In the present study, the complete amino acid sequence of N-terminal procal
citonins (N-proCTs) of stingray tan elasmobranch) and spotlined sardine (a
teleost), as well as the partial amino acid sequence of N-proCTs of goldfis
h (a teleost; three types of N-proCTs) and bullfrog tan amphibian) have bee
n determined. These N-proCTs have some common features to 9 N-proCTs sequen
ced to date. These features were summarized as follows: 1) The first amino
acid residue is Ala or Val. 2) There is no Cys residue in the sequence of N
-proCTs. 3) Seven residues (Pro(3), Leu(19), Leu(28), Val(32), Gln(37), Gln
(45) and Ser(56)) are conserved in the sequence of N-terminal procalcitonin
(N-proCT), at least judging from the present data. 4) Insertion/deletion p
oints are present in the sequence of N-proCTs at the 2nd position, from the
10th to 14th and from 46th to 52nd. We examined whether the N-proCTs can b
e categorized into several groups by similarity of amino acid residues cons
erved in the molecules. Asa result, the N-proCTs were roughly categorized i
nto 2 groups: a mammalian group, including 2 subgroups and a non-mammalian
group, including 3 subgroups. This classification of N-proCTs coincides wit
h that of calcitonin. Sardine N-proCT has no accelerating effects on mitosi
s and cell differentiation of human osteosarcoma cells, as does the homolog
ous human N-proCT. Further studies are needed to elucidate the biological a
ctivity of N-proCTs.