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Multiple snoRNA gene clusters from Arabidopsis

Published online by Cambridge University Press:  11 January 2002

JOHN W.S. BROWN
Affiliation:
Unit of Gene Expression, Genetics Division, Scottish Crop Research Institute, Invergowrie, Dundee DD2 5DA, Scotland, United Kingdom
GILLIAN P. CLARK
Affiliation:
Unit of Gene Expression, Genetics Division, Scottish Crop Research Institute, Invergowrie, Dundee DD2 5DA, Scotland, United Kingdom
DAVID J. LEADER
Affiliation:
Unit of Gene Expression, Genetics Division, Scottish Crop Research Institute, Invergowrie, Dundee DD2 5DA, Scotland, United Kingdom Present address: Syngenta, Norwich Research Park, Colney, Norwich NR4 7UH, United Kingdom.
CRAIG G. SIMPSON
Affiliation:
Unit of Gene Expression, Genetics Division, Scottish Crop Research Institute, Invergowrie, Dundee DD2 5DA, Scotland, United Kingdom
TODD LOWE
Affiliation:
Department of Computer Engineering, University of California, Santa Cruz, California 95064, USA
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Abstract

Small nucleolar RNAs (snoRNAs) are involved in precursor ribosomal RNA (pre-rRNA) processing and rRNA base modification (2′-O-ribose methylation and pseudouridylation). In all eukaryotes, certain snoRNAs (e.g., U3) are transcribed from classical promoters. In vertebrates, the majority are encoded in introns of protein-coding genes, and are released by exonucleolytic cleavage of linearized intron lariats. In contrast, in maize and yeast, nonintronic snoRNA gene clusters are transcribed as polycistronic pre-snoRNA transcripts from which individual snoRNAs are processed. In this article, 43 clusters of snoRNA genes, an intronic snoRNA, and 10 single genes have been identified by cloning and by computer searches, giving a total of 136 snoRNA gene copies of 71 different snoRNA genes. Of these, 31 represent snoRNA genes novel to plants. A cluster of four U14 snoRNA genes and two clusters containing five different snoRNA genes (U31, snoR4, U33, U51, and snoR5) from Arabidopsis have been isolated and characterized. Of these genes, snoR4 is a novel box C/D snoRNA that has the potential to base pair with the 3′ end of 5.8S rRNA and snoR5 is a box H/ACA snoRNA gene. In addition, 42 putative sites of 2′-O-ribose methylation in plant 5.8S, 18S, and 25S rRNAs have been mapped by primer extension analysis, including eight sites novel to plant rRNAs. The results clearly show that, in plants, the most common gene organization is polycistronic and that over a third of predicted and mapped methylation sites are novel to plant rRNAs. The variation in this organization among gene clusters highlights mechanisms of snoRNA evolution.

Type
Research Article
Information
RNA , Volume 7 , Issue 12 , December 2001 , pp. 1817 - 1832
Copyright
2001 RNA Society

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