Literature DB >> 10471494

A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation.

A Carrié1, L Jun, T Bienvenu, M C Vinet, N McDonell, P Couvert, R Zemni, A Cardona, G Van Buggenhout, S Frints, B Hamel, C Moraine, H H Ropers, T Strom, G R Howell, A Whittaker, M T Ross, A Kahn, J P Fryns, C Beldjord, P Marynen, J Chelly.   

Abstract

We demonstrate here the importance of interleukin signalling pathways in cognitive function and the normal physiology of the CNS. Thorough investigation of an MRX critical region in Xp22.1-21.3 enabled us to identify a new gene expressed in brain that is responsible for a non-specific form of X-linked mental retardation. This gene encodes a 696 amino acid protein that has homology to IL-1 receptor accessory proteins. Non-overlapping deletions and a nonsense mutation in this gene were identified in patients with cognitive impairment only. Its high level of expression in post-natal brain structures involved in the hippocampal memory system suggests a specialized role for this new gene in the physiological processes underlying memory and learning abilities.

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Year:  1999        PMID: 10471494     DOI: 10.1038/12623

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  52 in total

Review 1.  Genetic effects on human cognition: lessons from the study of mental retardation syndromes.

Authors:  P Nokelainen; J Flint
Journal:  J Neurol Neurosurg Psychiatry       Date:  2002-03       Impact factor: 10.154

2.  IL1RAPL1 gene deletion as a cause of X-linked intellectual disability and dysmorphic features.

Authors:  Erin L Youngs; Rebecca Henkhaus; Jessica A Hellings; Merlin G Butler
Journal:  Eur J Med Genet       Date:  2011-09-10       Impact factor: 2.708

3.  Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneity.

Authors:  L Basel-Vanagaite; A Alkelai; R Straussberg; N Magal; D Inbar; M Mahajna; M Shohat
Journal:  J Med Genet       Date:  2003-10       Impact factor: 6.318

4.  Molecular and clinical characterization of a small duplication Xp in a human female with psychiatric disorders.

Authors:  Maria Piccione; Cinzia Sanfilippo; Simona Cavani; Patrizia Salatiello; Michela Malacarne; Mauro Pierluigi; Marco Fichera; Daniela Luciano; Giovanni Corsello
Journal:  J Genet       Date:  2011-12       Impact factor: 1.166

Review 5.  X linked mental retardation: a clinical guide.

Authors:  F L Raymond
Journal:  J Med Genet       Date:  2005-08-23       Impact factor: 6.318

Review 6.  Protein tyrosine phosphatases PTPδ, PTPσ, and LAR: presynaptic hubs for synapse organization.

Authors:  Hideto Takahashi; Ann Marie Craig
Journal:  Trends Neurosci       Date:  2013-07-05       Impact factor: 13.837

Review 7.  The expanding interleukin-1 family and its receptors: do alternative IL-1 receptor/signaling pathways exist in the brain?

Authors:  Herve Boutin; Ian Kimber; Nancy J Rothwell; Emmanuel Pinteaux
Journal:  Mol Neurobiol       Date:  2003-06       Impact factor: 5.590

8.  The effect of interleukin-1 blockade on fatigue in rheumatoid arthritis--a pilot study.

Authors:  Roald Omdal; Ragnar Gunnarsson
Journal:  Rheumatol Int       Date:  2004-04-08       Impact factor: 2.631

9.  Structural and functional deficits in a neuronal calcium sensor-1 mutant identified in a case of autistic spectrum disorder.

Authors:  Mark T W Handley; Lu-Yun Lian; Lee P Haynes; Robert D Burgoyne
Journal:  PLoS One       Date:  2010-05-07       Impact factor: 3.240

10.  Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions.

Authors:  Matteo Fumagalli; Uberto Pozzoli; Rachele Cagliani; Giacomo P Comi; Stefania Riva; Mario Clerici; Nereo Bresolin; Manuela Sironi
Journal:  J Exp Med       Date:  2009-05-25       Impact factor: 14.307

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