Amino acid sequences of α-skeletal muscle actin isoforms in two species of rattail fish, Coryphaenoides acrolepis and Coryphaenoides cinereus

Abstract

The cDNA clones of α-skeletal actins were isolated from the skeletal muscle of two species of rattail fish, Coryphaenoides acrolepis and Coryphaenoides cinereus. The complete nucleotide sequences of the cDNA and their deduced amino acid sequences were determined. Each of the two species had two α-skeletal actin cDNA. The nucleotide sequences of the coding region of the two α-skeletal actin isoform genes within each species had 92.0 and 91.8% homology. From the cDNA sequences of the four α-skeletal actin isoforms in the two species, amino acid sequences of 377 amino acid residues were deduced. It was predicted that the two N-terminal amino acid residues of each protein are processed after translation. The amino acid sequences of α-skeletal actin 1 in the two Coryphaenoides species were identical, as were the amino acid sequences of α-skeletal actin 2 in the two species. The amino acid sequences of the two α-actin isoforms, α-skeletal actin 1 and α-skeletal actin 2, differed by only a single amino acid, Ala/Ser at the 155th position. Northern blot analysis showed that a similar amount of each of the two α-actin isoform mRNA was expressed in the skeletal muscle of the two Coryphaenoides species.