Cloning, characterization, and expression of human LIG1

Biochem Biophys Res Commun. 2001 Jun 29;284(5):1155-61. doi: 10.1006/bbrc.2001.5092.

Abstract

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 and tumor suppressor in human tissues.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Chromosome Mapping
  • Chromosomes, Human, Pair 3*
  • Cloning, Molecular
  • DNA, Complementary / analysis
  • DNA, Complementary / metabolism
  • Gene Expression*
  • Humans
  • Karyotyping
  • Membrane Glycoproteins / genetics*
  • Molecular Sequence Data
  • Sequence Homology
  • Tissue Distribution

Substances

  • DNA, Complementary
  • LRIG1 protein, human
  • Membrane Glycoproteins