In pulmonate molluscs two precursors for FMRFamide-related peptides (F
aRPs) are generated from a single gene by alternative splicing. One pr
ecursor gives rise to FMRFamide and FLRFamide and a few variants: the
tetra-FaRPs. A second precursor gives rise to heptapeptides of the for
m XDPFLRFamide and variants: the hepta-FaRPs. The tetra-FaRPs and hept
a-FaRPs have mutually exclusive cellular localizations and have some d
iffering actions on neurons and muscles. Hepta-FaRPs have been found i
n all pulmonates examined, even the most primitive species, but only i
n pulmonates and not other gastropods. A decapeptide FaRP isolated fro
m the mussel Mytilus-ALAGDHFFRFamide-is one of the more hepta-FaRP-lik
e peptides isolated from a non-pulmonate, and thus is a candidate homo
log of the hepta-FaRPs. But we show that this decapeptide is encoded o
n the same exon as FMRFamide in the mussel Geukensia, and thus is not
a real homolog of the hepta-FaRPs. Since the one and only FaRP precurs
or known from the opisthobranch Aplysia has a splice junction at a loc
ation similar to that of the tetra-FaRP precursor of pulmonates, we sp
eculated that an alternatively-spliced form of the FMRFamide gene exis
ts in this species too. One candidate was the precursor for a group of
peptides ending in LFRFamide, but we found that this precursor has no
significant sequence in common with the FMRFamide precursor. Thus, th
ere remains a dichotomy between pulmonates and all other molluscs with
regard to their FMRFamide genes and FMRFamide-related peptides.