Skip Navigation

This Article
Right arrow Full Text Freely available
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 ISI Web of Science
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 arrow Search for citing articles in:
ISI Web of Science (16)
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Hartshorne, T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hartshorne, T.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, Vol 26, Issue 11 2541-2553, Copyright © 1998 by Oxford University Press


ARTICLES

Distinct regions of U3 snoRNA interact at two sites within the 5' external transcribed spacer of pre-rRNAs in Trypanosoma brucei cells

T Hartshorne
Department of Biochemistry and Molecular Biology A-10, Albany Medical College, 47 New Scotland Avenue, Albany, NY 12208, USA. toinette_hartshorne@ccgateway.amc.edu

U3 snoRNA is required for early pre-rRNA processing events that include cleavage of the 5' external transcribed spacer (5'ETS) and 18S rRNA maturation. Herein, psoralen RNA crosslinking has been used to indicate novel in vivo interactions between the minimally-sized Trypanosoma brucei U3 snoRNA and pre-rRNAs. Two discrete U3 crosslinks were mapped to 5'ETS sequences, then individually isolated by hybrid selection following digestion of pre-rRNAs. Crosslink positions within these U3- site1 and U3-site2 complexes were resolved by RNaseH digestion and primer extension analyses. Hinge bases of U3 contacted site1 bases U140 and U142 just 3' of the processed primary site. This is the first experimental evidence of a U3 RNA interaction adjacent to a major 5'ETS cleavage site and supports a critical role for U3 in its processing. Highly conserved box A bases contacted site2 base U945, 187 nt upstream of 18S-like rRNA sequences. Site2 sequences are not required for primary processing, thus, a U3 interaction here might have roles in subsequent downstream processing events. These results clearly demonstrated that distinct U3 snoRNA sequences crosslinked different regions of the 5'ETS and support a model for U3 as a multifunctional snoRNA.
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
Eukaryot CellHome page
S. Barth, B. Shalem, A. Hury, I. D. Tkacz, X.-h. Liang, S. Uliel, I. Myslyuk, T. Doniger, M. Salmon-Divon, R. Unger, et al.
Elucidating the Role of C/D snoRNA in rRNA Processing and Modification in Trypanosoma brucei
Eukaryot. Cell, January 1, 2008; 7(1): 86 - 101.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
O. Fernandez-Miragall and E. Martinez-Salas
In vivo footprint of a picornavirus internal ribosome entry site reveals differences in accessibility to specific RNA structural elements
J. Gen. Virol., November 1, 2007; 88(11): 3053 - 3062.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
S. Barth, A. Hury, X.-h. Liang, and S. Michaeli
Elucidating the Role of H/ACA-like RNAs in trans-Splicing and rRNA Processing via RNA Interference Silencing of the Trypanosoma brucei CBF5 Pseudouridine Synthase
J. Biol. Chem., October 14, 2005; 280(41): 34558 - 34568.
[Abstract] [Full Text] [PDF]


Home page
RNAHome page
A. V. BOROVJAGIN and S. A. GERBI
Xenopus U3 snoRNA docks on pre-rRNA through a novel base-pairing interaction
RNA, June 1, 2004; 10(6): 942 - 953.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
A. Colley, J. D. Beggs, D. Tollervey, and D. L. J. Lafontaine
Dhr1p, a Putative DEAH-Box RNA Helicase, Is Associated with the Box C+D snoRNP U3
Mol. Cell. Biol., October 1, 2000; 20(19): 7238 - 7246.
[Abstract] [Full Text]


Home page
Nucleic Acids ResHome page
M. N. Schnare, J. C. Collings, D. F. Spencer, and M. W. Gray
The 28S-18S rDNA intergenic spacer from Crithidia fasciculata: repeated sequences, length heterogeneity, putative processing sites and potential interactions between U3 small nucleolar RNA and the ribosomal RNA precursor
Nucleic Acids Res., September 15, 2000; 28(18): 3452 - 3461.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
M. Antal, A. Mougin, M. Kis, E. Boros, G. Steger, G. Jakab, F. Solymosy, and C. Branlant
Molecular characterization at the RNA and gene levels of U3 snoRNA from a unicellular green alga, Chlamydomonas reinhardtii
Nucleic Acids Res., August 1, 2000; 28(15): 2959 - 2968.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
K. Sharma and D. Tollervey
Base Pairing between U3 Small Nucleolar RNA and the 5' End of 18S rRNA Is Required for Pre-rRNA Processing
Mol. Cell. Biol., September 1, 1999; 19(9): 6012 - 6019.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
D. A. Dunbar, S. Wormsley, T. M. Lowe, and S. J. Baserga
Fibrillarin-associated Box C/D Small Nucleolar RNAs in Trypanosoma brucei. SEQUENCE CONSERVATION AND IMPLICATIONS FOR 2'-O-RIBOSE METHYLATION OF rRNA
J. Biol. Chem., May 5, 2000; 275(19): 14767 - 14776.
[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.