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Transthyretin (TTR) has been proposed to have first evolved in reptiles and is one of the three plasma proteins important in the transport of thyroid hormones in higher vertebrates. A full-length cDNA encoding TTR was isolated from a sea bream (Sparus aurata) liver cDNA library using a homologous TTR cDNA probe generated by RT-PCR. Comparison of the deduced amino acid sequence of sea bream TTR with other published sequences, revealed an overall identity of 47-54%, although the amino acids in the active binding site were almost 100% conserved. Distribution of TTR was studied in sea bream adult tissue by RT-PCR and was detected in liver, brain, pituitary, gills, kidney, intestine and testis, although northern blot analysis only revealed TTR in the liver, suggesting that in sea bream, liver is the main source of this protein. TTR was also expressed in larvae from the first day post-hatch (48 h post-fertilisation). Analysis of thyroxine (T4) and triiodo-L-thyronine (T3) binding to sea bream serum proteins demonstrated that both T4 and T3 bind to albumin and TTR. By demonstrating the existence of TTR in teleost fish this study indicates TTR must have evolved in a common fish ancestor of the tetrapod evolutionary line.

Identification of Transthyretin in Fish (Sparus aurata): cDNA Cloning and Characterisation