Human Molecular Genetics, 2003, Vol. 12, No. 12 1415-1425
DOI: 10.1093/hmg/ddg147
© 2003 Oxford University Press
IL1 receptor accessory protein like, a protein involved in X-linked mental retardation, interacts with Neuronal Calcium Sensor-1 and regulates exocytosis
1Institut Cochin, INSERM Unité 567, CNRS UMR 8104, Université Paris V, CHU Cochin, 24 rue du Faubourg Saint Jacques, 75 014 Paris, France and 2The Physiological Laboratory, University of Liverpool, Crown Street, Liverpool L69 3BX, UK
Received January 20, 2003; Accepted April 4, 2003
Previously, human genetics-based approaches allowed us to show that mutations in the IL-1 receptor accessory protein-like gene (IL1RAPL) are responsible for a non-specific form of X-linked mental retardation. This gene encodes a predicted protein of 696 amino acids that belongs to a novel class of the IL-1/Toll receptor family. In addition to the extracellular portion consisting of three Ig-like domains and the intracellular TIR domain characteristic of the IL-1/Toll receptor family, IL1RAPL contains a specific 150 amino acid carboxy terminus that has no significant homology with any protein of known function. In order to begin to elucidate the function of this IL-1/Toll receptor-like protein, we have assessed the effect of recombinant IL1RAPL on the binding affinity of type I IL-1R for its ligands IL-1
and ß and searched for proteins interacting with the specific carboxy terminus domain of IL1RAPL. Our results show that IL1RAPL is not a protein receptor for IL-1. In addition we present here the identification of Neuronal Calcium Sensor-1 (NCS-1) as an IL1RAPL interactor. Remarkably, although NCS-1 and its non-mammalian homologue, frequenin, are members of a highly conserved EF-hand Ca2+ binding protein family, our data show that IL1RAPL interacts only with NCS-1 through its specific C-terminal domain. The functional relevance of IL1RAPL activity was further supported by the inhibitory effect on exocytosis in PC12 cells overexpressing IL1RAPL. Taken together, our data suggest that IL1RAPL may regulate calcium-dependent exocytosis and provide insight into the understanding of physiopathological mechanisms underlying cognitive impairment resulting from IL1RAPL dysfunction.
* To whom correspondence should be addressed. Tel: +33 144412410; Fax: +33 144412421; Email: chelly{at}cochin.inscrm.fr
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
A. Piton, J. L. Michaud, H. Peng, S. Aradhya, J. Gauthier, L. Mottron, N. Champagne, R. G. Lafreniere, F. F. Hamdan, S2D team, et al. Mutations in the calcium-related gene IL1RAPL1 are associated with autism Hum. Mol. Genet., December 15, 2008; 17(24): 3965 - 3974. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Gambino, A. Pavlowsky, A. Begle, J.-L. Dupont, N. Bahi, R. Courjaret, R. Gardette, H. Hadjkacem, H. Skala, B. Poulain, et al. IL1-receptor accessory protein-like 1 (IL1RAPL1), a protein involved in cognitive functions, regulates N-type Ca2+-channel and neurite elongation PNAS, May 22, 2007; 104(21): 9063 - 9068. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Hui, D. McHugh, M. Hannan, F. Zeng, S.-Z. Xu, S.-u.-H. Khan, R. Levenson, D. J. Beech, and J. L. Weiss Calcium-sensing mechanism in TRPC5 channels contributing to retardation of neurite outgrowth J. Physiol., April 1, 2006; 572(1): 165 - 172. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Brackmann, S. Schuchmann, R. Anand, and K.-H. Braunewell Neuronal Ca2+ sensor protein VILIP-1 affects cGMP signalling of guanylyl cyclase B by regulating clathrin-dependent receptor recycling in hippocampal neurons J. Cell Sci., June 1, 2005; 118(11): 2495 - 2505. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. A. Khan, E. K. Brint, L. A. J. O'Neill, and L. Tong Crystal Structure of the Toll/Interleukin-1 Receptor Domain of Human IL-1RAPL J. Biol. Chem., July 23, 2004; 279(30): 31664 - 31670. [Abstract] [Full Text] [PDF] |
||||




