|
|
||||||||
Short Communication |
1 Radboud University Medical Centre Nijmegen, Nijmegen Centre for Molecular Life Sciences, Department of Medical Microbiology, PO Box 9101, 6500 HB Nijmegen, The Netherlands
2 Radboud University Nijmegen, Institute for Molecules and Materials, Laboratory of Biophysical Chemistry, University of Nijmegen, Toernooiveld 1, 6525 ED Nijmegen, The Netherlands
Correspondence
Willem J. G. Melchers
w.melchers{at}ncmls.ru.nl
The enterovirus oriR is composed of two helices, X and Y, anchored by a kissing (K) interaction. For proper oriR function, certain areas of these helices should be specifically oriented towards each other. It was hypothesized that the single-stranded nucleotides bridging the coaxial helices (YX and KY linkers) are important to determine this orientation. Spatial changes were introduced by altering the linker length between the helices of the coxsackievirus B3 oriR. Changing the linker lengths resulted in defective RNA replication, probably because of an altered oriR geometry. The identity of the linker residues also played a role, possibly because of sequence-specific ligand recognition. Although each point mutation altering the primary sequence of the YX spacer resulted in defective growth at 36 °C, the mutations had a wild-type phenotype at 39 °C, indicating a cold-sensitive phenotype. The results show that the intrinsic connection between oriR structure and function is fine-tuned by the spacing between the coaxial RNA helices.
A rotating version of Fig. 1(c) is available as supplementary material in JGV Online.
This article has been cited by other articles:
![]() |
E. Martinez-Salas, A. Pacheco, P. Serrano, and N. Fernandez New insights into internal ribosome entry site elements relevant for viral gene expression J. Gen. Virol., March 1, 2008; 89(3): 611 - 626. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Zoll, M. Tessari, F. J.M. Van Kuppeveld, W. J.G. Melchers, and H. A. Heus Breaking pseudo-twofold symmetry in the poliovirus 3'-UTR Y-stem by restoring Watson-Crick base pairs RNA, May 1, 2007; 13(5): 781 - 792. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Serrano, M. R. Pulido, M. Saiz, and E. Martinez-Salas The 3' end of the foot-and-mouth disease virus genome establishes two distinct long-range RNA-RNA interactions with the 5' end region. J. Gen. Virol., October 1, 2006; 87(Pt 10): 3013 - 3022. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Wessels, R. A. Notebaart, D. Duijsings, K. Lanke, B. Vergeer, W. J. G. Melchers, and F. J. M. van Kuppeveld Structure-Function Analysis of the Coxsackievirus Protein 3A: IDENTIFICATION OF RESIDUES IMPORTANT FOR DIMERIZATION, VIRAL RNA REPLICATION, AND TRANSPORT INHIBITION J. Biol. Chem., September 22, 2006; 281(38): 28232 - 28243. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| INT J SYST EVOL MICROBIOL | MICROBIOLOGY | J GEN VIROL |
| J MED MICROBIOL | ALL SGM JOURNALS | |