Cloning of a novel member of the low-density lipoprotein receptor family

被引:184
作者
Hey, PJ
Twells, RCJ
Phillips, MS
Nakagawa, Y
Brown, SD
Kawaguchi, Y
Cox, R
Xie, GC
Dugan, V
Hammond, H
Metzker, ML
Todd, JA
Hess, JF [1 ]
机构
[1] Merck Res Labs, Dept Human Genet, W Point, PA 19486 USA
[2] Univ Oxford, Nuffield Dept Surg, Wellcome Trust Ctr Human Genet, Oxford, England
基金
英国惠康基金;
关键词
diabetes; autoimmunity; polygenic disease; positional cloning; human genetics;
D O I
10.1016/S0378-1119(98)00311-4
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A gene encoding a novel transmembrane protein was identified by DNA sequence analysis within the insulin-dependent diabetes mellitus (IDDM) locus IDDM4 on chromosome 11q13. Based on its chromosomal position, this gene is a candidate for conferring susceptibility to diabetes. The gene, termed low-density lipoprotein receptor related protein 5 (LRP5), encodes a protein of 1615 amino acids that contains conserved modules which are characteristic of the low-density lipoprotein (LDL) receptor family. These modules include a putative signal peptide for protein export, four epidermal growth factor (EGF) repeats with associated spacer domains, three LDL-receptor (LDLR) repeats, a single transmembrane spanning domain, and a cytoplasmic domain. The encoded protein has a unique organization of EGF and LDLR repeats; therefore, LRP5 likely represents a new category of the LDLR family. Both human and mouse LRP5 cDNAs have been isolated and the encoded mature proteins are 95% identical, indicating a high degree of evolutionary conservation. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:103 / 111
页数:9
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