Rm. Dores et S. Harris, DIFFERENTIAL N-ACETYLATION OF ALPHA-MSH AND BETA-ENDORPHIN IN THE INTERMEDIATE PITUITARY OF THE TURTLE, PSEUDEMYS-SCRIPTA, Peptides, 14(4), 1993, pp. 849-855
Steady-state analyses of the intermediate pituitary of the turtle, Pse
udemys scripta, indicated that alpha-MSH-sized immunoreactive forms an
d beta-endorphin-sized immunoreactive forms are major end products of
melanotropic cells. Three forms of alpha-MSH-related immunoreactivity
were detected. The two major forms had the same reversed-phase HPLC pr
operties as synthetic N,O-diacetyl-ACTH(1 - 13)-NH2 and N-acetyl-ACTH(
1 - 13)-NH2. These forms accounted for 97% of the total alpha-MSH-rela
ted immunoreactivity detected. A minor peak of ACTH(1 - 13)-NH2 was al
so detected. Multiple forms of beta-endorphin-related immunoreactivity
were detected, which varied in net positive charge (+1 to +5), appare
nt molecular weight (2.4 to 3.5 kDa), and degree of N-terminal acetyla
tion. Although N-acetylated forms of beta-endorphin were detected in t
he turtle intermediate pituitary, the major forms of turtle beta-endor
phin were nonacetylated. These features of the turtle intermediate pit
uitary POMC-specific N-acetylation mechanism are similar to, yet disti
nct from, the POMC N-acetylation mechanisms observed for mammals. Thes
e data suggest that POMC-specific N-acetylation mechanisms were presen
t in reptiles prior to the divergence of the anapsid and synapsid line
s.