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J. Biol. Chem., Vol. 276, Issue 6, 4150-4157, February 9, 2001
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§,
§¶
**
From the Using differential display of rat fetal and
postnatal cardiomyocytes, we have identified a novel
seven-transmembrane receptor, ETL. The cDNA-predicted amino acid
sequence of ETL indicated that it encodes a 738-aa protein composed of
a large extracellular domain with epidermal growth factor (EGF)-like
repeats, a seven-transmembrane domain, and a short cytoplasmic tail.
ETL belongs to the secretin family of G-protein-coupled peptide hormone
receptors and the EGF-TM7 subfamily of receptors. The latter are
characterized by a variable number of extracellular EGF and cell
surface domains and conserved seven transmembrane-spanning regions. ETL
mRNA expression is up-regulated in the adult rat and human heart.
In situ hybridization analyses revealed expression in rat
cardiomyocytes and abundant expression in vascular and bronchiolar
smooth muscle cells. In COS-7 cells transfected with Myc-tagged rat
ETL, rat ETL exists as a stable dimer and undergoes endoproteolytic
cleavage of the extracellular domain. The proteolytic activity can be
abolished by a specific mutation, T455A, in this domain. In transfected mammalian cells, ETL is associated with cell membranes and is also
observed in cytoplasmic vesicles. ETL is the first seven-transmembrane receptor containing EGF-like repeats that is developmentally regulated in the heart.
Department of Human Genetics,
¶ Department of Internal Medicine, Division of Cardiology, and
Howard Hughes Medical Institute, § University of
Utah, Eccles Institute of Human Genetics,
Salt Lake City, Utah 84112
The nucleotide sequence(s) reported in this paper has been submitted to the GenBankTM/EMBL Data Bank with accession number(s) AF192401, AF192402, and AF192403.
** To whom correspondence should be addressed. Tel.: 617-355-2111; Fax: 617-730-8317; E-mail: mkeating@genetics.med.harvard.edu.This article has been cited by other articles:
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