The detection of the glial cell-line derived neurotrophic factor (GDNF
) mRNA by RT-PCR in dissociated cell culture of rat embryonic or post-
natal brain allowed the amplification of a doublet. The major band cor
responded to the expected size and the minor one to a shorter product.
We cloned and sequenced the latter product, and thus identified a mRN
A potentially encoding for an isoform of the initially described precu
rsor protein involved in GDNF synthesis.