The human C3a receptor (C3aR) mediates the activation of cells by the
potent proinflammatory chemoattractant C3a, an anaphylatoxin, generate
d in the early phase of an inflammatory reaction by proteolytic cleava
ge of the complement component C3. To understand the molecular mechani
sms that regulate C3aR gene expression, we initiated studies to determ
ine its genomic and mRNA organization. We now report the following nov
el findings: (1) The C3aR is a single-copy gene as shown by Southern h
ybridization of human genomic DNA. (2) Using PCR amplification of DNA
from monochromosomal somatic cell hybrid and radiation hybrid panels,
the C3aR locus was mapped to chromosome 12p13. (3) Genomic DNA clones
encompassing the C3aR locus were isolated from a human genomic DNA lib
rary and characterized by restriction mapping, Southern blotting, PCR
analysis and DNA sequencing. Comparison of the genomic with the known
cDNA sequences revealed a single similar to 6-kb intron sequence locat
ed 11 bp upstream of the ATG initiation codon. The open reading frame
and the complete 3' untranslated region are encoded on a single exon.