Département de Biochimie, Université de Montréal, Montréal, Québec, Canada H3C 3J7
§ Present address: Cold Spring Harbor Laboratory, Cold Spring Harbor, New York, USA 11724
¶ To whom correspondence should be addressed.Tel: (514) 343-1938, fax: (514) 343-2210, E-mail: paquinb@magellan.umontreal.ca
*Dedicated to the late Robert Cedergren.
Nucleic Acids Res. 27: 4457-4467.(2000)
ABSTRACT
Functional analysis of genome sequences has largely ignored RNA genes
and their structures. We introduce here the notion of "ribonomics" to describe
the search for the distribution of and eventually the determination of the
physiological roles of these RNA structures found in the sequence databases. The
utility of this approach is illustrated here by the identification in the
GenBank database of RNA motifs having known binding or chemical activity. The
frequency of these motifs indicates that most have originated from evolutionary
drift and are selectively neutral. On the other hand, their distribution among
species and their location within genes suggest that the destiny of these motifs
may be more elaborate. For example, the hammerhead motif has a skewed organismal
presence, is phylogenetically stable and recent work on a schistosome version
confirms its in vivo biological activity. The under representation of the
valine-binding motif and the Rev- binding element in Genbank hints at a
detrimental effect on cell growth or viability. Data on the presence and the
location of these motifs may provide critical guidance in the design of
experiments directed towards the understanding and the manipulation of RNA
complexes and activities in vivo.
KeyWords: RNA motifs, database search, ribonomics, RNA-binding proteins,
catalytic RNAs.
The abstract and the figures have been reproduced with the permission of Oxford University Press (http://www.nar.oupjournals.org).
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Last modified 09-23-99
Véronique Bourdeau, Marie Pageau - Copyright ©1999