Skip Navigation

This Article
Right arrow Print PDF (3233K)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Prislei, S.
Right arrow Articles by Bozzoni, I.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Prislei, S.
Right arrow Articles by Bozzoni, I.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1993, Vol. 21, No. 25 5824-5830
© 1993


RNA

Two different snoRNAs are encoded in introns of amphibian and human L1 ribosomal protein genes

Silvia Prislei, Alessandro Michienzi, Carlo Presutti, Paola Fragapane1 and Irene Bozzoni*

Istituto Pasteur Fondazione Cenci-Bolognetti 1Centro Acidi Nucleici of CNR, Dipartimento di Genetica e Biologia Molecolare, Universita` 'La Sapienza', Rome, Italy

To whom correspondence should be addressed

Received October 20, 1993. Revised November 16, 1993. Accepted November 16, 1993.

We previously reported that the third intron of the X.laevis L1 ribosomal protein gene encodes for a snoRNA called U16. Here we show that four different introns of the same gene contain another previously uncharacterized snoRNA (U18) which is associated with fibrillarin in the nucleolus and which originates by processing of the pre-mRNA. The pathway of U18 RNA release from the pre-mRNA is the same as the one described for U16: primary endonucleolytic cleavages upstream and downstream of the U18 coding region produce a pre-U18 RNA which is subsequently trimmed to the mature form. Both the gene organization and processing of U18 are conserved in the corresponding genes of X.tropicalis and H.sapiens. The L1 gene thus has a composite structure, highly conserved in evolution, in which sequences coding for a ribosomal protein are intermingled with sequences coding for two different snoRNAs. The nucleolar localization of these different components suggests some common function on ribosome biosynthesis.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Mol Biol EvolHome page
J. S. Mattick and M. J. Gagen
Review ArticleThe Evolution of Controlled Multitasked Gene Networks: The Role of Introns and Other Noncoding RNAs in the Development of Complex Organisms
Mol. Biol. Evol., September 1, 2001; 18(9): 1611 - 1630.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
X. Darzacq and T. Kiss
Processing of Intron-Encoded Box C/D Small Nucleolar RNAs Lacking a 5',3'-Terminal Stem Structure
Mol. Cell. Biol., July 1, 2000; 20(13): 4522 - 4531.
[Abstract] [Full Text]


Home page
Mol. Cell. Biol.Home page
T. Villa, F. Ceradini, and I. Bozzoni
Identification of a Novel Element Required for Processing of Intron-Encoded Box C/D Small Nucleolar RNAs in Saccharomyces cerevisiae
Mol. Cell. Biol., February 15, 2000; 20(4): 1311 - 1320.
[Abstract] [Full Text]


Home page
Mol. Cell. Biol.Home page
C. M. Smith and J. A. Steitz
Classification of gas5 as a Multi-Small-Nucleolar-RNA (snoRNA) Host Gene and a Member of the 5'-Terminal Oligopyrimidine Gene Family Reveals Common Features of snoRNA Host Genes
Mol. Cell. Biol., December 1, 1998; 18(12): 6897 - 6909.
[Abstract] [Full Text]


Home page
Mol. Cell. Biol.Home page
T. Villa, F. Ceradini, C. Presutti, and I. Bozzoni
Processing of the Intron-Encoded U18 Small Nucleolar RNA in the Yeast Saccharomyces cerevisiae Relies on Both Exo- and Endonucleolytic Activities
Mol. Cell. Biol., June 1, 1998; 18(6): 3376 - 3383.
[Abstract] [Full Text]


Home page
Mol. Cell. Biol.Home page
E. Petfalski, T. Dandekar, Y. Henry, and D. Tollervey
Processing of the Precursors to Small Nucleolar RNAs and rRNAs Requires Common Components
Mol. Cell. Biol., March 1, 1998; 18(3): 1181 - 1189.
[Abstract] [Full Text]


Home page
Mol. Cell. Biol.Home page
E. Caffarelli, M. Losito, C. Giorgi, A. Fatica, and I. Bozzoni
In Vivo Identification of Nuclear Factors Interacting with the Conserved Elements of Box C/D Small Nucleolar RNAs
Mol. Cell. Biol., February 1, 1998; 18(2): 1023 - 1028.
[Abstract] [Full Text]


Home page
Genome ResHome page
C Crosio, F Cecconi, P Mariottini, G Cesareni, S Brenner, and F Amaldi
Fugu intron oversize reveals the presence of U15 snoRNA coding sequences in some introns of the ribosomal protein S3 gene.
Genome Res., December 1, 1996; 6(12): 1227 - 1231.
[Abstract] [PDF]


Home page
Genes Dev.Home page
T Kiss and W Filipowicz
Exonucleolytic processing of small nucleolar RNAs from pre-mRNA introns.
Genes & Dev., June 1, 1995; 9(11): 1411 - 1424.
[Abstract] [PDF]


Home page
Genes Dev.Home page
E S Tasheva and D J Roufa
Regulation of human RPS14 transcription by intronic antisense RNAs and ribosomal protein S14.
Genes & Dev., February 1, 1995; 9(3): 304 - 316.
[Abstract] [PDF]


Home page
Genes Dev.Home page
B A Peculis and J A Steitz
Sequence and structural elements critical for U8 snRNP function in Xenopus oocytes are evolutionarily conserved.
Genes & Dev., September 15, 1994; 8(18): 2241 - 2255.
[Abstract] [PDF]


Home page
J. Biol. Chem.Home page
F. Barneche, F. Steinmetz, and M. Echeverria
Fibrillarin Genes Encode Both a Conserved Nucleolar Protein and a Novel Small Nucleolar RNA Involved in Ribosomal RNA Methylation in Arabidopsis thaliana
J. Biol. Chem., August 25, 2000; 275(35): 27212 - 27220.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.