The genomic organization of rat urocortin was determined using both cDNA an
d liver genomic DNA as templates for polymerase chain reactions. A single i
ntron of 261 bp was found upstream to the ATG start codon, and the whole ur
ocortin coding sequence was shown to be contained in a single exon. Relying
on these results, oligonucleotide primers were designed, which can differe
ntiate genomic DNA contamination from cDNA-derived signals in a reverse tra
nscription-polymerase chain reaction. Tissue screening for urocortin expres
sion revealed that the mid-brain is the major site of urocortin mRNA expres
sion, and that other peripheral organs, including lymphoid tissues and peri
pheral blood lymphocytes, do not produce urocortin. (C) 2000 Elsevier Scien
ce Ireland Ltd. All rights reserved.