Cloning, characterization, and expression of human LIG1

被引:122
作者
Nilsson, J
Vallbo, C
Guo, DS
Golovleva, I
Hallberg, B
Henriksson, R [1 ]
Hedman, H
机构
[1] Umea Univ, Dept Radiat Sci, SE-90187 Umea, Sweden
[2] Umea Univ, Dept Oncol, SE-90187 Umea, Sweden
[3] Umea Univ, Dept Clin Genet, SE-90187 Umea, Sweden
[4] Umea Univ, Dept Biol Mol, SE-90187 Umea, Sweden
关键词
LIG-1; 3p14; EGF; cancer; tumor suppressor; FISH; real-time PCR;
D O I
10.1006/bbrc.2001.5092
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Growth factor receptors are frequently amplified and over-expressed in various human cancers. Recently, a Drosophila cell surface protein, Kekkon-1, was found to participate in an epidermal growth factor (EGF) driven negative feedback loop. Kekkon-1 is induced by EGF, binds to the EGF-receptor, and inhibits receptor-mediated signaling. Here, we have searched for human genes with homologies to Kekkon-1 and identified human LIG1. The gene is the human homologue of mouse Lig-1 and is located on chromosome band 3p14, a region frequently deleted in various human cancers. It is predicted to encode a transmembrane cell-surface protein with extracellular leucine-rich repeats and immunoglobulin-like domains. LIG1 mRNA was detected in all tissues analyzed. The highest and lowest relative expression levels were found in brain and spleen, respectively, and differed by more than 200-fold. Taken together, our data are compatible with a role for LIG1 as a growth tumor suppressor in human tissues. (C) 2001 Academic Press.
引用
收藏
页码:1155 / 1161
页数:7
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