConclusionsOur results demonstrate that conclusions based only on databases with automatically annotated ncRNAs can be erroneous. Special investigations aimed to distinguish true RNA genes from their pseudogenes should be done. Zhu and coworkers, as well as most other groups studying vertebrate snoRNAs, give new names to newly described homologs of human snoRNAs, which significantly complicates comparison between different species. It seems necessary to develop a uniform nomenclature for homologs of human snoRNAs in other vertebrates, e.g., human gene names prefixed with several-letter code denoting the vertebrate species.

Highlights

  • Small nucleolar RNAs are a large group of non-coding RNAs that mainly guide 2’-O-methylation (C/D RNAs) and pseudouridylation (H/ACA RNAs) of ribosomal RNAs

  • We have demonstrated that the set of C/D snoRNAs is well conserved among vertebrates and that species-specific snoRNAs guiding rRNA modifications are extremely rare

  • All of them were homologs of known human snoRNAs. Expression of these RNAs was tested by Northern hybridization in the muscle of several vertebrate species

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Summary

Introduction

Small nucleolar RNAs (snoRNAs) are a large group of non-coding RNAs (ncRNAs) that mainly guide 2’-O-methylation (C/D RNAs) and pseudouridylation (H/ACA RNAs) of ribosomal RNAs. The pattern of rRNA modifications and the set of snoRNAs that guide these modifications are conserved in vertebrates. Small nucleolar RNAs constitute one of the largest groups of ncRNAs. They guide 2’-O-methylation and pseudouridylation of target RNAs, mainly rRNAs. SnoRNAs are divided into two groups according to the modification type: C/D box snoRNAs guide 2’-O-methylation, while H/ACA box snoRNAs guide pseudouridylation [1,2]. C/D box snoRNAs contain conserved C (UGAUGA) and D (CUGA) boxes brought together by complementary interactions between the snoRNA termini [4].

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