N-terminal amino acid sequences of three functionally different troponin T isoforms from rabbit fast skeletal muscle

Abstract

The different isoforms of fast skeletal muscle troponin T (TnT) are generated by alternative splicing of several 5′ exons in the fast TnT gene. In rabbit skeletal muscle this process results in three major fast TnT species, TnT 1f, TnT 2f and TnT 3f, that differ in a region of 30 to 40 amino acid residues near the N terminus. Differential expression of these three isoforms modulates the activation of the thin filament by calcium. To establish a basis for further structure-function studies, we have sequenced the N-terminal region of these proteins. TnT 2f is the fast TnT sequenced by Pearlstone et al.. The larger species TnT 1f contains six additional amino acid residues identical in sequence and position to those encoded by exon 4 in the rat fast skeletal muscle TnT gene. TnT 3f also contains that sequence but lacks 17 amino acid residues spanning the region encoded by exons 6 and 7 of the rat gene. These three TnTs appear to be generated by discrete alternative splicing pathways, each differing by a single event. Comparison of these TnT sequences with those from chicken fast skeletal muscle and bovine heart shows that the splicing pattern resulting in the excision of exon 4 is evolutionarily conserved and leads to a more calcium-sensitive thin filament.