Hostname: page-component-848d4c4894-2xdlg Total loading time: 0 Render date: 2024-06-22T17:02:23.001Z Has data issue: false hasContentIssue false

Isolation, sequence, and chromosomal localisation of the human IκBR gene (NFKBIL2)

Published online by Cambridge University Press:  01 January 2000

D. A. M. NORMAN
Affiliation:
Cardiothoracic Surgery, National Heart & Lung Institute, Imperial College School of Medicine, Dovehouse Street, London SW3 6LY, UK
P. J. R. BARTON
Affiliation:
Cardiothoracic Surgery, National Heart & Lung Institute, Imperial College School of Medicine, Dovehouse Street, London SW3 6LY, UK
Get access

Abstract

THE INHIBITORS OF NF-κB (IκBs) play an important role in the regulation of the NF-κB pathway. IκBR (for IκB-Related) is proposed to be a novel member of this family. We report the cloning and characterization of the region of the human gene encoding the previously reported mRNA. This region contains 13 exons, spread over 6550 bp of genomic sequence. The coding sequence is only weakly similar to other IκBs and the exons display a more complicated structure than has been found in other members of the IκB gene family. Moreover, the positions of intron-exon junctions are different from those found in other IκB genes, even within the otherwise conserved ankyrin-like repeat region, suggesting that the IκBR gene is not a member of this extended gene family. We report a revised mRNA and protein sequence for IκBR, which predicts that the protein is larger than originally described. We also report the chromosomal localisation of the human IκBR gene (approved gene symbol NFKBIL2) to 8q24.3 using PCR-based somatic cell hybrid panel analysis and fluorescence in situ hybridization (FISH) mapping.

Type
Research Article
Copyright
© University College London 2000

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)