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Disordered RNA chaperone proteins: from functions to disease
Authors:R. Ivanyi-Nagy  L. Davidovic  E. W. Khandjian  J.-L. Darlix
Affiliation:(1) Unité de Virologie Humaine (412), Ecole Normale Supérieure de Lyon et Institut National de la Santé et de la Recherche Médicale, IFR 128, 46 allée d’Italie, 69 364 Lyon, France;(2) Unité de Recherche en Génétique Humaine et Moléculaire, le CHUQ-Hôpital St-François d’Assise, Université Laval, Québec, G1L 3L5, Canada
Abstract:RNA chaperones are ubiquitous proteins that play pivotal roles in cellular RNA metabolism and RNA virus replication. Here we propose that they act by organizing complex and highly dynamic networks of RNA-RNA, RNA-protein and protein-protein interactions. How this is achieved and how their malfunction may lead to disease will be discussed through the examples of human immunodeficiency virus type 1 nucleocapsid protein (NCp7), the fragile X mental retardation protein and the prion protein.Received 9 March 2005; received after revision 6 April 2005; accepted 6 April 2005Dedicated to the memory of Dominique Dormont
Keywords:Intrinsically unstructured proteins  RNA-binding proteins  RNA chaperones  human immunodeficiency virus  NCp7  fragile X mental retardation  FMRP  prion diseases
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